Literature DB >> 33958885

The Association Between Sarcopenic Obesity and Hypertension, Diabetes, and Abnormal Lipid Metabolism in Chinese Adults.

Ting Yin1,2, Jia-Xing Zhang1, Fa-Xuan Wang1,2, Jian-Hua Zhao3, Yu Zhao1,2, Lan Liu1,2, Xiu-Ying Liu1,2, Yu-Hong Zhang1,2, Yi Zhao1,2.   

Abstract

OBJECTIVE: Sarcopenic obesity is associated with several negative health outcomes. However, there are only a few studies on the relationship between SO and metabolic diseases such as diabetes, hypertension, and abnormal lipid metabolism in Chinese adults. The aim of this work was to evaluate the association between SO and hypertension, diabetes, and abnormal lipid metabolism in Chinese adults, and explore the prediction of SO using relevant anthropometric indicators.
MATERIALS AND METHODS: All participants underwent a questionnaire interview for the collection of demographic data. Thereafter, they underwent physical examination for the measurement of anthropometric variables, which was performed using bioelectrical impedance analysis. Biochemical measurements were determined according to standard laboratory procedures used for the evaluation of blood parameters.
RESULTS: We included 14,926 patients aged 35-74 years old. The mean age of the participants was 56.75 ± 9.76 years old, and 39.80% of them were male. The mean body mass index (BMI) was 24.94 ± 3.40 kg/m2, and the overall prevalence of SO was 65.1%. The results showed that shorter people; people with faster heart rate; heavier weight; lower waist circumference (WC), BMI, triglyceride level, total cholesterol, and low-density lipoprotein cholesterol levels; and higher high-density lipoprotein cholesterol level are at risk for SO.
CONCLUSION: The prevalence of SO is high (65.1%) in Chinese adults aged 35-74 years old. The occurrence of SO is related to hypertension, diabetes, and abnormal lipid metabolism. BMI, WC, and waist-hip ratio may be predictive indicators of SO. The incidence of SO may be reduced by timely intervention and health education for persons at risk of the condition.
© 2021 Yin et al.

Entities:  

Keywords:  abnormal lipid metabolism; diabetes mellitus; hypertension; sarcopenic obesity

Year:  2021        PMID: 33958885      PMCID: PMC8096416          DOI: 10.2147/DMSO.S308387

Source DB:  PubMed          Journal:  Diabetes Metab Syndr Obes        ISSN: 1178-7007            Impact factor:   3.168


Introduction

With increasing age, human hormonal levels and body activity decrease, muscle mass and muscle function decline, and abdominal obesity and visceral fat content increase, resulting in sarcopenic obesity (SO).1–3 SO, which reflects a combination of sarcopenia and obesity, is a complex systemic condition that often has a negative impact on body activities. Its pathogenesis may be related to aging or other diseases, and as such can occur in individuals of all age groups.4–6 Studies have shown that SO is closely related to falls and abnormal lipid metabolism in the elderly. The condition has a poor prognosis and leads to an increased risk of disability, cardiovascular disease, and death.7–9 The rapidly increasing morbidity and serious consequences associated with SO are recognized as critical public health risks among the aging population.10,11 Hypertension, which is another global public health problem, has become one of the important causes of death from cardiovascular disease. It is characterized by high disability and mortality rates, which reflect an enormous consumption of medical and social resources. Studies have demonstrated that SO may be related to the occurrence of hypertension, and that fat-to-muscle ratio is a significant predictor of metabolic diseases in Korean adults.12 However, there are only a few studies on the relationship between SO and metabolic diseases such as diabetes, hypertension, and abnormal lipid metabolism in Chinese adults. More studies are needed to explore the association between SO and its pathogenesis and other metabolic diseases to permit the initiation of preventive measures at the level of anthropometric variables. These anthropometric variables can be analyzed to understand the body movement and the nutrition and health status of an individual, particularly to increase the understanding of metabolic diseases. This analysis of anthropometric variables can play a timely warning role in the prevention of hypertension. Thus, the aim of the present study was to evaluate the association between SO and hypertension, diabetes, and abnormal lipid metabolism in Chinese adults, and to explore the appropriate predictive index of SO using relevant anthropometric indicators.

Materials and Methods

Study Design and Participants

This study was the baseline of a population-based cohort study conducted at Ningxia Medical University from March 2018 to May 2019. Participants were recruited through the Ningxia cohort from the China Northwest Cohort, a prospective population study that comprised a sample of 14,926 men and women aged 35 to 74 years old. The inclusion criteria were as follows: male and female adults aged between 35 and 74 years old (born between 1943 and 1982); registered permanent residents of the selected investigation sites (those who stay at home for more than five months throughout the year); persons with no serious physical disability and who are able to communicate normally. All participants met these inclusion criteria and provided written informed consent before participating in the study. All investigations were performed in accordance with the tenets of the Declaration of Helsinki. This study was approved by the Ethical Committee of Ningxia Medical University (ID: 2018–021). The specific participant selection process is outlined in Figure 1.
Figure 1

Respondent screening process for the participants.

