Literature DB >> 35239741

Chronic kidney disease and associated factors among adult population in Southwest Ethiopia.

Kindie Mitiku Kebede1, Dejene Derseh Abateneh1,2, Melkamu Beyene Teferi1, Abyot Asres1.   

Abstract

In Ethiopia, data on the burden and determinants of chronic kidney disease (CKD) in the general population is limited. This community-based study was conducted to assess the burden and associated factors of CKD among adults in Southwest Ethiopia. The study was conducted from August 23, 2018-October 16, 2018. Study participants were selected using a random sampling method. A structured questionnaire was used to collect relevant data. Blood pressure and anthropometric indices were measured following standard procedures. About 5 ml of urine sample was collected and the dipstick test was performed immediately. A blood sample of 3-5ml was collected for serum creatinine and blood glucose level determination. The three commonest estimators of glomerular filtration rate and the National Kidney Foundation Kidney Disease Outcomes Quality Initiative were used to define and stage CKD. Data were analyzed using SPSS 21. Multivariable logistic regression was employed and p-value <0.05 was used to indicate statistically significant results. A total of 326 participants with a mean age of 39.9(SD±11.2) years were enrolled in the study. The proportions of female participants (59.8%) were relatively higher than male participants (40.2%). The mean eGFR using CKD-EPI, CG and MDRD was 124.34 (SD±23.8) mL/min/1.73m2, 110.67(SD±33.0) mL/min/1.73m2 and 131.29 (SD±32.5) mL/min/1.73m2 respectively. The prevalence of CKD was 7.4% using CKD-EPI & MDRD and 8% using CG. Similar finding using CKD-EPI & MDRD may indicate that either CKD-EPI or MDRD can be used to estimate GFR in this study area. In the age and sex-adjusted logistic regression model, hypertension was significantly associated with CKD using CKD-EPI & MDRD and age ≥40 years old was significantly associated with CKD using CG. Behavioral characteristics and other traditional risk factors were not significantly associated with CKD in the current study. The prevalence of CKD was high in the study area. Only hypertension and age ≥40 years old were significantly associated with CKD. More of the increased prevalence of CKD in the current study remained unexplained and deserves further study.

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Year:  2022        PMID: 35239741      PMCID: PMC8893675          DOI: 10.1371/journal.pone.0264611

Source DB:  PubMed          Journal:  PLoS One        ISSN: 1932-6203            Impact factor:   3.240


Introduction

Chronic kidney disease (CKD) is among Non-communicable diseases (NCD) which cause significant morbidity and mortality globally [1]. A recent systematic review and meta-analysis estimated that the global pooled prevalence of CKD ranges from 11–13% and 13.9% prevalence in sub-Saharan Africa [2]. The epidemiology of CKD in sub-Saharan Africa is different from other regions that it mainly affects the economically productive young age group. The risk of CKD like HIV infection, hypertension, diabetes, and other infectious diseases are increasing in sub-Saharan Africa [2-5]. Although Ethiopia is among the countries that strive to achieve sustainable development goals 2016–2030, the progress towards the reduction of NCD associated deaths is limited. More than one third of, (39%) annual deaths are associated with NCD [6]. The burden of CKD is increasing and mainly associated with poor community awareness, insufficient data, and poor healthcare infrastructure [7]. In Ethiopia, studies that assess the prevalence and associated factors of CKD are very limited. The available studies are not representative because they are taken from high-risk groups, like, diabetes and HIV patients [7, 8]. A high prevalence of CKD, 18.2% and 23.8% using the Modification of Diet in Renal Disease (MDRD) and Cockcroft-Gault (C-G) equations respectively was reported among diabetic patients [7]. Owing to limited community based published reports available so far on CKD in Ethiopia, this study was conducted to assess the prevalence and associated factors of CKD among adults in Southwest Ethiopia.

Materials and methods

Study area, study design, and participants

A community-based cross-sectional study was conducted in the Sheka zone, Southern Nation, Nationality and People Region (SNNPR), Southwest Ethiopia. It is bordered on the South by Bench Maji, on the West by the Gambella region, on the North by the Oromia region and on the East by the Kaffa zone. The administrative center of Sheka is Masha which is located approximately 610 Km Southwest of Addis Ababa. Based on the 2007 census conducted by the central statistical agency, the zone had a total population of 199,314 of whom 101,059 were men and 98,255 were women. About 34, 2227 (17.17%) were urban inhabitants. The study was conducted from August 23, 2018 to October 16, 2018. The minimum sample size (N) was determined by using single population proportion formula [N = (Z α/2) 2 P (1-P) /d2], where Zα/2 = the value under standard normal table at 95% level of confidence which is 1.96, prevalence P, 15.2% prevalence of CKD among urban adults [9], margin of error d, which was set at 4%. Including a 10% non-response rate, the final sample size was 384 adults. Permanent residents aged ≥18 years in the households of Masha and Tepi town were included in the study. However, pregnant women and participants with acute illness with fever during data collection were excluded. Mentally disabled and those unable to give response were also excluded from the study.

Sampling procedure

A total of two urban areas of Sheka zone was selected randomly i.e. Tepi and Masha from a total of three urban areas (Tepi, Mash and Andracha). Tepi town had three kebeles, while Masha town had two kebeles during the study period. A total of 3 kebeles were randomly included in the study from a total of 5 kebeles in the selected urban areas. Then, the lists of households were taken from the administration of each kebele. All households in the selected urban kebeles with adults ≥18 years old were enumerated with the help of health extension workers to generate the sampling frame. After the generation of the sample framing, the sample size was allocated proportionally to the total household of each kebele. Finally, eligible participants were selected using a random sampling method. In the case of more than one adult population in a single household, one was selected using the lottery method. In case where eligible respondents were not available at the time of data collection, a revisit for three times was made. Respondents who were not available after three visits were considered as non-respondents.

Data collection and laboratory methods

A structured questionnaire adapted from various literatures [9-11] was used to collect data on socio-demographic, economic, behavioral and co-morbidity related characteristics of participants. Height, weight, blood pressure and waist circumference of all participants were measured by trained data collectors following standardized procedures. Blood pressure readings were performed using a digital blood pressure apparatus after the participant had remained in a sited position for three to five minutes on his or her right arm resting on the chair. Weight, height and waist circumference were measured in light clothing without shoe. Height was taken to the nearest 0.1 cm with a portable stadiometer (Seca 274, Germany) and weight was measured to the nearest 0.1k.g on mechanical Seca (Seca761, Germany). Waist circumference was measured using tape measures on the midway between the top of the hip bone and the bottom of the ribs. Participants were instructed to put off their heavy clothes and breathe out normally before waist circumference measurements. Waist circumference measurements were taken to the nearest 0.1cm. Blood pressure and all anthropometric measurements were made twice, and their averages were used in all analysis. About 5 ml random urine sample was collected using a clean, leak-proof urine cup for urine chemical analysis. Chemical analysis of urine specimens was performed immediately after sample collection using urine dipsticks test (Multistix® Henry Schein, Inc. https://www.henryschein.com/medical-multistix.aspx). Semi-quantitative chemical analysis of CKD markers (protein) was performed. Blood sample of 3–5 ml for serum creatinine and blood glucose level determination was collected using a syringe with needle and transferred to a gel containing serum separator test tube. Blood specimens were transported to the nearest general hospital (Tepi general hospital) for serum separation. A serum was separated after the sample clotted and centrifuged at 1000 – 2000g for 10 minutes by trained laboratory technologist. Serum sample was immediately separated from the whole blood and transferred to nunc tube. The serum was kept frozen at -20°C until processed and then transported on ice-cooled containers to Jimma teaching and referral hospital, Ethiopia for analysis. The creatinine and blood glucose levels were measured using the ABX pentra400 chemistry analyzer and reported in mg/dL or μmol/L (HORIBA, ABX, Japan). The ABX Pentra 400 is a multiparametric analyzer in which it has good reliability and practicability for routine and specialized clinical chemistry analyses, evaluated according to the National Committee for Clinical Laboratory Standards [12].

Variables’ definition

The three common equations were used to estimate glomerular filtration rate (eGFR), and the National Kidney Foundation Kidney Disease Outcomes Quality Initiative (NKF/KDOQI) guidelines to define and stage CKD [13]. We defined a participant as having CKD if he or she had GFR below 60 ml/min/1.73 m2 and/or had proteinuria (positive dipstick at least +1). Glomerular filtration rate classification was based on the following: stage 1: GFR > 90 with proteinuria; stage 2: GFR 60–89 with proteinuria; stage 3a: GFR 45–59; stage 3b: GFR 30–44; stage 4: GFR 15–29 and stage 5 end-stage renal disease (ESRD): GFR < 15 (Fig 1). Hypertension was defined as a systolic (SBP) ≥140 mmHg and/or a diastolic blood pressure of (DBP) ≥90 mmHg or self-reported on anti-hypertension drugs. Diabetes was defined as random blood sager >200mg/dl and/or self-reported on anti-hyperglycemic medication. A separate cut of points was used to level central obesity for men and women: women were leveled as central obese if their waist circumference was ≥88 cm and men were leveled as central obese if their waist circumference ≥102 cm.
Fig 1

Definitions and stages of chronic kidney disease [13].

