Literature DB >> 27171139

Prevalence and Predictors of Iron Deficiency Anemia in Children under Five Years of Age in Pakistan, A Secondary Analysis of National Nutrition Survey Data 2011-2012.

Muhammad Atif Habib1,2, Kirsten Black1, Sajid Bashir Soofi2, Imtiaz Hussain2, Zaid Bhatti2, Zulfiqar A Bhutta2, Camille Raynes-Greenow3.   

Abstract

BACKGROUND: Iron deficiency Anemia (IDA) in children is a recognized public health problem that impacts adversely on child morbidity, mortality and impairs cognitive development. In Pakistan information on the true prevalence and predictors of IDA is limited. This study sought to investigate IDA in children under five years of age using data from a nationally representative stratified cross-sectional survey.
METHODS: Secondary analysis was performed on the National Nutrition Survey in Pakistan 2011-2012. We used a pre-structured instrument to collect socio demographic and nutritional data on mothers and children. We also collected Anthropometric measurements and blood samples for micronutrient deficiencies. IDA was defined as having both haemoglobin levels of <110 g/L and ferritin levels of < 12 μg/L. Data analysis was performed by applying univariate and multivariate techniques using logistic regression through SPSS.
FINDINGS: A total of 7138 children aged between 6-59 months were included in the analysis. The prevalence of IDA was 33.2%. In multivariate regression analysis adjusted odds ratios (AOR) were calculated. Age < 24 months (AOR 1.40, 95% CI 1.18-1.55 p <0.05), stunting (AOR 1.42 CI 1.23-1.63 p<0.05), presence of clinical anemia (AOR 5.69 CI 4.93-6.56 p<0.05), having a mother with IDA (AOR 1.72 CI 1.47-2.01 p<0.05) and household food insecurity (AOR 1.20 CI 1.10-1.40 P<0.05) were associated with IDA. Living in a rural area (AOR 0.77 CI 0.65-0.90 p<0.05) and being a female child (AOR 0.87 CI 0.76-0.98 p<0.05) were associated with reduced odds of IDA.
CONCLUSION: The prevalence of IDA amongst Pakistani children represents a moderate burden that disproportionately affects the youngest, growth retarded children, affected children are more likely to have mothers with IDA and live in areas where food security is lacking. National efforts to alleviate the burden of IDA should involve both short term vertical programs such as iron supplementation and long term horizontal programs including wheat flour fortification.

Entities:  

Mesh:

Year:  2016        PMID: 27171139      PMCID: PMC4865153          DOI: 10.1371/journal.pone.0155051

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


Introduction

Iron deficiency anemia in young children is recognized as a major public health issue and the most prevalent form of micronutrient deficiency worldwide [1, 2]. The global prevalence of anemia (defined as hemoglobin level of <110 g/L) in children aged 6–59 months is 43% and half is attributable to iron deficiency anemia (IDA) which is defined as hemoglobin level of <110g/L and ferritin level of < 12 μg/L [1-4]. IDA contributes substantially to childhood mortality and morbidity and is linked to impaired brain development and cognitive functions [5-9]. IDA is also ranked as the third leading cause of disability worldwide and the 13th leading risk factor for the global disability adjusted life years [10]. Most of the burden of IDA is in the resource poor settings of Africa and Asia [4, 11]. In Pakistan the reported prevalence of IDA in children under five is between 40–70% [12-16]. In Pakistani children IDA has been associated with growth retardation, impaired cognition, reduced physical activity and postulated as a contributor to the high national infant mortality rate [10, 12, 14, 17, 18, 19]. Widespread micronutrient deficiencies along with other clinical and social factors are believed to be the leading cause of IDA in Pakistan [13-18]. However prevalence data is scarce with many studies more than a decade old, or based on small numbers and in small non-representative populations. Further, IDA is best defined as the combination of both low hemoglobin and low ferritin concentrations, whereas the published studies to date from Pakistan are mostly based solely on hemoglobin concentrations. As such, nationally representative robust data are still lacking to determine the socio-demographic factors associated with IDA that will enable the development of local strategies to treat and prevent IDA in Pakistani children. In this study we aimed to estimate the prevalence of IDA in Pakistani children and to evaluate factors associated with IDA by conducting a secondary analysis of the Pakistan National Nutrition Survey that was undertaken between 2011–2012.