Respondent screening process for the participants.

Setting

All participants underwent a questionnaire interview for collection of demographic data and information on living habits, and then a physical examination for measurement of anthropometric variables. After blood samples were sent to the clinical laboratory testing department, biochemical measurements were determined according to standard laboratory procedures. All procedures were performed by trained investigators and all samples were processed by trained and experienced laboratory technicians.

Variables

Demographic Data

After signing the informed consent form, all participants completed a questionnaire to provide information on demographic data such as age, sex, marital status, smoking, and alcohol consumption. Living habits like salt intake and exercise behaviors were assessed to explore the risk factors to health.

Anthropometric Variables

The measurement of the anthropometric variables was performed by well-trained investigators. Body height (cm) was measured using a height bar, with the participant in light clothing and without shoes. Brachial artery blood pressure and pulse were measured using an electronic sphygmomanometer. Each measurement was taken twice; if the measured values were within 0.5 cm of each another, the average value was calculated and used for analysis. If the difference between the two measurements exceeded 0.5 cm, a third measurement was taken. Weight, body mass index (BMI), appendicular skeletal muscle mass (ASM) and other anthropometric variables of the participants were acquired using a bioelectrical impedance analyzer (BIA) (Inbody370 Co., Seoul, Korea) according to standard guidelines. The use of bioelectrical impedance analysis for the measurement of anthropometric variables has gained popularity.13,14 The BIA used in this study calculates the resistance of body tissues by transmission of an electrical signal sent through the hands and feet. According to the manufacturer’s instructions, participants were directed to remove extra clothing items such as shoes, coats, and sweaters, and metal accessories such as earrings, rings, and watches. They were then asked to stand on the balance scale barefoot and grasp the handles of the BIA. The examination takes nearly 30 seconds to complete; the result is displayed upon completion of the procedure.

Biochemical Variables

Blood samples were collected between 8:00 a.m. and 10:00 a.m. following an overnight fasting. The samples were biochemically analyzed using standard laboratory enzymatic methods. The enzymatic methods are optimized for blood biochemical analysis.15,16 These analyses included evaluation of plasma glucose (fasting blood glucose [FBG], mmol/L), total cholesterol (TC, mmol/L), triglyceride (TG, mmol/L), and high-density lipoprotein cholesterol (HDL-C, mmol/L) levels. The serum was centrifuged, aliquoted, and stored at −80°C.

Definitions

Sarcopenia was defined as ASM/height2 (kg/m2) according to the recommendations of the Asian Working Group for Sarcopenia, which suggests that based on BIA measurements, 7.0 kg/m2 is the cut-off value for men and 5.7 kg/m2 is the cut-off value for women.17 According to the World Health Organization, the definition of obesity is a body fat rate greater than 30% for women or greater than 25% for men. Individuals defined as having sarcopenia according to the criteria of the Asian Working Group and concurrent obesity by any of the standard definitions, were considered individuals with SO. The diagnosis of hypertension was based on the recommendations in the Chinese guidelines for the treatment of hypertension in 2005, which defined systolic blood pressure (SBP) ≥140 mmHg and diastolic blood pressure (DBP) ≥90 mmHg as hypertension. The diabetes discussed in this study is type 2 diabetes, and the diagnosis defined by the American Diabetes Association in 2010, which is fasting plasma glucose ≥7.0 mmol/l of FBG, was selected. The diagnosis for dyslipidemia used in this study refers to the 2016 (revised) guidelines for the prevention and treatment of dyslipidemia in Chinese adults. Patients with hypercholesterolemia (TC ≥ 5.20 mmol/L), hypertriglyceridemia (TG ≥ 1.70 mmol/L) or low high-density lipoprotein cholesterolemia (HDL-C <1.00 mmol/L) were diagnosed with dyslipidemia.

Statistical Analyses

Data are presented as group mean ± standard deviation (SD) unless otherwise stated. All analyses were performed separately for women and men. Chi-square tests and Student’s t-tests were used to analyze the prevalence of SO for different BMI, waist circumference (WC), and hip circumference levels. Logistic regression model was used to analyze the influence of predictive variables on the classification results. A receiver operating characteristic (ROC) curve adjusted for potential confounding variables was constructed, using the point on the ROC curve closest to (0, 1) as a criterion to calculate the cut-off for assessing the risk for SO according to the anthropometric variables. All analyses were performed using SPSS statistical software version 26.0. All tests were two-tailed; p < 0.05 was considered statistically significant.