The nutritional status of participants was assessed using body mass index (BMI) and leveled as follows: underweight: <18.5; normal weight: 18.5–24.9; overweight: 25–29.9 and obese: >30.

Traditional causes of CKD

Refer to the well-known causes of CKD such as hypertension, diabetes, obesity, and HIV.

Heart diseases

In this study, it means a self-reported history of heart diseases such as coronary disease (vessel surgery), or heart failure, or heart attack or stroke.

Moderate activities/exercise

Brisk walking or carrying light loads, gardening, household /domestic chores, roofing, painting for 30 minutes per day for five days a week.

Vigorous exercise/activity

Carrying or lifting heavy loads, digging or construction work, running, fast cycling, aerobics, fast swimming, playing football & volleyball for 30 minutes per day for five days a week.

Data analysis and interpretation

Data were entered into Epidata version 3.1 and exported to SPSS 21.0 for further analysis. Continuous data were presented as mean (± standard deviation) and categorical data as proportions. We used chi-square and fishers exact test for comparison of proportions and independent t-test for comparing mean differences. Logistic regression models were used to investigate the predictors of CKD. Variables with p-value of <0.2 in the bivariate analysis were included in the multivariable analysis. A p-values <0.05 were used to indicate statistically significant results.

Data quality control

Data collectors were trained and supervised during the data collection process. The questionnaire was first prepared in the English language and translated to the local language (Amharic). About 10% of the questionnaire was pretested among urban Kebeles of Sheka zone which were not included in this study before the actual study period. Completeness and consistency of the collected data were checked during data collection by the supervisors. Anthropometric equipment’s were calibrated frequently for every five measurements to control fallacy. Both intra-observer and interobserver variations were checked using SPSS version 21.0 during training of anthropometric measurement and the training was continued until an acceptable level of variation reached. Laboratory instruments were calibrated to guarantee reliability test result and laboratory tests were done according to manufacturer’s instructions, with their respective controls.

Ethics approval and consent to participate

Ethical approval was obtained from the ethics committee of Mizan Tepi University research directorate (Ref No: MTU/27/514/44/10). Permission of Sheka Zone, Southwest Ethiopia Health office and the head of the woreda were guaranteed. After explaining the objectives of the study, written consent was obtained from each study participant. For the participants who were not able to read and write, a fingerprint was used as a signature. The referral was considered for study participants with CKD and other medical risk factors.

Results

Socio-demographic characteristics

A total of 326 participants which gives a 95.9% response rate were included in this study. Most participants were within the age category of 18–39 (241; 73.9%) years. The proportions of female participants (59.8%) were relatively higher than male participants (40.2%). Significant differences in age, marital status and occupation were observed between male and females (p<0.05) as indicated in Table 1.
Table 1

Socio-economic and demographic characteristics of study participants in Sheka zone, Southwest Ethiopia, 2018.

CharacteristicsOverallMenWomenp-value
Age (Mean = 33.90 ± 11.2 years)0.011
18–39 years old241(73.9)87(66.4)154(79.0)
≥ 40 years old85(26.1)44(33.6)41(21.0)
Education status 0.163
Not attended formal education53(16.3)17(13.0)36(18.5)
Primary (1–8)116(35.6)42(32.1)74(37.9)
Secondary (9–12)90(27.6)44(33.6)46(23.6)
Above (12+)67(20.6)28(21.4)39(20.0)
Marital status 0.032
Married267(81.9)100(76.3)167(85.6)
Others*59(18.1)31(23.7)28(14.4)
Religion 0.477
Christian242(74.2)100(41.3)31(36.9)
Muslim84(25.8)142(58.7)53(63.1)
Occupation <0.001
Employed**53(16.3)22(16.8)31(15.9)
Farming56(17.2)37(28.2)19(9.7)
Merchant49(15.0)36(27.5)13(6.7)
Housewife104(31.9)3(2.3)101(51.8)
Students42(12.9)18(13.7)24(12.3)
Others***22(6.7)15(11.5)7(3.6)
Monthly income ((Median 2000(IQR = 2200 EB))0 .110
<2000EB113(34.7)38(36.9)75(46.9)
≥2000EB150(46.0)65(63.1)85(53.1)
Main source of water for drinking 0.771
Pip water171(52.5)70(53.4)101(51.8)
Wall/spring155(47.5)61(46.6)94(48.2)

EB = Ethiopian birr*Single, divorced or widowed ** Private and government employed ***house maid, retired, unemployed

EB = Ethiopian birr*Single, divorced or widowed ** Private and government employed ***house maid, retired, unemployed

Behavioral and Lifestyle characteristics

Majority of participants didn’t engage in vigorous activity/exercise (83.1%) or moderate activity/exercise (72.4%). A very small proportion (3.1%) of participants ever used herbal medicines. About 43 (13.2%) of the participants reported that they used nonsteroidal anti-inflammatory drugs. Nearly one-third of the participants (34.0%) reported that they drink <2 liters of water per day. A significant difference in alcohol and cigarette consumption, moderate exercise/activity, vigorous exercise/activity, and consumption of canned food between males and female were observed as described in Table 2.
Table 2

Behavioral related characteristics of study participants in Sheka zone, Southwest Ethiopia, 2018.

CharacteristicsOverallMenWomenP-value
Ever drink alcohol <0.001
Yes46(14.1)34(26.0)12(6.2)
No280(85.9)97(74.0)183(93.8)
Ever smoke cigarette
Yes17(5.2)17(13.0)0(0.0)
No309(94.8)114(87.0)195(100.0)
Smoking year 0.098
<10 years13(76.5)49(37.4)91(46.7)
≥10 years4(23.5)82(62.6)104(53.3)
Herbal medicine intake 0.326 #
Yes10(3.1)2(1.5%)8(4.1)
No316(96.9)129(98.5)187(95.9)
Vigorous exercise/activity 0.037
Yes55(16.9)29(22.1)26(13.3)
No271(83.1)102(77.9)169(86.7)
Moderate exercise/activity 0.013
Yes90(27.6)46(35.1)44(22.6)
No236(72.4)85(64.9)151(77.4)
Added salt to food 0.931
Never18(5.5)8(6.1)10(5.1)
Occasionally55(16.9)22(16.8)33(16.9)
With each meal253(77.6)101(77.1)152(77.9)
Eat canned/processed food <0.001
Never193(59.2)63(48.1)130(66.7)
Yes (occasionally and often)133(40.8)68(51.9)65(33.3)
Daily water intake
<2 letters per day111(34.0)46(35.1)65(33.3)0.739
≥ 2 letters per day215(66.0)85(64.9)130(66.7)
Use of over NSAIDs drugs regularly 0.002
Yes43(13.2)8(6.1)35(17.9)
No283(86.8)123(93.9)160(82.1)

# Fishers exact test was used

# Fishers exact test was used

Clinical characteristics/Co-morbidities

One fifth (21.1%; n = 71) of the participants were hypertensive: defined as being on antihypertensive drug or having a systolic blood pressure of ≥140mmHg and /or diastolic blood pressure of ≥ 90mmHg. Similarly, one-fifth of the participants (20.2%; n = 66) reported history of anemia. However, small proportion of the participants (3.4%; n = 11) were diabetic defined as being on drugs for diabetes and/or having blood glucose level >200mg/dl. Overall, there is a significant difference in the proportion of self-reported history of anemia and kidney stone between men and females (p<0.05) as described in Table 3.
Table 3

Clinical/co-morbidity related characteristics of study participants in Sheka zone, Southwest Ethiopia, 2018.

CharacteristicsOverallMenWomenP-value
Hypertension 0.215
Yes71(21.8)24(18.3)47(24.1)
No255(78.2)107(81.7)148(75.9)
Diabetes 0.761#
Yes11(3.4)5(3.8)6(3.1)
No315(96.6)126(96.2)189(96.9)
Anemia <0.001
Yes66(20.2)6(4.6)60(30.8)
No260(79.8)125(95.4)135(69.2)
Heart Disease * 0.374 #
Yes12(3.7)3(2.3)9(4.6)
No314(96.3)128(97.7)186(95.4)
Kidney stone 0.049
Yes34(10.4)19(14.5)15(7.7)
No292(89.6)112(85.5)180(92.3)

* Heart Disease includes coronary disease (vessel surgery), heart failure, or heart attack or stork, # Fishers exact test was used

* Heart Disease includes coronary disease (vessel surgery), heart failure, or heart attack or stork, # Fishers exact test was used

Anthropometric and laboratory measurements

Table 4 describes the mean differences of the anthropometric measurements and laboratory tests between men and women which were assessed using an independent t-test. A significant mean difference in height, BMI, serum creatinine, and eGFR using CKD-EPI and CG were observed between men and women (p<0.05). As expected, serum creatinine was higher in men than women (p < 0.001) but they had a significantly lower mean estimated creatinine clearance. We also found significantly high level of obesity among women as compared to men (p<0.001).
Table 4

Anthropometric and laboratory measurement results of study participants in Sheka zone, Southwest Ethiopia, 2018.