Materials and Methods

Data source

The data used for this analysis were derived from the Pakistan National Nutrition Survey 2011–2012. The survey was conducted by the Aga Khan University (AKU) in collaboration with the Federal Ministry of Health in Pakistan and was funded by UNICEF. The survey was a stratified representative cross-sectional national survey with provincial specificity, with a two-stage stratified sampling design. The sampling frame in the form of Enumeration blocks (1500 in number) was provided by the Pakistan Federal Bureau of Statistics. Each enumeration block was demarcated, mapped and listed before the actual data collection and from each enumeration block 20 households were selected randomly through a computer generated program. A total of 30,000 households were included, 12,360 were urban households and 17,640 were rural, resulting in 27,963 respondents. Households with children between the ages of six months to five years were included in the survey. One married woman of reproductive age (15–49 years) with at least one child aged less than 5 years was chosen from each selected household. If there were multiple eligible women in a household, one woman was randomly selected. A pre structured and pre tested instrument was used for data collection. The instrument collected data on socio-economic status, maternal reproductive history, child medical history, food security, anthropometric measurements and biochemical measurements of various micronutrients. For anthropometric measurements weight was measured using lightweight SECA scales designed and manufactured under the authority of the United Nations Children’s Fund (UNICEF) and the height/lengths was measured by height boards made by Shorr Inc. Children under 2 years of age were measured lying down on the board and standing height was measured for older children [20]. In children more than 2 years height-for-age z scores (HAZ), weight-for-age z scores (WAZ), weight-for-height z scores (WHZ) were calculated and for children less than 2 years length was used instead of height to calculate length-for-age z scores (LAZ) and weight-for-length z scores (WLZ). Body Mass Index (BMI) was calculated for mothers using height and weight. Children were reported as stunted, wasted or undernourished and mothers were reported as underweight, overweight or obese as per the WHO classification [21]. Blood samples for hemoglobin measurement and micronutrient deficiencies were collected from one child in each household. Venous blood was collected and serum was separated within half hour of collection, using portable centrifuge machines with backup power. The hemoglobin was measured from the venous blood at field while the serum samples were transported to nutrition research laboratory at Aga Khan University under cold chain conditions through country wide network of AKU laboratories collection centres. Serum Ferritin concentrations were measured for iron deficiency because it has the highest sensitivity and specificity to detect iron deficiency in individuals [22]. The ferritin levels were adjusted for alpha (1)-acid glycoprotein (AGP) and C-reactive protein (CRP) to take into account that ferritin is an acute phase protein and is raised in inflammatory conditions [23-24]. Serum Ferritin was measured by electro-chemiluminescence immunoassay using Roche Cobas E41 Chemistry Analyzer and hemoglobin concentration was measured in whole blood using a Micro cuvette containing a dry reagent system and a dual wavelength HemoCue 201 Photometer. Hemoglobin concentration was also adjusted for altitudes of more than 1000 meters using the WHO recommended altitude formula [25]. Blood samples were also analyzed for zinc deficiency and vitamin A deficiency. Serum was used to estimate the zinc and vitamin A deficiency and the samples were analyzed using Spectrophotometric method for zinc deficiency and Reversed Phase Chromatography method for vitamin A deficiency. All survey activities were monitored to ensure the data quality. The questionnaire was pre-tested prior to implementation in the field and a pilot survey was also conducted. Competency of field staff was also taken in account prior to hiring and pre-test and post-test was conducted for all field staff during trainings. The survey employed internal and external data monitors to ensure data quality with respect to the all the procedures and survey activities. The anthropometry and equipment HemoCue was calibrated daily for any possible errors. The team leaders analyzed the data (plausibility checks and digit preference) using ENA Smart software and provided regular feedback for improvement. Similar quality assurance steps were duly considered during data entry and cleaning. Ethical approval for the survey was obtained from the Ethical Review Committee of Aga Khan University and the National Bioethics committee of Pakistan. Written informed consent was obtained from the mothers of the selected child. In case of illiterate mother, consent was documented by a thumbprint on the consent form and a signature by a literate witness. All the names and personal information regarding the participants were kept confidential and data set was kept anonymous for analysis.