Results

Participants

A total of 14,926 persons (8978 women and 5948 men) aged 35–74 years old volunteered to participate in this study and underwent all the measurements for further analysis. The mean age of the respondents was 56.75 ± 9.76 years old and 39.80% of them were male. The mean BMI of the respondents was 24.94 ± 3.40 kg/m2, 67.3% had a primary school education or had never been to school, 15.1% were current smokers, and 24.3% had an alcohol consumption habit. Figure 1 shows the prevalence of SO according to sexual parameters. Of the included participants, 65.1% (9721/14,926) had SO according to the previously outlined definition. Most of the participants that had SO were female, and their mean age was 58.59 ± 9.59 years old. The proportion of participants who had hypertension, diabetes, and abnormal lipid metabolism was 21.1%, 5.0%, and 57.6%, respectively.

Outcome Data and Main Results

Main Characteristics of the Participants According to the Presence of Sarcopenic Obesity

The main characteristics of the female and male reference groups are outlined in Table 1. The SO and non-SO groups showed differences in sex, age, education level, weight, height, WC, HC, SBP, DBP, pulse, BMI, waist-to-hip ratio (WHR), ASM, ASMI, FBG, TG, TC, HDL-C and LDL-C (p < 0.05). In addition, current smoking status, alcohol consumption, obesity, hypertension, diabetes, and abnormal lipid metabolism were different between two groups (p < 0.05), whereas marital status, income level, and exercise habit showed no differences (p > 0.05) [Table 1].
Table 1

Participants Characteristic According to the Presence of SO

VariablesSOWithout SOp value
Males (n=3298)Females (n=6423)Total (n=9721)Males (n=2650)Females (n=2555)Total (n=5205)
Demographic characteristics
Age (years)58.37±9.5255.84±9.4056.70±9.5258.85±9.5754.77±10.3356.85±10.210.394
35–44318 (9.6)807 (12.6)1125 (11.6)254 (9.2)470 (18.4)715 (13.7)<0.001
45–54857 (26.0)2204 (34.3)3061 (31.5)641 (24.2)895 (35.0)1536 (29.5)
55–641009 (30.6)1951 (30.4)2960 (30.4)819 (30.9)587 (23.0)1406 (27.1)
65–741114 (33.8)1461 (22.7)2575 (26.5)945 (35.7)603 (23.6)1548 (29.7)
Marital status
Married3136 (95.1)5981 (91.7)9027 (92.9)2523 (95.2)2346 (91.8)4869 (93.5)0.332
Widowed109 (3.3)481 (7.5)590 (6.1)84 (3.2)198 (7.7)282 (5.4)
Divorce24 (0.7)22 (0.3)46 (0.5)15 (0.6)5 (0.2)20 (0.4)
Unmarried29 (0.9)29 (0.5)58 (0.5)28 (1.0)6 (0.3)34 (0.7)
Education
Not been to school741 (22.5)2704 (42.1)3445 (35.4)690 (26.0)1000 (391)1690 (32.5)<0.001
Primary school1242 (37.7)1951 (30.4)3193 (32.8)943 (35.6)767 (30.0)1710 (32.9)
Junior high school1123 (34.0)1607 (25.0)2730 (28.2)882 (33.3)711 (27.8)1593 (30.6)
Senior high school and above192 (5.8)161 (2.5)353 (3.6)135 (5.1)77 (3.0)212 (4.0)
Income (RMB/year)
Less than 10,000815 (24.7)1569 (24.4)2384 (24.5)658 (24.8)595 (23.3)1253 (24.0)0.114
10,000~1920 (58.2)3811 (59.3)5731 (59.0)1620 (61.1)1519 (59.4)3139 (60.3)
50,000~345 (10.5)558 (8.7)903 (9.3)229 (8.6)258 (10.1)487 (9.4)
More than 100,000218 (6.6)485 (7.6)703 (7.2)143 (5.4)183 (7.2)326 (6.3)
Exercise(days/week)
≦11888 (57.2)3743 (58.3)5631 (57.9)1553 (58.6)1485 (58.1)3038 (58.4)0.680
2~3263 (8.0)569 (8.8)832 (8.6)199 (7.5)225 (8.8)424 (8.1)
4~5337 (10.2)659 (10.3)996 (10.2)287 (10.8)266 (10.4)553 (10.6)
6~7810 (24.6)1452 (22.6)2262 (23.3)611 (23.1)579 (22.7)1190 (22.9)
Current Smoking (yes), n (%)1103 (33.4)120 (1.9)1223 (12.6)999 (37.7)28 (1.1)1027 (19.7)<0.001
Alcohol consumption (yes), n (%)1388 (42.1)917 (14.3)2305 (23.7)937 (35.4)383 (15.0)1320 (25.4)0.025
Obesity, n (%)3298 (100.0)6423 (100.0)9721 (100.0)414 (15.6)550 (21.5)964 (18.5)<0.001
Hypertension, n (%)819 (24.8)1494 (23.3)2313 (23.8)439 (16.6)403 (15.8)842 (16.2)<0.001
Diabetes, n (%)199 (6.0)340 (5.3)539 (5.5)103 (3.9)102 (4.0)205 (3.9)<0.001
Abnormal lipid metabolism, n (%)2104 (63.8)3835 (59.7)5939 (61.1)1164 (43.9)1175 (46.0)2339 (44.9)<0.001
Anthropometric variables
Weight (kg)74.79±8.7863.85±8.0167.56±9.7761.81±7.9752.78±6.5957.38±8.61<0.001
Height (m)1.66±0.061.56±0.061.59±0.081.66±0.671.56±0.661.61±0.84<0.001
WC (cm)95.03±8.2389.49±7.7791.37±8.3580.70±6.8877.35±5.8979.06±6.63<0.001
HC (cm)99.02±4.0595.29±4.3096.56±4.5792.04±3.7988.63±3.4790.36±4.02<0.001
SBP (mm Hg)139.39±18.91136.69±19.33137.60±19.23131.77±18.90130.58±19.78131.19±19.34<0.001
DBP (mm Hg)86.95±12.7783.63±12.2084.76±12.4981.21±12.5576.65±12.1480.44±12.38<0.001
Pulse (bpm)74.06±12.1777.69±11.8876.45±12.1072.51±12.1878.17±12.0975.28±12.46<0.001
BMI (kg/m2)27.10±2.5526.26±2.8626.54±2.7922.29±2.2021.61±2.1321.95±2.20<0.001
WHR0.96±0.560.94±0.050.95±0.540.88±0.050.87±0.050.87±0.50<0.001
ASM (kg)22.21±2.7016.44±2.1719.40±3.6220.67±3.2115.26±2.7418.02±4.03<0.001
ASMI (kg/m2)8.03±0.606.74±0.607.18±0.867.43±0.756.21±0.746.83±0.96<0.001
Biochemical variables
FBG (mmol/L)5.76±1.675.62±1.565.67±1.605.66±1.825.55±1.755.61±1.790.041
TG (mmol/L)1.89±1.261.79±1.111.82±1.171.43±1.131.51±1.101.47±1.12<0.001
TC (mmol/L)4.82±1.175.03±1.024.96±1.084.57±0.964.79±0.984.68±0.98<0.001
HDL-C (mmol/L)1.26±0.341.39±0.341.35±0.351.32±0.371.41±0.331.37±0.36<0.001
LDL-C (mmol/L)2.80±0.892.92±0.802.88±0.832.72±0.982.78±0.792.75±0.89<0.001