CharacteristicsOverallMenWomenP-value
Mean weight (Kg.) 60.96±9.6361.49± 9.1360.61±9.960.414
Mean height(meter) 1.60± 0.081.66±0.081.57±0.06<0.001
Mean SBP, mmHg (SD) 121.01±15.1121.14±12.5120.92±16.60.896
Mean DBP, mmHg (SD) 80.11± 10.779.30±9.280.66±11.60.262
Mean BMI, kg/m2 (SD) 23.84±4.1022.52±3.724.73±4.1<0.001
Mean serum creatinine, mg/dl (SD) 0.74±0.220.99±.310.69±.14<0.001
Mean creatinine clearance, ml/min (SD)
MDRD131.29±32.5114.79±37.6135.03±30.50.075
CG110.67±33.090.20±32.6115.32±32.70.033
CKD-EPI124.34±23.8107.10±33.3128.26±19.50.010
Obesity <0.001
Yes25(7.7)2(1.5)23(11.8)
No301(92.3)129(98.5)172(88.2)

Staging of kidney function and prevalence of chronic kidney disease

Using CKD-EPI estimator, about 23 (7.05%) of the participants had stage 1 and stage 2 CKD. Whereas, only 1 (0.3%) of them had chronic renal failure (stage 3a-5). The overall prevalence of CKD defined as proteinuria of ≥+1 and/or GFR<60 mL/min/1.73m2 was 7.4% ((95% confidence interval (CI) [4.6–10.4]). Using CG- estimator, about 21 (6.4%) of the participants had stage 1 and stage 2 CKD. Whereas, only 5 (1.5%) of them had chronic renal failure (stage 3a-5). The overall prevalence of CKD using CG-estimator and defined as proteinuria of ≥+1 and/or GFR <60 was 8.0% ((95% confidence interval (CI) [5.2–11.0]). whereas, using MDRD- estimator, about 23 (7.0%) of the participants had stage 1 and 2 CKD. Only 0.3% of them had chronic renal failure (stage 3a-5). The overall prevalence of CKD Using MDRD-estimator and defined as proteinuria of ≥+1and/or GFR<60 mL/min/1.73m2 was 7.4% ((95% confidence interval (CI) [4.6–10.1]) as showed in Table 5.
Table 5

Stages of kidney functions using the three eGFR estimators in Sheka zone, Southwest Ethiopia, 2018.

StagesGFR estimationCKD-Epi n (%)CG n (%)MDRD n (%)
1≥ 90, with proteinuria (≥+1)19(5.8)17(5.2)20(6.1)
260–89, with proteinuria (≥+1)4(1.2)4(1.2)3(0.9)
3a45–59.9, with or without proteinuria (≥+1)1(0.3)4(1.2)1(0.3)
3b30–44.9, with or without proteinuria (≥+1)0(0)1(0.3)0(0)
415–29.9, with or without proteinuria (≥+1)0(0)0(0)0(0)
5< 15, with or without proteinuria (≥+1)0(0)0(0)0(0)
Overall CKD24(7.4)26(8.0)24(7.4)

Bivariate and multivariable analysis of associated factors

As the outcome variable is dichotomous, we applied logistic regression model. Before applying the model, the assumptions of logistic regression were checked. The linear relationship between continuous independent variables (age and income) and their logit transformation were checked. We found that there was no linear relationship between age and income and their log transformations. As a result, we included age and income as categorical variables in the model. We also investigated the multicollinearity between independent variables using the variance inflation factor. A significant multicollinearity was not identified. We used three separate logistic regression models for three common GFR estimators. However, the models explained only up 41% (Nagelkerke R2) of the variance in the CKD. The Hosmer & Lemeshow test of the three models was not significant (p>0.05) which suggests good model fitness. Using all the three GFR estimators, age, hypertension, heart disease, central obesity and use of over the counter NSAIDs drugs regularly were significantly associated with CKD in the Bivariate analysis (p<0.05). In the full adjusted model, only hypertension was significantly associated with CKD using CKD-EPI & MDRD- estimators described in Tables 6 and 7 respectively. On the other hand, age was significantly associated with CKD using CG- estimator in the full adjusted model as describe in Table 8. Using CKD-EPI & MDRD- estimators, participants who had hypertension were nearly 2.61 times more likely to have CKD than those who didn’t have hypertension (p<0.001). Using CG- estimator, participants whose age ≥40 were 3.187 times more likely to exhibit CKD than whose age was 18–39 years (p = 0.005). However, central obesity and age showed borderline significant using CKD-EPI & MDRD estimators described in Tables 6 and 7 respectively.
Table 6

Factors associated with CKD in age and sex adjusted logistic regressions using CKD-EPI estimator in Sheka Zone, Southwest Ethiopia, 2018.

VariablesChronic Kidney DiseaseCOR with 95% CIP valueAOR with 95% CI
Socio-demographic characteristicsYes (n, %)No (n, %)
Sex
Male6(25.0)125(41.4)11
Female18(75.0)177(58.6)2.12(0.82–5.49)0.1221.031(0.295–3.598)
Age
18–3913(54.2)228(75.5)1
≥4011(45.8)74(24.5)2.607(1.120–6.067)0.0262.347(0.902–6.109)
Education status
Not attended formal education1(4.2)52(17.2)0.642(0.277–1.492)0.303
Attended formal education23(95.8)250(82.8)1
Marital status
Married21(87.5)246(81.5)1
Others3(12.5)56(18.5)0.628(0.181–2.177)0.463
Religion
Christian17(70.8)225(74.5)1
Muslim7(29.2)77(25.5)1.203(0.481–3.012)0.693
Occupation
Employed*4(7.5)49(92.5)
Farming2(3.6)54(96.4)0.454(0.080–2.587)0.374
Merchant4(8.2)45(91.8)1.089(0.257–4.613)
Housewife11(10.6)93(89.4)1.449(0.438–4.789)
Students2(4.8)40(95.2)0.613(0.107–3.518)
Others**1(4.5)21(95.5)0.583(0.061–5.535)
Ethnicity
Sheka (natives)9(37.5)77(25.5)1.753(0.737–4.168)0.204
Others***15(62.5)225(74.5)1
Monthly income
<2000EB9(45.0)104(42.8)1
≥2000EB11(55.0)139(57.2)0.914(0.366–2.287)0.848
Main source of water for drinking
Wall/spring11(45.8)144(47.7)0.928(0.403–2.138)0.861
Pip water13(54.2)158(52.3)1
Lifestyle/behavioral characteristics
Ever drink alcohol
Yes1(4.2)45(14.9)0.248(0.033–1.885)0.1780.269(0.033–2.176)
No23(95.8)257(85.1)1
Ever smoke cigarette
Yes1(4.2)16 5.3%0.777(0.099–6.125)0.811
No23(95.8)286(94.7)1
Smoking year
<10 years0(0.0)13(81.3)≅0.999
≥10 years1(100.0)3(18.8)1
Herbal supplement/ medicine
Yes2(8.3)8(2.6)3.341(0.669–16.696)0.1420.997(0.150–6.621
No22(91.7)294(97.4)1
Use of over the counter NSAIDs drugs regularly
Yes7(29.2)36(11.9)3.042(1.181–7.840)0.0212.219(0.760–6.483
No17(70.8)266(88.1)1
Vigorous exercise /activity
Yes2(8.3)53(17.5)0.427(0.097–1.8720.259
No22(91.7)249(82.5)1
Moderate exercise/activity
Yes9(37.5)81(26.8)1.637(0.689–3.887)0.264
No15(62.5)221(73.2)1
Eat canned/processed foods
Never13(54.2)180(59.6)1
Yes (occasionally and often)11(45.8)122(40.4)1.248(0.542–2.878)0.603
Added salt to food
Never1(4.2)17(5.6)0.871(0.109–6.970)0.878(0.096–8.007)
Occasionally7(29.2)48(15.9)2.160(0.843–5.534)0.1091.593(0.546–4.647
With each meal16(66.7)237(78.5)1
Daily water intake
<2 letters per day11(45.8)100(33.1)1.709(0.739–3.951)0.210
≥ 2 letters per day13(54.2)202(66.9)1
Co-morbidities/clinical characteristics
Hypertension
Yes12(50.0)59(19.5)4.119(1.762–9.629)0.0012.614(1.016–6.727
No12(50.0)243(80.5)1
Diabetes mellitus
Yes1(4.2)10(3.3)1.270(0.156–10.357)0.824
No23(95.8)292(96.7)1
Anemia
Yes6(25.0)60(19.9)1.344(0.512–3.5330.548
No18(75.0)242(80.1)1
Heart Disease*
Yes3(12.5)9(3.0)4.651(1.170–18.479)0.0292.539(0.456–14.142
No21(87.5)293(97.0)1
Kidney stone
Yes4(16.7)30(9.9)1.813(0.581–5.657)0.305
No20(83.3)272(90.1)1
Central obesity
Yes13(54.2)69(22.8)3.991(1.711–9.306)0.0012.352(0.770–7.188
No11(45.8)233(77.2)1
Nutritional status based on BMI
Under weight0(0.0)26(8.8)≅0
Normal weight15(62.5)175(58.9)0.986(0.212–4.589)
Overweight7(29.2)73(24.6)1.103(0.214–5.684)0.907
Obese2(8.3)23(7.7)1
Table 7