Description of Variables

Child IDA status was the main outcome variable and was defined as the having the combination of haemoglobin levels of <110 g/L and ferritin levels of < 12 μg/L [26]. The selection of explanatory variables for analysis was informed by the literature and their availability in the dataset and is fully described in Table 1. Variables were grouped into three categories; household, maternal, and child. Under the household category area of residence which was categorized into rural and urban, socioeconomic status which was ascertained by computing the wealth quintiles (from being poorest to wealthiest) using the standard demographic and health survey tool and food security status using the standard household food insecurity access scale developed by Food and Nutrition Technical Assistance (FANTA) project [27] and categorized as (Food Secure and Food insecure) were considered. In the maternal category maternal education which was defined as years of education completed (illiterate/years of education), maternal IDA estimated on the basis of low hemoglobin (< 120 g/L) and low ferritin (< 12 μg/L) concentrations and maternal BMI calculated on the basis of height and weight of mother and categorized as <18.5 underweight, 18.5–24.99 normal weight, 25–34.99 overweight/obesity and ≥35 severe obesity, were examined. In the child variables sex, age, clinical anemia estimated through physical examination of conjunctiva, vitamin A deficiency defined as serum vitamin A concentration of < = 0.70 μmol/L and categorized as deficient and non-deficient, zinc deficiency defined as serum zinc concentration of <60 μg/dL and categorized as deficient and non-deficient, stunting defined as height/length-for-age z-score of < −2, wasting defined as weight for height z-score of < −2, underweight defined as weight for age z-score of < −2 as per and history of worm infestation ascertained through recall of worm infestation in last six months.
Table 1

Description of Explanatory Variables used in the Analysis.

VariablesDescription
Household level factors
Area of residenceurban and rural
Socio economic status of the householdSES was measured as quintiles of a linear index derived from household assets and utilities score, the wealth quintiles were divided into five (poorest, poorer, middle, richer, richest)
Food security statusFood security status was measured by using the standard household food and hunger scale developed by Food and Nutrition Technical Assistance (FANTA) project and categorized as (Food Secure and Food insecure)
Maternal Factors
Maternal EducationYears of education completed (illiterate/years of education)
Maternal Iron deficiency anemia statusHemoglobin levels of <120 g/L and serum ferritin levels of <12 μg/L. Categorized as Iron deficiency anemic and normal
Maternal BMICalculated on the basis of height and weight of mother and categorized as <18.5 underweight, 18.5–24.99 normal weight, 25–34.99 overweight/obesity and ≥35 severe obesity.
Children factors
SexMale, female
AgeCategorized as <24 months, 24–59 months
AnemiaHemoglobin concentration of <110 g/L in whole blood and characterized as anemia
Clinical AnemiaPresence of anemia on physical examination i-e conjunctival and palmar pallor and categorized as Yes or No
Vitamin A DeficiencySerum vitamin A concentration of < = 0.70 μmol/L and categorized as deficient and non-deficient
Zinc DeficiencySerum zinc concentration of <60 μg/dL and categorized as deficiency
Height for Age–StuntedHeight/length-for-age z-score of < −2 as per WHO standards and categorized as stunted
Weight for Height—WastedWeight for height z-score of < −2 as per WHO standards and categorized as wasted
Weight for Age—Under weightWeight for age z-score of < −2 as per WHO standards and categorized as underweight
History of worm infestationHistory of worm infestation in the previous six months and categorized as Yes or No

Statistical Analysis:

All data analyses were conducted in IBM SPSS version 19 [28] using a complex sample procedure to allow for adjustments of the sampling design implemented in the survey. The frequencies, along with weighted percentages, were reported for selected predictors and the mean with 95% confidence intervals (CIs) were calculated for the outcomes. The analysis started with simple univariate analysis followed by multivariate logistic regression. Unadjusted odds ratio with their 95% CIs were reported for the bivariate analysis. Variables significant at p<0.25 were considered for inclusion in the multivariate model. Covariates that were insignificant at the multivariate level were dropped consecutively from the model after careful assessment of confounding. The final model was selected on the basis of theoretical and statistical significance of predictors. The Type 1 error rate was set at 0.05. The model estimates are presented with the adjusted odds ratios and 95% CI.