Note: Bold indicates statistical significance.

Participants Characteristic According to the Presence of SO Note: Bold indicates statistical significance.

The Correlation Between Sarcopenic Obesity and Hypertension, Diabetes, and Abnormal Lipid Metabolism

Table 1 also shows that there is positive correlation between SO and hypertension, diabetes, and abnormal lipid metabolism in the entire study population (p < 0.05). The positive correlation between SO and hypertension, diabetes, and abnormal lipid metabolism showed statistically significant difference in both males and females. Logistic regression was used to analyze the influencing factors. The results shown that gender, SBP, DBP, FBG, TC, TG and HDL-C were the influencing factors for SO, and diabetes mellitus (1.251, 95% CI: 1.034–1.514), hypertension (1.157, 95% CI: 1.045–1.281) and abnormal lipid metabolism (1.327, 95% CI: 1.209–1.458) were the risk factors for SO [Table 2]. Finally, when adjustment for age, sex, education, smoking, alcohol consumption, diabetes, hypertension, abnormal lipid metabolism were added into the model, with each of the SO-influencing indicators still having significant ORs for BMI, WC, and WHR [Table 3].
Table 2

Logistic Regression of the Influencing Factors of SO

VariablesβS.E.WaldOR (95% CI)p value
Sex0.7650.041354.0632.149 (1.984, 2.327)<0.001
Age−0.0410.0233.1270.960 (0.918, 1.004)0.077
SBP0.0100.00243.9011.010 (1.007, 1.013)<0.001
DBP0.0170.00256.9471.017 (1.013, 1.022)<0.001
FBG−0.0300.0126.1730.970 (0.947, 0.994)0.013
TC0.1740.03229.8221.190 (1.118, 1.266)<0.001
TG0.1590.02348.3421.172 (1.121, 1.226)<0.001
HDL-C−0.4420.06644.9804.643 (4.565, 0.731)<0.001
LDL-C−0.0310.0310.9820.970 (0.912, 1.031)0.322
Education0.0180.0240.5251.018 (0.970, 1.067)0.469
Diabetes0.2240.0975.3021.251 (1.034, 1.514)0.021
Hypertension0.1460.0527.8471.157 (1.045, 1.281)0.005
Abnormal lipid metabolism0.2830.04835.2971.327 (1.209, 1.458)<0.001
Constant−3.7040.220282.254

Note: Bold indicates statistical significance.