Factors associated with CKD in age and sex adjusted logistic regressions using MDRD estimator in Sheka Zone, Southwest Ethiopia, 2018.

VariablesChronic Kidney DiseaseCOR with 95% CIP valueAOR with 95% CI
Socio-demographic characteristicsYes (n, %)No (n, %)
Sex
Male6(25.0)125(41.4)11
Female18(75.0)177(58.6)2.119(0.818–5.489)0.1221.031(0.295–3.598)
Age
18–3913(54.2)228(75.5)1
≥4011(45.8)74(24.5)2.607(1.120–6.067)0.0262.347(0.902–6.109)
Education status
Not attended formal education1(4.2)52(17.2)0.209(0.028–1.582)0.303
Attended formal education23(95.8)250(82.8)1
Marital status
Married21(87.5)246(81.5)1
Others3(12.5)56(18.5)0.628(0.181–2.177)0.463
Religion
Christian17(70.8)225(74.5)1
Muslim7(29.2)77(25.5)1.203(0.481–3.012)0.693
Occupation
Employed*4(16.7)49(16.2)
Farming2(8.3)54(17.9)0.454(0.080–2.587)0.374
Merchant4(16.7)45(14.9)1.089(0.257–4.613)
Housewife11(45.8)93(30.8)1.449(0.438–4.789)
Students2(8.3)40(13.2)0.613(0.107–3.518)
Others**1(4.2)21(7.0)0.583(0.061–5.535)
Ethnicity
Sheka(natives)9(37.5)77(25.5)1.753(0.737–4.168)0.204
Others***15(62.5)225(74.5)11
Monthly income
<2000EB9(45.0)104(42.8)11
≥2000EB11(55.0)139(57.2)0.914(0.366–2.287)0.848
Main source of water for drinking
Wall/spring11(45.8)144(47.7)0.928(0.403–2.138)0.861
Pip water13(54.2)158(52.3)11
Lifestyle/behavioral characteristics
Ever drink alcohol
Yes1(4.2)45(14.9)0.248(0.033–1.885)0.1780.269(0.033–2.176)
No23(95.8)257(85.1)11
Ever smoke cigarette
Yes1(4.2)16(5.3)0.777(0.099–6.125)0.811
No23(95.8)286(94.7)1
Smoking year
<10 years0(0.0)13(81.3)≅00.999
≥10 years1(100.0)3(18.8)1
Herbal supplements medicine
Yes2(8.3)8(2.6)3.341(0.669–16.696)0.1420.997(0.150–6.621)
No22(91.7)294(97.4)11
Use of over the counter NSAIDs drugs regularly
Yes7(29.2)36(11.9)3.042(1.181–7.840)0.0212.219(0.760–6.483)
No17(70.8)266(88.1)11
Vigorous exercise /activity
Yes2(8.3)53(17.5)0.427(0.097–1.872)0.259
No22(91.7)249(82.5)1
Moderate exercise/activity
Yes9(37.5)81(26.8)1.637(0.689–3.887)0.264
No15(62.5)221(73.2)1
Eat canned/processed foods
Never13(54.2)180(59.6)1
Yes (occasionally and often)11(45.8)122(40.4)1.248(0.542–2.878)0.603
Added salt to food
Never1(4.2)17(5.6)0.871(0.109–6.970)0.878(0.096–8.007)
Occasionally7(29.2)48(15.9)2.160(0.843–5.534)0.1091.593(0.546–4.647)
With each meal16(66.7)237(78.5)11
Daily water intake
<2 letters per day11(45.8)100(33.1)1.709(0.739–3.951)0.210
≥ 2 letters per day13(54.2)202(66.9)1
Co-morbidities/clinical characteristics
Hypertension
Yes12(50.0)59(19.5)4.119(1.762–9.629)0.0012.614(1.016–6.727)
No12(50.0)243(80.5)11
Diabetes
Yes1(4.2)10(3.3)1.270(0.156–10.357)0.824
No23(95.8)292(96.7)1
Anemia
Yes6(25.0)60(19.9)1.344(0.512–3.533)0.548
No18(75.0)242(80.1)1
Heart Disease*
Yes3(12.5)9(3.0)4.651(1.170–18.479)0.0292.539(0.456–14.142)
No21(87.5)293(97.0)11
Kidney stone
Yes4(16.7)30(9.9)1.813(0.581–5.657)0.305
No20(83.3)272(90.1)1
Central Obesity
Yes(obese)13(54.2)69(22.8)3.991(1.711–9.306)0.0012.352(0.770–7.188)
No (not obese)11(45.8)233(77.2)11
Nutritional status based on BMI
Under weight0(0.0)26(8.8)≅0
Normal weight15(62.5)175(58.9)0.986(0.212–4.589)
Overweight7(29.2)73(24.6)1.103(0.214–5.684)0.907
Obese2(8.3)23(7.7)1
Table 8

Factors associated with CKD in age and sex adjusted logistic regressions using CG estimator in Sheka Zone, Southwest Ethiopia, 2018.

VariablesChronic Kidney DiseaseUnadjustedP-valueAdjusted
Socio-demographic characteristicsYes (n, %)No n, %)
Sex
Male6(23.1)125(41.7)11
Female20(76.9)175(58.3)2.381(0.929–6.100)0.0711.340(0.404–4.442)
Age
18–3913(50.0)228(76.0)1
≥4013(50.0)72(24.0)3.167(1.404–7.141)0.0053.187(1.281–7.926)
Education status
Not attended formal education2(7.7)51(17.0)0.407(0.093–1.776)0.232
Attended formal education24(92.3)249(83.0)11
Marital status
Married23(88.5)244(81.3)11
Others3(11.5)56(18.7)0.568(0.165–1.959)0.371
Religion
Christian18(69.2)224(74.7)11
Muslim8(30.8)76(25.3)1.310(0.547–3.135)0.544
Occupation
Employed*4(15.4)49(16.3)1
Farming3(11.5)53(17.7)0.693(0.148–3.256)
Merchant4(15.4)45(15.0)1.089(0.257–4.613)0.438
Housewife12(46.2)92(30.7)1.598(0.489–5.218)
Students2(7.7)40(13.3)0.613(0.107–3.518)
Others**1(3.8)21(7.0)0.583(0.061–5.535)
Ethnicity
Sheka (natives)10(38.5)76(25.3)1.842(0.802–4.232)0.150
Others***16(61.5)224(74.7)11
Monthly income
<2000EB11(50.0)102(42.3)11
≥2000EB11(50.0)139(57.7)0.734(0.306–1.758)0.488
Main source of water for drinking
Wall/spring13(50.0)142(47.3)1.113(0.499–2.480)0.794
Pip water13(50.0)158(52.7)11
Lifestyle/behavioral characteristics
Ever drink alcohol
Yes1(3.8)45(15.0)0.227(0.030–1.715)0.1510.253(0.032–2.025)
No25(96.2)255(85.0)1
Ever smoke cigarette
Yes1(3.8)16(5.3)0.710(0.090–5.578)0.745
No25(96.2)284(94.7)1
Smoking year
<10 years0(0.0)13(81.3)≅00.999
≥10 years1(100.0)3(18.8)1
Herbal supplements /medicine
Yes2(7.7)8(2.7)3.042(0.611–15.132)0.1741.106(0.167–7.342)
No24(92.3)292(97.3)1
Use of over the counter NSAIDs drugs regularly
Yes7(26.9)36(12.0)2.702(1.062–6.875)0.0371.937(0.673–5.576)
No19(73.1)264(88.0)1
Vigorous exercise /activity
Yes2(7.7)53(17.7)0.388(0.089–1.694)0.208
No24(92.3)247(82.3)1
Moderate exercise/activity
Yes10(38.5)80(26.7)1.719(0.749–3.944)0.201
No16(61.5)220(73.3)1
Eat canned/processed foods
Never15(57.7)178(59.3)1
Yes (occasionally and often)11(42.3)122(40.7)1.070(0.475–2.409)0.870
Added salt to food
Never1(3.8)17(5.7)0.768(0.097–6.104)0.716(0.078–6.543)
Occasionally7(26.9)48(16.0)1.904(0.754–4.809)0.1731.471(0.511–4.233)
With each meal18(69.2)235(78.3)1
Daily water intake
<2 letters per day11(42.3)100(33.3)1.467(0.650–3.311)0.357
≥ 2 letters per day15(57.7)200(66.7)1
Co-morbidities/clinical
Hypertension
Yes12(46.2)59(19.7)3.501(1.539–7.965)0.0032.105(0.836–5.299)
No14(53.8)241(80.3)1
Diabetes
Yes1(3.8)10(3.3)1.160(0.143–9.433)0.890
No25(96.2)290(96.7)1
Anemia
Yes6(23.1)60(20.0)1.200(0.462–3.119)0.708
No20(76.9)240(80.0)1
Heart Disease*
Yes3(11.5)9(3.0)4.217(1.068–16.661)0.0402.555(0.462–14.133)
No23(88.5)291(97.0)1
Kidney stone
Yes4(15.4)30(10.0)1.636(0.529–5.066)0.393
No22(84.6)270(90.0)1
Central Obesity
Yes14(53.8)68(22.7)3.980(1.758–9.011)0.0012.147(0.748–6.162)
No12(46.2)232(77.3)1
Nutritional status based on BMI
Under weight1(3.8)25(8.5)0.460(0.039–5.418)0.537
Normal weight15(57.7)175(59.3)0.986(0.212–4.589)
Overweight8(30.8)72(24.4)1.278(0.253–6.451)
Obese2(7.7)23(7.8)1