Results

A total of 7138 children aged between 6–59 months were included in the analysis among them 2373 (33.2%) children had IDA based on low hemoglobin and ferritin levels. Analyses of the child blood samples found that overall (4264) 62.3% were anemic (hemoglobin concentrations <110 g/L), of those who were anemic (283) 4.1% were severely anemic (< 70 g/L) and (3981) 58.3% were moderately anemic (70 g/L – 109 g/L). Ferritin deficiency was identified in (3361) 47.1% children. Among those who had IDA the mean values for hemoglobin and ferritin concentrations were 70 g/L and 6μg/L respectively. The prevalence for vitamin A deficiency and zinc deficiency was 52.6% and 38.8% respectively. Clinical anemia was found in 30.1% children. The anthropometric data identified 44.5% of the children as being stunted, 15.5% as wasted and 33.6% as underweight. Among maternal factors the prevalence of IDA was found to be 20.0%, which was determined by using maternal hemoglobin and ferritin levels, and according to the maternal anthropometrics 16.0% of mothers were classified as underweight, 21.2% overweight and 11.1% obese. Among all children included in the analysis the majority of children came from rural areas (70.1%), 48.3% of children were female and 47.9% were under the age of 24 months. The two lowest wealth quintiles accounted for 43.3% of the study population, and the two highest was 36.0%. Of the sampled households 64.3%were food insecure. Only 8.3% of the mothers reported that their child had worm infestation in last six months (Table 2).
Table 2

Background characteristics of sampled children (6–59 months) in National Nutrition Survey Pakistan (N = 7138).

Background characteristicsN(%)95% CI
Residence
  Rural433170.366.6–73.2
  Urban280729.726.8–33.4
Wealth quintiles
Poorest153323.020.4–25.3
2139020.318.35–22.0
3150020.819.1–22.6
4145219.418.1–21.7
5 wealthiest126316.614.3–18.4
Food security
    Food insecure433964.362.2–66.6
    Food secure261535.733.4–37.8
Maternal Education
  Illiterate401558.054.8–60.1
  Primary or less (1–5 years of completed schooling)101814.713.6–16.7
  Middle(6–8)6058.37.3–9.7
  Matric(9–10)81510.89.6–12.3
  Intermediate & above (>10)6408.36.7–9.5
Maternal iron deficiency anemia Status
  Anemic121220.019.8–23.4
  Normal512780.076.6–80.3
Maternal BMI (kg/m2)
  <18.5 (Underweight)111716.014.9–17.8
  18.5–24.9 (Normal)366051.749.7–63.8
  25–29.9 (Overweight)154321.219.3–22.7
  > = 30 (Obese)81811.19.6–12.1
Sex
  Female343948.345.8–49.8
  Male369951.750.3–54.2
Age in months
    24-59m375552.147.2–51.3
    <24m338347.948.7–52.8
Presence of clinical Anemia
    Yes205730.133.1–37.7
    No502269.962.4–66.9
Hemoglobin Levels
  Anemic (Hb < 110 g/l)426462.358.2–65.5
  Severely anemic (Hb < 70g/l)2834.13.4–5.9
  Moderately anemic (HB 70–109 g/l)398158.355.4–60.1
  Normal (Hb > 110m/l)280837.735.8–40.2
Ferritin Levels
  Ferritin deficient (<12 μg/l)336147.130.7–35.4
  Ferritin Normal (>12 μg/l)377752.962.6–69.2
Vitamin A Levels
    Deficient (< = 0.70 μmol/l)369452.649.6–55.1
    Non deficient (>0.70 μmol/l)319847.444.9–50.4
Zinc Levels
    Deficient (<60 μg/dl)262538.836.2–41.1
    Non-Deficient (60–150 μg/dl)416661.258.9–63.7
Height for Age–Stunted
    Stunting (-6 to -2)306144.543.7–48.1
    Normal (-1.99 to +6)386255.551.9–56.3
Weight for Height—Wasted
    Wasting (-5 to -2)105015.514.1–16.8
    Normal (-1.99 to +5)580984.583.2–86.0
Weight for Age—Under weight
    Underweight (-6 to -2)231533.632.6–36.5
    Normal (-1.99 to +5)470566.463.5–67.5
History of worm infestation
Yes5978.37.5–9.9
No636991.790.1–92.5
The univariate analysis (Table 3) showed that the IDA in children under five years of age in Pakistan was significantly associated with: age of less than 24 months (OR 1.45 1.29–1.62 p <0.05), stunting (OR 1.44 1.27–1.64 p<0.05), being underweight (OR 1.28 1.15–1.43 p<0.05), presence of clinical anemia (OR 5.03 4.41–5.74 p<0.05), history of worm infestation (OR 1.33 1.10–1.62 p<0.05), having a mother with IDA (OR 1.91 1.65–2.21 p<0.05) and household food insecurity (OR 1.23 1.08–1.41 p<0.05).
Table 3

Factors associated with Iron deficiency anemia among children 6–59 months of age in Pakistan, Univariate and Multivariate analysis (N = 2373).