Table 3

Multivariable Association of Participants’ Characteristics with SO

VariablesModel 1Model 2Model 3Model 4
OR (95% CI)p valueOR (95% CI)p valueOR (95% CI)p valueOR (95% CI)p value
SBP1.000 (0.996, 1.004)0.9360.994 (0.990, 0.999)0.0180.994 (0.990, 0.999)0.0170.996 (0.991, 1.000)0.068
DBP0.995 (0.989, 1.002)0.1491.003 (0.996, 1.010)0.4301.003 (0.996, 1.010)0.4711.003 (0.996, 1.010)0.358
Pulse1.009 (1.004, 1.014)<0.0011.001 (0.996, 1.006)0.5781.001 (0.996, 1.006)0.6441.001 (0.996, 1.006)0.598
FBG0.961 (0.931, 0.993)0.0160.965 (0.933, 0.999)0.0430.966 (0.934, 1.000)0.0480.966 (0.932, 1.002)0.066
TG0.981 (0.932, 1.032)0.4520.960 (0.910, 1.012)0.1310.963 (0.913, 1.016)0.1680.966 (0.913, 1.023)0.236
TC1.103 (1.012, 1.202)0.0251.113 (1.012, 1.224)0.0271.097 (0.998, 1.207)0.0561.085 (0.983, 1.198)0.105
HDL-C1.283 (1.068, 1.541)0.0081.068 (0.881, 1.294)0.5051.067 (0.881, 1.293)0.5061.067 (0.877, 1.298)0.516
LDL-C1.003 (0.921, 1.091)0.9520.955 (0.865, 1.056)0.3710.974 (0.882, 1.075)0.6010.979(0.888, 1.080)0.670
WC0.828 (0.803, 0.854)<0.0011.076 (1.034, 1.119)<0.0011.079 (1.038, 1.122)<0.0011.079 (1.038, 1.122)<0.001
WHR1.338 (1.296, 1.381)<0.0011.055 (1.015, 1.096)<0.0011.055 (1.016, 1.096)0.0061.056 (1.016, 1.097)0.005
BMI2.773 (2.623, 2.933)<0.0012.060 (1.936, 2.192)<0.0012.061 (1.937, 2.193)<0.0012.070 (1.944, 2.203)<0.001

Notes: Bold indicates statistical significance. Model 1 has no controlled variables; Model 2 adjusted for age, sex, education; Model 3 adjusted for Model 2 and smoking, alcohol consumption; Model 4 adjusted for Model 3 and diabetes, hypertension, abnormal lipid metabolism.

Logistic Regression of the Influencing Factors of SO Note: Bold indicates statistical significance. Multivariable Association of Participants’ Characteristics with SO Notes: Bold indicates statistical significance. Model 1 has no controlled variables; Model 2 adjusted for age, sex, education; Model 3 adjusted for Model 2 and smoking, alcohol consumption; Model 4 adjusted for Model 3 and diabetes, hypertension, abnormal lipid metabolism.

The Area Under the Curve of Different Anthropometric Variables in the Evaluation of Sarcopenic Obesity

The prevalence of SO was 55.40% in males and 71.50% in females. The area under the curve (AUC) of weight, height, WC, WHR, BMI, SBP, DBP, pulse, FBG, TG, TC, HDL-C and LDL-C for SO showed statistical difference. These indicators also showed significant difference in males; however, pulse showed no statistical difference in females. Among these indicators, BMI was the best variable for predicting SO in both males and females; the cut-off value was 24.45 for males and 23.45 for females. WC and WHR can also be predictors for SO, with 85.95 and 0.91 as the cut-off values for males and 82.25 and 0.90 as the cut-off values for females, respectively [Table 4], [Figure 2].
Table 4