Discussion

In the current study, we assessed the prevalence and associated risk factors of chronic kidney diseases among the urban adult population in Sheka zone using the three commonest estimators of kidney functions. Over 7% of urban adults had CKD regardless of whether CKD-EPI, CG or MDRD GFR estimators were used. This finding is comparable with the prevalence of CKD reported in other sub-Saharan African counties; 10.4% in Nigeria [14], 12.4% in Kinshasa Congo [15], 10% in Cameroon [10], and 7% in Tanzania with 15.2% in the urban population [16]. The prevalence of CKD was slightly higher using the CG GFR estimator. It has been documented that CG overestimates the true prevalence of CKD [10, 16]. But, a similar prevalence of CKD was estimated using CKD-EPI and MDRD estimators. This may indicate that either CKD-EPI or MDRD can be used to estimate GFR in this study area. Other study findings, for instance, in Southern Africa and Ghana also showed that there is a high agreement between these two GFR estimators [17, 18]. Using NKF/KDOQI staging, we found that most of the participants were in stage I & II. The finding is in line with several study findings in developing countries [9-11]. People within the early stage of CKD may not aware of their status. In fact, several studies showed that the majority of CKD patients don’t aware their kidney problems [15, 19, 20]. Identification of people in the early stage of CKD is important. This is because the cardiovascular risks associated with stage I & II is nearly equal to that of stage III [21]. After adjusting socio-demographic, lifestyle and co-morbidities related variables, only hypertension and advanced age were found to be significantly associated with CKD using CKD-EPI/MDRD & CG estimators respectively. However, more of the increased prevalence of CKD in this study area seems to be unexplained. In line with our study finding, a recent study finding in Tanzania and Uganda showed that the majority of the increase in the risk of CKD was not explained [9, 11]. Unexplained risk factors of CKD in this study area may suggest that other non-traditional risk factors might contribute to the high burden of CKD. Some study findings in another part of the world showed that nontraditional risk factors such as heavy metals and agro-chemicals may contribute to CKD in tropical and semi-tropical areas [22, 23]. Some other studies suggested that infectious diseases such as HIV/AIDS, Schistosomiasis and Leishmaniasis are also associated with CKD [24-26]. However, as a limitation of this study, we didn’t control the confounding effect of these risk factors of CKD. Large-scale epidemiological studies are needed to better understand the specific risk factors of CKD and, to examine the potential but unmeasured above risk factors. As documented in the broad literature [7, 10, 11, 19], advanced age is a well-known risk factor of CKD. As age increases, there may be salt sensitization, hardening of arteries and scarring of the tiny blood vessels in the kidney. This may, in turn, enhance protein excretion and decrease GFR [27-29]. However, as many of the adult participants in the current study didn’t have a birth certificate, they may underestimate their age. Underestimation of age could lead to overestimation of GFR using any of the methods used to calculate GFR. This may in turn underestimate the true prevalence of CKD in this study area since the level of creatinine is affected by socio-demographic factors such as age [30]. In the current study, among the traditional risk factors of CKD, hypertension was found to be significantly associated with CKD. This is in line with several community-based study findings [10, 11, 14, 20]. Hypertension may elevate intraglomerular pressure which results in glomerulosclerosis and eventual protein trafficking [31, 32]. However, as a limitation of this study (chicken egg dilemma), it is hard to distinguish whether hypertension causes CKD or CKD causes hypertension. An increased risk of CKD among hypertensive participants may warrant urban adults to adhere to treatment and control their blood pressures. Studies have shown that interventions that decrease blood pressure levels in patients with proteinuria delay progression to CKD [33, 34]. Co-morbidity related factors such as diabetes, anemia, kidney stone; heart disease, central obesity and nutritional status measured by BMI were not significantly associated with CKD. However, central obesity showed a borderline significant. It has been documented that waist circumference or waist to hip ratio predicts cardiovascular risks than BMI [35]. The low prevalence of the above-mentioned co-morbidities in our participants makes any comment of their association difficult to ascertain. In the current study, behavioral factors such as alcohol intake and cigarette smoking were not significantly associated with CKD. This is in line with several study findings [14, 36, 37]. Alcohol intake and cigarette smoking are often considered anti-social habits in Ethiopia so people may give a negative response. This may, in turn, nullify the true association between alcohol intake, cigarette smoking and, CKD. Overall, in this study area, CKD is significantly associated with age ≥40 years old and hypertension. Early screening of high-risk populations (elderly and hypertensive peoples in the case of this study area) may help to diagnose people at the early stage of CKD. This is very important as Ethiopian health care institutions may not be able to support the economic burden of providing dialysis and renal replacement therapy to all patients. Dialysis and renal replacement therapy are not free in Ethiopia. This may result catastrophic out of the pocket expenditure. Thus, early screening of high-risk populations to CKD is important to minimize complications and out of pocket expenditures. This study was the first community-based assessment of CKD in Southwest Ethiopia using the three common GFR estimators. The finding of the study will provide information about the urban prevalence of CKD in Sheka zone. However, this study has several limitations. The cross-sectional nature of this study restricted us to infer causality. The common GFR measures used in this study were not validated in Ethiopia. The absence of reliable and validated measures of kidney function tests has made difficult the estimation of CKD in Africa [16, 18]. This study exclusively focused on the urban population. Thus, the estimated CKD may not reflect the prevalence and risk factors of rural communities. Because of security and financial restrictions, we didn’t make a three months control of positive findings as suggested by the KDIGO guideline. Some risk factors identified elsewhere such as heavy metals, agrochemicals, Schistosomiasis, Leishmaniasis and HIV [22-26] were not investigated in this study.

Conclusions

The prevalence of CKD was high in the study area. Only hypertension and age ≥ years old were significantly associated with CKD. More of the increased prevalence of CKD in the current study remained unexplained and deserves further study. Policymakers and programmers need to design strategies and encourage high-risk populations to be screened as early as possible. It is better if clinicians should also consider kidney function marker tests for hypertensive and patients older than 40 years old.

Questionnaire in English and local language (Amharic).

(PDF) Click here for additional data file. (SAV) Click here for additional data file.