CharacteristicsIDA(95% CI)Un adjusted OR (95% CI)P-valueAdjusted OR (95% CI)P-value
Household factors
Residence
  Rural1423 (68.8)65.2–72.30.89 (0.79–1.02)0.0880.77 (0.65–0.90)0.001
  Urban950 (31.2)27.7–34.8Ref.
Wealth quintiles
  Poorest505 (22.3)19.8–24.81.04 (0.86–1.26)0.6550.65 (0.51–0.85)
  2448 (19.9)17.9–21.91.06 (0.88–1.29)0.5450.83 (0.65–1.05)
  3509 (20.9)19.0–22.31.11 (0.91–1.35)0.3140.99 (0.79–1.26)
  4510 (21.2)19.2–23.31.26 (1.04–1.51)0.0171.19 (0.96–1.48)
  5 wealthiest401 (15.6)13.4–17.8Ref.Ref.
Food security
  Food insecure1460 (64.7)62.2–67.11.23 (1.08–1.41)0.0031.20 (1.10–1.40)0.002
  Food secure860 (35.3)32.9–37.8Ref.
Maternal factors
Maternal Education
  Illiterate1293 (55.6)52.7–58.41.11 (0.86–1.41)0.439
  Primary or less (1–5)378 (16.4)14.6–18.31.41 (1.07–1.85)0.016
  Middle(6–8)218 (9.3)7.8–10.71.40 (1.03–1.9)0.032
  Matric(9–10)288 (11.4)9.8–12.91.28 (0.96–1.7)0.09
  Intermediate & above (>10)183 (7.4)5.8–9.0Ref.
Maternal iron deficiency anema
  Anemic558 (26.9)24.6–29.31.91 (1.65–2.21)0.0001.72 (1.47–2.01)0.001
  Normal1577 (73.1)70.7–75.4Ref.Ref.
BMI (kg/m2)
  <18.5410 (17.5)15.8–19.11.12 (0.97–1.29)0.130
  18.5–24.91223 (52.5)50.2–54.7Ref.
  25–29.9493 (20.1)18.2–22.10.92 (0.79–1.04)0.163
  > = 30247 (9.9)8.6–11.30.83 (0.69–0.99)0.042
Child’s factors
Child’s sex
  Female1067 (45.9)43.5–48.40.86 (0.77–0.97)0.0120.87 (0.76–0.98)0.028
  Male1306 (54.1)51.6–56.5Ref.Ref.
Child’s Age in months
  <24m1252 (53.9)51.5–56.21.45 (1.29–1.62)0.0001.35 (1.18–1.55)0.0002
  24-59m1121 (46.1)43.8–48.5Ref.Ref.
Presence of clinical Anemia in children
  Yes1229 (52.6)49.7–55.65.03 (4.41–5.74)0.0005.69 (4.93–6.56)0.0001
No1131 (47.4)44.4–50.3Ref.Ref.
Vitamin A deficiency
  Deficient (< = 0.70 μmol/l)1221 (51.5)48.5–54.50.93 (0.83–1.05)0.261
  Non deficient (>0.70 μmol/l)1084 (48.5)45.5–51.5Ref.
Zinc deficiency
  Deficient (<60 μg/dl)852 (37.8)34.9–40.61.07 (0.95–1.21)0.240
  Non-Deficient (60–150 μg/dl)1409 (62.2)59.4–65.1Ref.
Height for Age–Stunted
  Stunting(-6 to -2)1158 (50.4)47.9–52.91.44 (1.27–1.64)0.0001.42 (1.23–1.63)0.0001
  Normal(-1.99 to +6)1160 (49.6)47.1–52.2Ref.Ref.
Weight for Height–Wasted
  Wasting(-5 to -2)351 (15.1)13.5–16.70.95 (0.82–1.11)0.532
  Normal(-1.99 to +5)1963 (84.9)83.3–86.5Ref.
Weight for Age—Under weight
  Underweight(-6 to -2)868 (37.3)35.0–39.61.28 (1.15–1.43)0.000
  Normal(-1.99 to +5)1481 (62.7)60.4–65.0Ref.
History of worm infestation
  Yes218 (9.8)8.4–11.31.33 (1.1–1.62)0.003
  No2093 (90.2)88.7–91.6Ref.
In the multivariate regression (Table 3) only being underweight was no longer a significantly increased risk with childhood IDA and of the variables that remained the adjusted odds ratios were slightly attenuated: age < 24 months (AOR 1.40, 95% CI 1.18–1.55 p <0.05), stunting (AOR 1.42 CI 1.23–1.63 p<0.05), having a mother with IDA (AOR 1.72 CI 1.47–2.01 p<0.05) and household food insecurity (AOR 1.20 CI 1.10–1.40 P<0.05), except for presence of clinical anemia for which the adjusted OR increased (AOR 5.69 CI 4.93–6.56 p<0.05). In contrast, living in a rural area (AOR 0.77 CI 0.65–0.90 p<0.05) and being a female child (AOR 0.87 CI 0.76–0.98 p<0.05) was associated with reduced odds of IDA (Table 3).