AUC of Different Anthropometric Variables Evaluating SO

Total (n=14,926)Male (n=5948)Female (n=8978)
AUC (95% CI)Cut-OffSensitivity (%)Specificity (%)AUC (95% CI)Cut-OffSensitivity (%)Specificity (%)AUC (95% CI)Cut-OffSensitivity (%)Specificity (%)
Weight0.786 (0.778, 0.794) **60.0576.6064.860.866 (0.857, 0.876)**67.1579.6476.830.863 (0.854, 0.872)**56.7581.1474.33
Height0.425 (0.415, 0.436) **1.6232.5554.850.484 (0.468, 0.500) *1.7122.3173.900.484 (0.469, 0.499) *1.5831.7062.95
WC0.883 (0.877, 0.889) **84.2580.0779.700.915 (0.908, 0.923) **85.9587.6279.590.903 (0.895, 0.910)**82.2582.9681.03
WHR0.844 (0.837, 0.851) **0.9176.7776.620.867 (0.857, 0.876) **0.9178.4879.630.841 (0.832, 0.851)**0.9078.9474.37
BMI0.912 (0.907, 0.917) **23.7584.9180.410.931 (0.925, 0.938) **24.4585.3284.640.918 (0.911, 0.924)**23.4584.4281.97
SBP0.604 (0.593, 0.614) **131.5059.4455.880.624 (0.609, 0.639) **135.5055.9763.290.599 (0.585, 0.613) **123.5073.6741.64
DBP0.602 (0.592, 0.613) **79.5066.1148.960.631 (0.616, 0.646) **83.5058.3059.920.598 (0.584, 0.612) **79.5063.0351.92
Pulse0.530 (0.520, 0.541) **71.5064.3641.070.539 (0.524, 0.555) **71.5054.8851.770.489 (0.475, 0.504)80.5035.8660.92
FBG (mmol/L)0.530 (0.519, 0.540) **5.5639.8964.430.536 (0.520, 0.551) **5.5644.5161.480.539 (0.525, 0.53) **5.1761.8144.29
TG0.626 (0.616, 0.636) **1.2565.9053.200.642 (0.627, 0.657) **1.3063.4659.230.610 (0.596, 0.624) **1.4852.9663.87
TC0.580 (0.569, 0.590) **4.6063.0749.140.572 (0.556, 0.587) **4.5459.1951.860.566 (0.552, 0.581) **4.6763.6047.20
HDL-C (mmol/L)0.479 (0.469, 0.490) **1.3446.8949.440.442 (0.427, 0.458) **1.2152.7237.790.474 (0.460, 0.489) **1.5923.7271.90
LDL-C (mmol/L)0.550 (0.540, 0.561) **2.5763.2144.250.534 (0.518, 0.550) **2.4465.5539.600.551 (0.537, 0.565) **2.8053.0554.83

Notes: *Indicates p-value from Pearson correlation<0.05, **indicates p-value from Pearson correlation<0.001. Bold indicates AUC>0.85.

Figure 2

ROC curves for total participants (A), male (B) and female (C) in predicting sarcopenic obesity according to BMI, WC, WHR (GraphPad Prism 8 used to create the artwork).

AUC of Different Anthropometric Variables Evaluating SO Notes: *Indicates p-value from Pearson correlation<0.05, **indicates p-value from Pearson correlation<0.001. Bold indicates AUC>0.85. ROC curves for total participants (A), male (B) and female (C) in predicting sarcopenic obesity according to BMI, WC, WHR (GraphPad Prism 8 used to create the artwork).