Transfer Alert

This paper was transferred from another journal. As a result, its full editorial history (including decision letters, peer reviews and author responses) may not be present. 22 Jun 2020 PONE-D-20-08526 Chronic Kidney Disease and Associated factors among adult population in Southwest Ethiopia PLOS ONE Dear Dr. Abateneh, Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process. We recommend to include the potential impact of the kebeles in the results of the survey. We requiere to supress these first lines and start the paper directly with the CKD. Authors are required to re-define what advanced age means or modify the age ranges. > 40 years cannot be considered advanced age The increased prevalence of CKD in the current study remains unexplained and scarcely discussed. Authors are requiered to recommend the use of CKD-EPI, MDRD or CG to estimate CKD prevalence in order to make recommendations. The paper is suitable for publication but needs to focus in the novelty and originality of the studied population. We do not identify  any conflicts of interest. Please submit your revised manuscript by July 10th. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at plosone@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file. Please include the following items when submitting your revised manuscript: A rebuttal letter that responds to each point raised by the academic editor and reviewer(s). You should upload this letter as a separate file labeled 'Response to Reviewers'. A marked-up copy of your manuscript that highlights changes made to the original version. You should upload this as a separate file labeled 'Revised Manuscript with Track Changes'. An unmarked version of your revised paper without tracked changes. You should upload this as a separate file labeled 'Manuscript'. If you would like to make changes to your financial disclosure, please include your updated statement in your cover letter. Guidelines for resubmitting your figure files are available below the reviewer comments at the end of this letter. If applicable, we recommend that you deposit your laboratory protocols in protocols.io to enhance the reproducibility of your results. Protocols.io assigns your protocol its own identifier (DOI) so that it can be cited independently in the future. For instructions see: http://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols We look forward to receiving your revised manuscript. Kind regards, Domingo Gonzalez-Lamuño, Ph.D:, M.D. Academic Editor PLOS ONE Additional Editor Comments: There are similar papers as Sumaili et al in 2009 about prevalence of Chronic Kidney Disease in the Democratic Republic of Congo. Although there is no significant new clinical data, the study is based in a survey and there are some socio demographic data that are of interest. The survey is based in an administrative Ethiopian distribution of kebeles, making it original. However these points are not discussed along the paper. It would be of interest to compare the urban and rural areas. Moreover, the introduction is initially focused in the global burden of noncommunicable diseases (NCD) but this not the main point along the paper. Hypertension and advanced age were significantly associated with the excess risk of CKD, however the advanced age criteria is > 40 years. Authors must re-define what advanced age means or modify the age ranges. The increased prevalence of CKD in the current study remains unexplained and scarcely discussed. Authors must recommend the use of CKD-EPI, MDRD or CG to estimate CKD prevalence in order to make recommendations. The paper is suitable for publication but needs to focus in the novelty and originality of the studied population. There are no conflicts of interest. I consider that after this corrections in the introduction (eliminate the initial lines related to NCD, and start with CKD prevalence and the collected data related with general and CKD populations Journal Requirements: When submitting your revision, we need you to address these additional requirements. 1. Please ensure that your manuscript meets PLOS ONE's style requirements, including those for file naming. The PLOS ONE style templates can be found at https://journals.plos.org/plosone/s/file?id=wjVg/PLOSOne_formatting_sample_main_body.pdf and https://journals.plos.org/plosone/s/file?id=ba62/PLOSOne_formatting_sample_title_authors_affiliations.pdf 2. If you developed a questionnaire as part of this study and it is not under a copyright more restrictive than CC-BY, please include a copy, in both the original language and English, as Supporting Information. [Note: HTML markup is below. Please do not edit.] Reviewers' comments: [NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.] While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step. 27 Jul 2020 Ref No: PONE-D-20-08526 Title: Chronic Kidney Disease and Associated Factors among Adult Population in Southwest Ethiopia Response to reviewers 1. We recommend to include the potential impact of the kebeles in the results of the survey. Response: Dear reviewer, all the kebeles included in this study were urban kebeles and assumed to be homogenous. Therefore, the prevalence of CKD is not expected to vary among the included kebeles. 2. We require to suppress these first lines and start the paper directly with the CKD. Response: We have deleted the first paragraph and started the paper directly with the CKD (Introduction section, page 2, line 38-44). 3. Authors are required to re-define what advanced age means or modify the age ranges. > 40 years cannot be considered advanced age Response: Dear reviewer thank you very much for this comment. We couldn’t find a standard definition for advanced age for sub-Saharan countries. For this reason, we have removed the term “advanced age” and simply we categorized age as ≥40 years old and <40 years old. The age category was decided for comparison (Compare with other studies) (Abstract section, page 2, line 30; Discussion section, page 25, line 316; Conclusions section, page 26, line 337and 341). 4. The increased prevalence of CKD in the current study remains unexplained and scarcely discussed. Authors are required to recommend the use of CKD-EPI, MDRD or CG to estimate CKD prevalence in order to make recommendations. Response: Even though the aim of this study is not to recommend the use of CKD-EPI, MDRD or CG, we have incorporated recommendations on the use of CKD-EPI, MDRD, or CG to estimate CKD prevalence in this study area (Abstract section, page 2, line 27-28). 5. The paper is suitable for publication but needs to focus in the novelty and originality of the studied population. Response: Dear reviewer, thank you for this comment. At this stage, we can’t change the study population. It is difficult to say that the study population is unique. This study was conducted among the urban population in the Sheka zone. Therefore, the population may share similar characteristics with other urban populations in Ethiopia. However, this study is the first community-based study in the study area and in Ethiopia at large. In fact, this study has certain limitations. We have included those limitations in the manuscript. Response to Editor 1. There are similar papers as Sumaili et al in 2009 about prevalence of Chronic Kidney Disease in the Democratic Republic of Congo. Although there is no significant new clinical data, the study is based in a survey and there are some socio-demographic data that are of interest. The survey is based in an administrative Ethiopian distribution of kebeles, making it original. However, these points are not discussed along the paper. Response: Dear editor, all the kebeles included in this study were urban kebeles and assumed to be homogenous. Therefore, the prevalence of CKD is not expected to vary among the included kebeles. 2. It would be of interest to compare the urban and rural areas. Response: Dear editor, this study was exclusively studied in urban areas. Therefore, it is difficult to compare urban and rural areas. 3. Moreover, the introduction is initially focused in the global burden of noncommunicable diseases (NCD) but this not the main point along the paper. Response: We have deleted the first paragraph and started the paper directly with the CKD (page 2, line 38-44). 4. Hypertension and advanced age were significantly associated with the excess risk of CKD, however the advanced age criteria is > 40 years. Authors must re-define what advanced age means or modify the age ranges. Response: Dear editor, thank you very much for this comment. We couldn’t find a standard definition for advanced age for sub-Saharan countries. For this reason, we removed the term “advanced age” and simply we categorized age as ≥ 40 years old and <40 years old. The age category was decided for comparison (Compare with other studies) (Abstract section, page 2, line 30; Discussion section, page 25, line 316; Conclusions section, page 26, line 337 and 341). 5. The increased prevalence of CKD in the current study remains unexplained and scarcely discussed. Authors must recommend the use of CKD-EPI, MDRD or CG to estimate CKD prevalence in order to make recommendations. Response: Even though the aim of this study is not to recommend the use of CKD-EPI, MDRD, or CG, we have incorporated recommendation on use of CKD-EPI, MDRD or CG to estimate CKD prevalence in this study area (page 2, line 27-28) 6. The paper is suitable for publication but needs to focus in the novelty and originality of the studied population. Response: Dear editor, thank you for this comment. At this stage, we can’t change the study population. It is difficult to say that the study population is unique. This study was conducted among the urban population in the Sheka zone. Therefore, the population may share similar characteristics with other urban populations in Ethiopia. However, this study is the first community-based study in the study area and in Ethiopia at large. In fact, this study has certain limitations. We have included those limitations in the manuscript. 7. I consider that after this correction in the introduction (eliminate the initial lines related to NCD, and start with CKD prevalence and the collected data related with general and CKD populations Response: Corrected based on your comment. 8. If you developed a questionnaire as part of this study and it is not under a copyright more restrictive than CC-BY, please include a copy, in both the original language and English, as Supporting Information. Response: We have uploaded a questionnaire both in English and local language (Amharic) as supporting information. Submitted filename: Response to Reviewers.docx Click here for additional data file. 30 Jun 2021 PONE-D-20-08526R1 Chronic Kidney Disease and Associated Factors among Adult Population in Southwest Ethiopia PLOS ONE Dear Dr. Derseh, Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process. The reviewers have identified several aspects of your study design that require further clarification. Please ensure that you attend carefully to each of their queries when preparing a revised version of your manuscript. Please submit your revised manuscript by Aug 13 2021 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at plosone@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file. Please include the following items when submitting your revised manuscript: A rebuttal letter that responds to each point raised by the academic editor and reviewer(s). You should upload this letter as a separate file labeled 'Response to Reviewers'. A marked-up copy of your manuscript that highlights changes made to the original version. You should upload this as a separate file labeled 'Revised Manuscript with Track Changes'. An unmarked version of your revised paper without tracked changes. You should upload this as a separate file labeled 'Manuscript'. If you would like to make changes to your financial disclosure, please include your updated statement in your cover letter. Guidelines for resubmitting your figure files are available below the reviewer comments at the end of this letter. If applicable, we recommend that you deposit your laboratory protocols in protocols.io to enhance the reproducibility of your results. Protocols.io assigns your protocol its own identifier (DOI) so that it can be cited independently in the future. For instructions see:  http://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols . Additionally, PLOS ONE offers an option for publishing peer-reviewed Lab Protocol articles, which describe protocols hosted on protocols.io. Read more information on sharing protocols at  https://plos.org/protocols?utm_medium=editorial-email&utm_source=authorletters&utm_campaign=protocols . We look forward to receiving your revised manuscript. Kind regards, Jamie Males Staff Editor PLOS ONE Journal Requirements: Please review your reference list to ensure that it is complete and correct. If you have cited papers that have been retracted, please include the rationale for doing so in the manuscript text, or remove these references and replace them with relevant current references. Any changes to the reference list should be mentioned in the rebuttal letter that accompanies your revised manuscript. If you need to cite a retracted article, indicate the article’s retracted status in the References list and also include a citation and full reference for the retraction notice. Additional Editor Comments (if provided): Authors respond to all the comments of both reviewers and editor. All significant points are corrected in the final version and the paper is suitable for being puiblished. Although the novelty of the resultas are scarce, the study is well designed and the methodology have some interest for the region. [Note: HTML markup is below. Please do not edit.] Reviewers' comments: Reviewer's Responses to Questions Comments to the Author 1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation. Reviewer #1: (No Response) Reviewer #2: All comments have been addressed ********** 2. Is the manuscript technically sound, and do the data support the conclusions? The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented. Reviewer #1: Partly Reviewer #2: Yes ********** 3. Has the statistical analysis been performed appropriately and rigorously? Reviewer #1: Yes Reviewer #2: Yes ********** 4. Have the authors made all data underlying the findings in their manuscript fully available? The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified. Reviewer #1: Yes Reviewer #2: No ********** 5. Is the manuscript presented in an intelligible fashion and written in standard English? PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here. Reviewer #1: Yes Reviewer #2: Yes ********** 6. Review Comments to the Author Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters) Reviewer #1: 1. The work is original and will contribute to body of knowledge 2. The author should pay attention and correction the minor edits in the manuscript 3. Figures should carry units 4. Presentation of tables should not be merged together like tables 6-8. Each should be presented separately, highlighting what is significant and relevant to the study. 5. Discussions should focus more on the findings based on the objectives of the study 6. The conclusion should be derived from the outcomes or findings of the study and should not be inferred or extrapolated. Reviewer #2: 1. On page 13, row 229, please clarify the sentence “As the outcome variable is dictums, we applied logistic regression model”. 2. Please indicate in the methods how was central obesity defined. The methods seem to define obesity only and waist circumference, which is not the same as central obesity. The latter is habitually defined as waist to height ratio. 3. There are a couple places in the results where the statement “developed chronic renal failure” is being used. Since this is a cross-sectional study, time-dependent terminology should be avoided. The authors may wish to use something on the line of “had chronic renal failure” instead. 4. The lack of associations with other risk factors than HT might be due to the low prevalence of these other factors, i.e. CVD, diabetes, in the studied population. The authors may wish to comment on this aspect. ********** 7. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files. If you choose “no”, your identity will remain anonymous but your review may still be made public. Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy. Reviewer #1: Yes: Timothy Olusegun Olanrewaju Reviewer #2: No [NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.] While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step. Submitted filename: PONE-D-20-08526_R1_reviewer (1).pdf Click here for additional data file. Submitted filename: The Editor PlosOne.docx Click here for additional data file. 17 Aug 2021 Ref No: PONE-D-20-08526R1 Title: Chronic Kidney Disease and Associated Factors among Adult Population in Southwest Ethiopia Response to reviewers Reviewer #1: 1. The work is original and will contribute to body of knowledge Response: Dear reviewer, thanks for your remark. 2. The author should pay attention and correction the minor edits in the manuscript Response: Dear Reviewer, thanks for your comment and we have corrected the minor edits within the manuscript accordingly. 3. Figures should carry units Response: We have added the units with figures accordingly (Abstract section, page 2, line 26-27, Result section, page 13, line 217, 229 ). 4. Presentation of tables should not be merged together like tables 6-8. Each should be presented separately, highlighting what is significant and relevant to the study. Response: We have cited the tables separately (Result section, page 14, line 251). 5. Discussions should focus more on the findings based on the objectives of the study Response: Dear reviewer, we appreciate your comment. In the discussion section, we tried to be focused based on the two specific objectives of the study. i. the prevalence of CKD based on the GFR estimators and ii. associated factors of CKD. The discussion is based on the finding of the two objectives. 6. The conclusion should be derived from the outcomes or findings of the study and should not be inferred or extrapolated. Response: Dear reviewer, we appreciate your comment and we have corrected the conclusion section mainly on the conclusion on the prevalence of CKD and avoid extrapolation during the conclusion (Conclusions, page 26, line 339). Reviewer #2: 1. On page 13, row 229, please clarify the sentence “As the outcome variable is dictums, we applied logistic regression model”. Response: Thanks for your comment. The sentence “As the outcome variable is dictums, we applied logistic regression model” is to means “As the outcome variable is dichotomous, we applied logistic regression model.” We re-wrote the sentence. It’s to indicate the outcome variable CKD has one of two possible values and fulfills one of the logistic regression assumptions (Result section, page 14, line 232). 2. Please indicate in the methods how was central obesity defined. The methods seem to define obesity only and waist circumference, which is not the same as central obesity. The latter is habitually defined as waist to height ratio. Response: Thanks for your comment and keen observation. The waist circumference is used to assess central obesity and it’s indicated in previous studies [1, 2]. The waist circumference in the current study is used to define central obesity with the cut-point for male ≥102 cm and female ≥88cm. We have corrected the statement accordingly in the definition of variables section of the manuscript (Methods section, Variables’ definition, page 6, line 132-133). 1. Ahmad N, Adam SI, Nawi AM, Hassan MR, Ghazi HF. Abdominal Obesity Indicators: Waist Circumference or Waist-to-hip Ratio in Malaysian Adults Population. Int J Prev Med. 2016 Jun 8;7:82. doi: 10.4103/2008-7802.183654. PMID: 27330688; PMCID: PMC4910307. 2. Lean MEJ, Han TS & Morrison CE (1995): Waist circumference as a measure for indicating the need for weight management. Br. Med. J. 311, 158–161. 3. There are a couple of places in the results where the statement “developed chronic renal failure” is being used. Since this is a cross-sectional study, time-dependent terminology should be avoided. The authors may wish to use something on the line of “had chronic renal failure” instead. Response: We appreciate your comment and have used “had chronic renal failure” rather than “developed chronic renal failure” accordingly (Result section, page 12, 13, line 18,222, 225). 4. The lack of associations with other risk factors than HT might be due to the low prevalence of these other factors, i.e. CVD, diabetes, in the studied population. The authors may wish to comment on this aspect. Response: Dear Reviewer, we appreciate your comment. We strongly believe that the lack of association between CKD and factors such as Diabetes and CVD in the current study might be the low prevalence or the low number of study participants with diabetes and CVD that result from no association during logistic regression analysis. Chronic diseases such as diabetes and CVD are known risk factors indicated in different studies. Submitted filename: Response to Reviewers.docx Click here for additional data file. 9 Feb 2022
PONE-D-20-08526R2
Chronic Kidney Disease and Associated Factors among Adult Population in Southwest Ethiopia
PLOS ONE Dear Dr. Derseh, Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process. The article is much improved after addressing the reviewers comments. However, I think that it needs further improvement and incorporation of relevant literature. In this connection, I suggest to cite the following very relevant articles either in Introduction or Discussion section of the manuscript:
 