Discussion

In our study, the prevalence of IDA in children aged 6–59 months was 33.2% which according to the WHO criteria represents a ‘moderate burden’ [2]. We also found a substantial prevalence of low hemoglobin levels, vitamin A deficiency, zinc deficiency, stunting, wasting, underweight and food insecurity amongst children aged 6–59 months living in Pakistan. The prevalence of IDA in our study is lower than in previous studies in other low resource countries such as Palestine and Kenya [29-30] and substantially below the estimate from a previous study in Pakistan [14]. These differences could be attributed to variations in the study settings or factors such as the rate of parasitic infections and dietary habits. The previously published study from Pakistan, reported a prevalence of IDA of 63% from a smaller sample (n = 320) taken from a semi urban area, which is not comparable with this population based survey. Additionally it was conducted 18 years ago, before the introduction of the iron fortification in Pakistan [31]. Our findings are consistent with IDA prevalence reported in Kazakhstan (32.4%) [32], Yemen (34.2%) [33] and the Pakistan National Nutrition Survey (36%) undertaken in 2001 [13] but are higher than studies conducted in Morocco (20.4%) [34], India (23.1%) [35] and Iran (29.1%) [36]. Our study found that the food insecurity status of households is significantly associated with IDA in children, a finding that is consistent with the available literature examining this association [37, 38, and 39]. Food insecurity is characterized by either unavailability of food or inability to procure and access food and has consequences in both macro and micronutrient deficiencies. In Pakistan the widespread food insecurity situation reflects the economic instability of many areas of the country [40]. The study found a relationship between maternal iron deficiency anemia and IDA in children that confirms previous reports [18, 41–43] and highlights that IDA is common in pregnant and non-pregnant women of reproductive age in Pakistan [13]. In our study clinical examination of children detected clinical anemia in 53.6% of IDA cases. This sign can therefore assist in diagnosis where facilities for biochemical testing are not available. We found the prevalence of IDA to be significantly associated with children’s age, with the youngest children having the highest odds of IDA. This finding is consistent with similar studies conducted in Iran, India and the Philippines [36, 39, 44]. The first two years of life is a period of rapid growth with an increased iron requirement therefore risk of IDA is increased in this age. Moreover factors such as limited access to iron rich food, inadequate infant and young child feeding practices including lack of exclusive breast feeding, prolonged breast feeding and inappropriate weaning food and recurrent illnesses increase the chance of young children developing IDA [17, 39, and 45]. We also found that the odds of IDA increased when the child was stunted and food insecure, suggesting that malnutrition is a contributing factor for IDA [9, 13, 46]. After adjusting for other factors, our study found that female children and those residing in rural areas were less likely to develop IDA. There is conflicting evidence with regard to the relationship between sex and IDA in children. Contrary to our study, data from Yemen and India found a higher prevalence of IDA in girls than boys [36, 47]; however studies from Western Kenya and Haiti found boys to be more at risk [48, 49]. In our setting children living in rural areas have more access to green leafy vegetables which may explain their reduced risk of IDA. The major strength of this study is the nationally representative sample using reliable methods to detect iron and adjustment for confounding factors. However this study also has some limitations. The cross-sectional nature of the study means that the temporal relationship between IDA and the associated factors cannot be established. The information on various indicators was collected using a structured questionnaire that may have been prone to recall bias and presence of some missing data is also a potential limitation. Moreover we did not measure serum vitamin B12 and folate levels and so cannot measure other forms of anemia, suggesting some misclassification bias. The data presented provides valuable insight into the prevalence of IDA in children which has remained fairly consistent in Pakistan over the last decade. Considering the burden of IDA in Pakistani children it is essential that interventions such as iron supplementation, food fortification and diet diversification should be used at scale [50], currently iron supplementation and wheat flour fortification are successful strategies being used worldwide. There is good evidence to suggest that iron supplementation improves hemoglobin level and reduces IDA prevalence in children [51-53]. Studies conducted in Pakistan also reveal iron supplementation to children and mothers results in improved iron stores [54-56]. Further a recent pooled analysis and studies in Central Asia, Venezuela and Iran suggest that wheat flour fortification can significantly improve iron status at the population level [54, 57–60] but there is a lack of such supplementation programs in Pakistan. To reduce the burden of IDA, Pakistan needs a holistic approach of short term vertical programs such as iron supplementation and long term horizontal programs including wheat flour fortification. Specifically, further efforts should be made to restore the national wheat flour fortification program as wheat is the staple diet of Pakistan. Additional investments are also required to improve; education, especially for females, food insecurity through food supplements and agricultural support. These may require novel methods such as behavioral change communications to improve dietary patterns and infant and young child complementary feeding (IYCF) practices. Finally for this generation of Pakistani children to benefit it is important that Pakistan acts swiftly to alleviate the prevalence of IDA.
  39 in total