Discussion

In this study, we investigated the associations between SO and hypertension, diabetes, and abnormal lipid metabolism. After controlling for potential confounders, we found that hypertension was significantly associated with the risk of sarcopenia. We also evaluated the prevalence of SO in Chinese adults and found that the overall prevalence of SO was 65.1%. The prevalence of SO has been reported to be higher in patients with chronic diseases such as hypertension, diabetes, abnormal lipid metabolism.18–21 The results of this study also indicate that the participants in the SO group were older than the those in the non-SO group, suggesting that increasing age may be a risk factor for the occurrence of SO.22,23 The participants in the SO group were shorter; had faster heart rate; heavier weight; lower WC, BMI, TG, TC, LDL-C, and higher HDL-C; and lower education level than those in the non-SO group. This may be related to decreased hormone levels, decreased mobility, and decreased protein intake and synthesis caused by aging. Early education and appropriate intervention in the elderly may reduce or delay the occurrence of SO.24–26 Many studies have shown that the occurrence of SO is related to cardiovascular diseases and metabolic diseases such as hypertension, diabetes, and abnormal lipid metabolism.27,28 The results of the present study suggest that hypertension, diabetes, and elevated TC are risk factors for the occurrence of SO. Loss of muscle represents the reduction of target tissues for insulin action, and leads to insulin resistance, which then leads to obesity, metabolic syndrome, hypertension, and other diseases. In both frailty and sarcopenia, there is dysfunction and degeneration of muscle and adipose tissue. Studies have shown that loss of muscle mass and strength in adults is associated with metabolic disorders and dysfunction, while insulin resistance and higher ectopic fat accumulation may play a role.29,30 Glucocorticoid receptors activate and promote progressive loss of cardiac myocyte apoptosis during heart failure. In addition, myocardial apoptosis is also present in the skeletal muscle of patients with congestive heart failure. This apoptosis exacerbates muscle atrophy, weakness, and decreased exercise tolerance, with a pathophysiological process similar to that of SO.31,32 In obese adipose tissue, adipose cells undergo hypertrophy and hyperplasia, and activate, causing the proinflammatory macrophages and other immune cells, as well as aging cells and immune cells, to release cytokines and chemokines that lead to enhanced secretion of proinflammatory myokine. Also, myokines induce inflammatory state in muscles as a result of abnormal adipose tissue functions. These proinflammatory muscle growth factors can be induced through autocrine/paracrine manner and cause muscle dysfunction, triggering and sustaining the development of the SO.33 Moreover, multiple factors in the inflammatory response are closely associated with chronic conditions including obesity,34 metabolic syndrome,35 type 2 diabetes36,37 and coronary heart disease,38 which all promote to SO. Studies have shown that inflammatory factors are associated with type 2 diabetes, and the increase in white blood cells is mainly due to neutrophil count, while the neutrophil to lymphocyte ratio (NLR) in type 2 diabetes patients is increased compared with the healthy control group. Neutrophilia can respond quickly to inflammatory stimuli and rapidly increase neutrophil counts. At the same time, interleukin levels in inflammatory conditions lead to neutrophilia, which together lead to increased NLR.36,39 This study was mainly focused on rural areas, where the prevalence of diabetes and SO are both relatively low. At present, the association between hypertension and SO is mentioned in only a few reports.40 The findings of the present study showed that hypertension has a significant association with SO. In this study, the DBP and SBP of the SO group were higher than those of the non-SO group, suggesting that blood pressure may be a predictive indicator of SO. However, this finding needs to be confirmed by further investigation. SO is often accompanied by functional impairment and physical disability, which results in a decrease in anti-inflammatory factors (also known as myokines) produced by muscle contractions. The relative deficiency of anti-inflammatory factors in SO may increase the risk of cardiovascular and metabolic diseases in individuals. However, there are still some disputes regarding the evaluation criteria for SO, and the forecast indicators in the proposed criteria are not the same.41,42 Some studies indicate that anthropometric data such as WC and BMI are important indicators for predicting SO.43,44 The results of the present study suggest that BMI is the best indicator for predicting the occurrence of SO; WC and WHR were also found to be suitable predictors for SO. Since these measures are both anthropometric indicators and can be conveniently measured and calculated during general physical examination, we recommend that these indexes may be used as predictive indicators for SO.

Limitations

The present study had some limitations. First, we only used data acquired using the BIA to measure sarcopenia; however, the diagnosis of the condition may include stride speed and grip at the same time. Second, the data for this study were the baseline of a cohort study, which precluded our ability to identify cause-effect association, particularly in the association between SO and other diseases. Despite these limitations, we investigated the prevalence of SO in 35–74-year-old Chinese adults, and identified some factors associated with SO. Our findings will provide some evidence and basis for subsequent research on SO.

Conclusion

This study showed that prevalence of SO is high (65.1%) in Chinese adults aged 35–74 years old. The results also indicate that the occurrence of SO is related to hypertension, diabetes, and abnormal lipid metabolism. BMI, WC, and WHR were found to be possible predictive indicators of SO.
  42 in total

1.  Phase angle from bioelectrical impedance analysis: population reference values by age, sex, and body mass index.

Authors:  Anja Bosy-Westphal; Sandra Danielzik; Ralf-Peter Dörhöfer; Wiebke Later; Sonja Wiese; Manfred J Müller
Journal:  JPEN J Parenter Enteral Nutr       Date:  2006 Jul-Aug       Impact factor: 4.016

2.  Asian Working Group for Sarcopenia: 2019 Consensus Update on Sarcopenia Diagnosis and Treatment.

Authors:  Liang-Kung Chen; Jean Woo; Prasert Assantachai; Tung-Wai Auyeung; Ming-Yueh Chou; Katsuya Iijima; Hak Chul Jang; Lin Kang; Miji Kim; Sunyoung Kim; Taro Kojima; Masafumi Kuzuya; Jenny S W Lee; Sang Yoon Lee; Wei-Ju Lee; Yunhwan Lee; Chih-Kuang Liang; Jae-Young Lim; Wee Shiong Lim; Li-Ning Peng; Ken Sugimoto; Tomoki Tanaka; Chang Won Won; Minoru Yamada; Teimei Zhang; Masahiro Akishita; Hidenori Arai
Journal:  J Am Med Dir Assoc       Date:  2020-02-04       Impact factor: 4.669

Review 3.  The implications of sarcopenia and sarcopenic obesity on cardiometabolic disease.