https://link.springer.com/article/10.1007/s11845-018-1813-2
https://bmcpublichealth.biomedcentral.com/articles/10.1186/s12889-019-6796-z
https://link.springer.com/article/10.1007/s11255-018-1834-9
https://link.springer.com/article/10.1186/s40545-019-0169-y
https://www.hindawi.com/journals/bmri/2016/9710965/ Please submit your revised manuscript by Mar 26 2022 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at plosone@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file. Please include the following items when submitting your revised manuscript:
If you would like to make changes to your financial disclosure, please include your updated statement in your cover letter. Guidelines for resubmitting your figure files are available below the reviewer comments at the end of this letter. A rebuttal letter that responds to each point raised by the academic editor and reviewer(s). You should upload this letter as a separate file labeled 'Response to Reviewers'. A marked-up copy of your manuscript that highlights changes made to the original version. You should upload this as a separate file labeled 'Revised Manuscript with Track Changes'. An unmarked version of your revised paper without tracked changes. You should upload this as a separate file labeled 'Manuscript'. If applicable, we recommend that you deposit your laboratory protocols in protocols.io to enhance the reproducibility of your results. Protocols.io assigns your protocol its own identifier (DOI) so that it can be cited independently in the future. For instructions see: https://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols. Additionally, PLOS ONE offers an option for publishing peer-reviewed Lab Protocol articles, which describe protocols hosted on protocols.io. Read more information on sharing protocols at https://plos.org/protocols?utm_medium=editorial-email&utm_source=authorletters&utm_campaign=protocols. We look forward to receiving your revised manuscript. Kind regards, Amjad Khan, Ph.D. Academic Editor PLOS ONE Journal Requirements: Please review your reference list to ensure that it is complete and correct. If you have cited papers that have been retracted, please include the rationale for doing so in the manuscript text, or remove these references and replace them with relevant current references. Any changes to the reference list should be mentioned in the rebuttal letter that accompanies your revised manuscript. If you need to cite a retracted article, indicate the article’s retracted status in the References list and also include a citation and full reference for the retraction notice. [Note: HTML markup is below. Please do not edit.] Reviewers' comments: Reviewer's Responses to Questions Comments to the Author 1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation. Reviewer #2: All comments have been addressed ********** 2. Is the manuscript technically sound, and do the data support the conclusions? The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented. Reviewer #2: Yes ********** 3. Has the statistical analysis been performed appropriately and rigorously? Reviewer #2: Yes ********** 4. Have the authors made all data underlying the findings in their manuscript fully available? The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified. Reviewer #2: (No Response) ********** 5. Is the manuscript presented in an intelligible fashion and written in standard English? PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here. Reviewer #2: Yes ********** 6. Review Comments to the Author Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters) Reviewer #2: Kindie Mitiku Kebede et al. studied the burden of CKD and associated risk factors among adults in Southwest Ethiopia for 2018. They found a prevalence of CKD that was comparable with other sub-Saharan African countries, with hypertension and age ≥40 years old being significant risk factors for CKD. The authors have responded satisfactorily to this reviewer's concerns. I have no further comments. ********** 7. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files. If you choose “no”, your identity will remain anonymous but your review may still be made public. Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy. Reviewer #2: No [NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.] While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step.
14 Feb 2022 RESPONSE TO EDITOR AND REVIEWER COMMENTS Dear Editor and Reviewers, The authors sincerely appreciate the time and resources invested in giving such a thorough review. Thank you for the previous comments, suggestions and corrections on the manuscript. We have made efforts to address them and revise the manuscript in line with the comments. The changes have been highlighted in red and tracked in the manuscript. We look forward to a favorable and kind re-consideration. Editor comment The article is much improved after addressing the reviewers comments. However, I think that it needs further improvement and incorporation of relevant literature. In this connection, I suggest to cite the following very relevant articles either in Introduction or Discussion section of the manuscript: https://link.springer.com/article/10.1007/s11845-018-1813-2 https://bmcpublichealth.biomedcentral.com/articles/10.1186/s12889-019-6796-z https://link.springer.com/article/10.1007/s11255-018-1834-9 https://link.springer.com/article/10.1186/s40545-019-0169-y https://www.hindawi.com/journals/bmri/2016/9710965/ Response: Dear Editor, thank you for your insights and the suggested articles to be incorporated within the manuscript. The articles are very interesting. We have added a reference that supports a statement in the discussion section (Ref#30, Page 25, Line 29). However, the other articles are studies on hemodialysis patients (focuses on depression among hemodialysis patients, hypertension control among hemodialysis patients, management of patient care in hemodialysis, and on factors affecting to achieve dry weight in post-dialysis) and we couldn’t cite as our study mainly focuses on the prevalence of CKD through a community-based cross-sectional study. But we will use it for other studies in the future. Submitted filename: Response to Reviewers.docx Click here for additional data file. 15 Feb 2022 Chronic Kidney Disease and Associated Factors among Adult Population in Southwest Ethiopia PONE-D-20-08526R3 Dear Dr. Derseh, We’re pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements. Within one week, you’ll receive an e-mail detailing the required amendments. When these have been addressed, you’ll receive a formal acceptance letter and your manuscript will be scheduled for publication. An invoice for payment will follow shortly after the formal acceptance. To ensure an efficient process, please log into Editorial Manager at http://www.editorialmanager.com/pone/, click the 'Update My Information' link at the top of the page, and double check that your user information is up-to-date. If you have any billing related questions, please contact our Author Billing department directly at authorbilling@plos.org. If your institution or institutions have a press office, please notify them about your upcoming paper to help maximize its impact. If they’ll be preparing press materials, please inform our press team as soon as possible -- no later than 48 hours after receiving the formal acceptance. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information, please contact onepress@plos.org. Kind regards, Amjad Khan, Ph.D. Academic Editor PLOS ONE Additional Editor Comments (optional): Thank you for considering and addressing my comments. Reviewers' comments: 24 Feb 2022 PONE-D-20-08526R3 Chronic Kidney Disease and Associated Factors among Adult Population in Southwest Ethiopia Dear Dr. Abateneh: I'm pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department. If your institution or institutions have a press office, please let them know about your upcoming paper now to help maximize its impact. If they'll be preparing press materials, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information please contact onepress@plos.org. If we can help with anything else, please email us at plosone@plos.org. Thank you for submitting your work to PLOS ONE and supporting open access. Kind regards, PLOS ONE Editorial Office Staff on behalf of Dr. Amjad Khan Academic Editor PLOS ONE
  30 in total