Review 1.  Diagnosis and management of iron deficiency anaemia: a clinical update.

Authors:  Sant-Rayn S Pasricha; Stephen C Flecknoe-Brown; Katrina J Allen; Peter R Gibson; Lawrence P McMahon; John K Olynyk; Simon D Roger; Helen F Savoia; Ramdas Tampi; Amanda R Thomson; Erica M Wood; Kathryn L Robinson
Journal:  Med J Aust       Date:  2010-11-01       Impact factor: 7.738

2.  Anaemia in low-income and middle-income countries.

Authors:  Yarlini Balarajan; Usha Ramakrishnan; Emre Ozaltin; Anuraj H Shankar; S V Subramanian
Journal:  Lancet       Date:  2011-08-01       Impact factor: 79.321

3.  A comparative evaluation of multiple micronutrient and iron-folic acid supplementation during pregnancy in Pakistan: impact on pregnancy outcomes.

Authors:  Zulfiqar A Bhutta; Arjumand Rizvi; Farrukh Raza; Sunil Hotwani; Shujaat Zaidi; S Moazzam Hossain; Sajid Soofi; Shereen Bhutta
Journal:  Food Nutr Bull       Date:  2009-12       Impact factor: 2.069

4.  Fetal iron status in maternal anemia.

Authors:  P N Singla; M Tyagi; R Shankar; D Dash; A Kumar
Journal:  Acta Paediatr       Date:  1996-11       Impact factor: 2.299

Review 5.  A question mark on iron deficiency in 185 million people of Pakistan: its outcomes and prevention.

Authors:  Anwaar Ahmed; Asif Ahmad; Nauman Khalid; Angel David; Mansoor Abdullah Sandhu; Muhammad Atif Randhawa; Hafiz Ansar Rasul Suleria
Journal:  Crit Rev Food Sci Nutr       Date:  2014       Impact factor: 11.176

6.  Iron depletion and anaemia: prevalence, consequences, diagnostic and therapeutic implications in a developing Pakistani population.

Authors:  P Hamedani; K Z Hashmi; M Manji
Journal:  Curr Med Res Opin       Date:  1987       Impact factor: 2.580

7.  Anemia and iron deficiency among schoolchildren in the Aral Sea region, Kazakhstan.

Authors:  M Hashizume; O Kunii; S Sasaki; T Shimoda; S Wakai; Z Mazhitova; D Dauletbaev; W Caypil; M Aldiyarova; A Farmer; Y Yamashiro; M Chiba
Journal:  J Trop Pediatr       Date:  2003-06       Impact factor: 1.165

8.  Iron-deficiency anemia among children in southwest Iran.

Authors:  Bijan Keikhaei; Khodamorad Zandian; Ali Ghasemi; Ramin Tabibi
Journal:  Food Nutr Bull       Date:  2007-12       Impact factor: 2.069

9.  Anaemia control: lessons from the flour fortification programme.

Authors:  J Sadighi; K Mohammad; R Sheikholeslam; M A Amirkhani; P Torabi; F Salehi; Z Abdolahi
Journal:  Public Health       Date:  2009-11-14       Impact factor: 2.427

10.  Determinants of anemia among preschool children in rural, western Kenya.

Authors:  Eric M Foote; Kevin M Sullivan; Laird J Ruth; Jared Oremo; Ibrahim Sadumah; Thomas N Williams; Parminder S Suchdev
Journal:  Am J Trop Med Hyg       Date:  2013-02-04       Impact factor: 2.345

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  15 in total

Review 1.  Prevalence and Associated Factors of Iron Deficiency and Iron Deficiency Anemia Among Under-5 Children: A Systematic Review and Meta-Analysis.