Authors:  Tae Nyun Kim; Kyung Mook Choi
Journal:  J Cell Biochem       Date:  2015-07       Impact factor: 4.429

4.  The Impact of Age on the Prevalence of Sarcopenic Obesity in Bariatric Surgery Candidates.

Authors:  Judit Molero; Violeta Moizé; Lilliam Flores; Ana De Hollanda; Amanda Jiménez; Josep Vidal
Journal:  Obes Surg       Date:  2020-06       Impact factor: 4.129

5.  Oxidative stress is increased in sarcopenia and associated with cardiovascular disease risk in sarcopenic obesity.

Authors:  Francesco Bellanti; Antonino D Romano; Aurelio Lo Buglio; Valeria Castriotta; Giuseppe Guglielmi; Antonio Greco; Gaetano Serviddio; Gianluigi Vendemiale
Journal:  Maturitas       Date:  2017-12-05       Impact factor: 4.342

6.  Sarcopenic obesity and its association with respiratory disease incidence and mortality.

Authors:  Fanny Petermann-Rocha; Shuai Yang; Stuart R Gray; Jill P Pell; Carlos Celis-Morales; Frederick K Ho
Journal:  Clin Nutr       Date:  2020-03-12       Impact factor: 7.324

Review 7.  Sarcopenia and sarcopenic obesity.

Authors:  Kyung Mook Choi
Journal:  Korean J Intern Med       Date:  2016-11-01       Impact factor: 2.884

8.  The Association between Red Blood Cell Distribution Width and Sarcopenia in U.S. Adults.

Authors:  Junghoon Kim; Jeong-Soo Im; Chang Hyu Choi; Chul Hyun Park; Jae Ik Lee; Kuk Hui Son; Yoon-Hyeong Choi
Journal:  Sci Rep       Date:  2018-07-31       Impact factor: 4.379

Review 9.  Lifestyle Interventions with a Focus on Nutritional Strategies to Increase Cardiorespiratory Fitness in Chronic Obstructive Pulmonary Disease, Heart Failure, Obesity, Sarcopenia, and Frailty.

Authors:  Hayley Billingsley; Paula Rodriguez-Miguelez; Marco Giuseppe Del Buono; Antonio Abbate; Carl J Lavie; Salvatore Carbone
Journal:  Nutrients       Date:  2019-11-21       Impact factor: 5.717

10.  The increased risk of sarcopenia in patients with cardiovascular risk factors in Suburb-Dwelling older Chinese using the AWGS definition.

Authors:  Peipei Han; Hairui Yu; Yixuan Ma; Li Kang; Liyuan Fu; Liye Jia; Xiaoyu Chen; Xing Yu; Lin Hou; Lu Wang; Wen Zhang; Haifang Yin; Kaijun Niu; Qi Guo
Journal:  Sci Rep       Date:  2017-08-29       Impact factor: 4.379

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  4 in total

1.  The Difference in Body Type May Modify the Relationship Between Dietary Mineral Intake and Hypertension Among Korean Adults.

Authors:  Xiaohua Ren; Roujun Pan; Zhipeng Li; Lianping He
Journal:  Biol Trace Elem Res       Date:  2022-06-04       Impact factor: 3.738

Review 2.  The Critical Role of Oxidative Stress in Sarcopenic Obesity.

Authors:  Andrea Gonzalez; Felipe Simon; Oscar Achiardi; Cristian Vilos; Daniel Cabrera; Claudio Cabello-Verrugio
Journal:  Oxid Med Cell Longev       Date:  2021-10-12       Impact factor: 6.543

3.  Association of Obesity, Sarcopenia, and Sarcopenic Obesity With Hypertension in Adults: A Cross-Sectional Study From Ravansar, Iran During 2014-2017.

Authors:  Yahya Pasdar; Mitra Darbandi; Shahab Rezaeian; Farid Najafi; Behrooz Hamzeh; Amir Bagheri
Journal:  Front Public Health       Date:  2022-02-02

4.  Endothelin-1-mediated miR-let-7g-5p triggers interlukin-6 and TNF-α to cause myopathy and chronic adipose inflammation in elderly patients with diabetes mellitus.

Authors:  Chung-Huang Tsai; Pei-Ju Huang; I T Lee; Chien-Min Chen; Min Huan Wu
Journal:  Aging (Albany NY)       Date:  2022-04-25       Impact factor: 5.682

  4 in total

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