Review 1.  Chronic kidney disease among human immunodeficiency virus positive patients on antiretroviral therapy in sub-Saharan Africa: A systematic review and meta-analysis.

Authors:  Habtamu Wondifraw Baynes; Markos Negash; Demeke Geremew; Zegeye Getaneh
Journal:  Saudi J Kidney Dis Transpl       Date:  2019 Nov-Dec

2.  Salt and blood pressure in various populations.

Authors:  N Poulter; K T Khaw; B E Hopwood; M Mugambi; W S Peart; P S Sever
Journal:  J Cardiovasc Pharmacol       Date:  1984       Impact factor: 3.105

Review 3.  Epidemiology, impact and preventive care of chronic kidney disease in Taiwan.

Authors:  Shang-Jyh Hwang; Jer-Chia Tsai; Hung-Chun Chen
Journal:  Nephrology (Carlton)       Date:  2010-06       Impact factor: 2.506

4.  Screening for CKD with eGFR: doubts and dangers.

Authors:  Richard J Glassock; Christopher Winearls
Journal:  Clin J Am Soc Nephrol       Date:  2008-07-30       Impact factor: 8.237

5.  Risk of developing low glomerular filtration rate or elevated serum creatinine in a screened cohort in Okinawa, Japan.

Authors:  Kunitoshi Iseki; Chiho Iseki; Yoshiharu Ikemiya; Kozen Kinjo; Shuichi Takishita
Journal:  Hypertens Res       Date:  2007-02       Impact factor: 3.872

6.  Prevalence of chronic kidney disease in Kinshasa: results of a pilot study from the Democratic Republic of Congo.

Authors:  Ernest K Sumaili; Jean-Marie Krzesinski; Chantal V Zinga; Eric P Cohen; Pierre Delanaye; Sylvain M Munyanga; Nazaire M Nseka
Journal:  Nephrol Dial Transplant       Date:  2008-08-20       Impact factor: 5.992

7.  Prevalence and risk factors of chronic kidney disease in urban adult Cameroonians according to three common estimators of the glomerular filtration rate: a cross-sectional study.

Authors:  Francois Folefack Kaze; Marie-Patrice Halle; Hermine Tchuendem Mopa; Gloria Ashuntantang; Hermine Fouda; Jeanne Ngogang; Andre-Pascal Kengne
Journal:  BMC Nephrol       Date:  2015-07-07       Impact factor: 2.388

8.  Chronic kidney disease and underdiagnosis of renal insufficiency among diabetic patients attending a hospital in Southern Ethiopia.

Authors:  Temesgen Fiseha; Mehidi Kassim; Tilahun Yemane
Journal:  BMC Nephrol       Date:  2014-12-15       Impact factor: 2.388

Review 9.  Global Prevalence of Chronic Kidney Disease - A Systematic Review and Meta-Analysis.

Authors:  Nathan R Hill; Samuel T Fatoba; Jason L Oke; Jennifer A Hirst; Christopher A O'Callaghan; Daniel S Lasserson; F D Richard Hobbs
Journal:  PLoS One       Date:  2016-07-06       Impact factor: 3.240

10.  Renal Function Impairment and Associated Factors among HAART Naïve and Experienced Adult HIV Positive Individuals in Southwest Ethiopia: A Comparative Cross Sectional Study.

Authors:  Yewulsew Mekuria; Daniel Yilma; Zeleke Mekonnen; Tesfaye Kassa; Lealem Gedefaw
Journal:  PLoS One       Date:  2016-08-18       Impact factor: 3.240

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