Authors:  Solomon Gedfie; Solomon Getawa; Mulugeta Melku
Journal:  Glob Pediatr Health       Date:  2022-07-06

2.  Age, Ethnicity, Glucose-6-Phosphate Dehydrogenase Deficiency, Micronutrient Powder Intake, and Biomarkers of Micronutrient Status, Infection, and Inflammation Are Associated with Anemia Among Children 6-59 Months in Nepal.

Authors:  Nicole D Ford; R P Bichha; Kedar Raj Parajuli; Naveen Paudyal; Nira Joshi; Ralph D Whitehead; Stanley Chitekwe; Zuguo Mei; Rafael Flores-Ayala; Debendra P Adhikari; Sanjay Rijal; Maria Elena Jefferds
Journal:  J Nutr       Date:  2020-04-01       Impact factor: 4.798

3.  Complementary Feeding of Sorghum-Based and Corn-Based Fortified Blended Foods Results in Similar Iron, Vitamin A, and Anthropometric Outcomes in the MFFAPP Tanzania Efficacy Study.

Authors:  Nicole M Delimont; Christopher I Vahl; Rosemary Kayanda; Wences Msuya; Michael Mulford; Paul Alberghine; George Praygod; Julius Mngara; Sajid Alavi; Brian L Lindshield
Journal:  Curr Dev Nutr       Date:  2019-04-10

4.  Correlation between maternal and childhood VitB12, folic acid and ferritin levels.

Authors:  Fatima Zeeshan; Attia Bari; Saima Farhan; Uzma Jabeen; Ahsan Waheed Rathore
Journal:  Pak J Med Sci       Date:  2017 Jan-Feb       Impact factor: 1.088

5.  Ferritin Is a Marker of Inflammation rather than Iron Deficiency in Overweight and Obese People.

Authors:  Abidullah Khan; Wazir Muhammad Khan; Maimoona Ayub; Mohammad Humayun; Mohammad Haroon
Journal:  J Obes       Date:  2016-12-27

6.  Frequency of Anemia and Iron Deficiency among Children Starting First Year of School Life and Their Association with Weight and Height.

Authors:  Mirza Sultan Ahmad; Hadia Farooq; Sumaira Noor Maham; Zonaira Qayyum; Abdul Waheed; Waqar Nasir
Journal:  Anemia       Date:  2018-04-10

7.  Factors influencing childhood anaemia in Bangladesh: a two level logistic regression analysis.

Authors:  Abu Yusuf; A S M A Mamun; Md Kamruzzaman; Aik Saw; Nagah M Abo El-Fetoh; Pete E Lestrel; Md Golam Hossain
Journal:  BMC Pediatr       Date:  2019-06-29       Impact factor: 2.125

8.  Micronutrient Deficiencies and Stunting Were Associated with Socioeconomic Status in Indonesian Children Aged 6-59 Months.

Authors:  Fitrah Ernawati; Ahmad Syauqy; Aya Yuriestia Arifin; Moesijanti Y E Soekatri; Sandjaja Sandjaja
Journal:  Nutrients       Date:  2021-05-26       Impact factor: 5.717

9.  Iron deficiency anemia among children aged 2-5 years in southern Ethiopia: a community-based cross-sectional study.

Authors:  Alemselam Zebdewos Orsango; Wossene Habtu; Tadesse Lejisa; Eskindir Loha; Bernt Lindtjørn; Ingunn Marie S Engebretsen
Journal:  PeerJ       Date:  2021-06-28       Impact factor: 2.984

10.  Dietary Balance Index-07 and the Risk of Anemia in Middle Aged and Elderly People in Southwest China: A Cross Sectional Study.

Authors:  Qiang Zhang; Guanghe Qin; Zhitao Liu; Zi Li; Juanjuan Li; Deepthi S Varma; Qingqing Wan; Jiang Zhao; Xiangdong Min; Xingmeng Han; Min Liu
Journal:  Nutrients       Date:  2018-01-31       Impact factor: 5.717

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