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Association of body mass index and waist circumference with type 2 diabetes mellitus in older adults: a cross-sectional study

Abstract

Background

The prevalence of obesity and diabetes is rising. The aim of this study was to determine the association of body mass index (BMI) and waist circumference (WC) with type 2 diabetes mellitus (T2DM) in the elderly and to compare the discriminatory abilities of BMI, WC and other anthropometric indicators, including waist-to-height ratio (WHtR), body adiposity estimator (BAE) and body roundness index (BRI) for T2DM.

Methods

This cross-sectional study included 69,388 subjects aged ≥ 60 years living in Xinzheng, Henan Province, from January to December 2020. The data came from the residents’ electronic health records of the Xinzheng Hospital Information System. Logistic regression was used to examine the relationships. Fully adjusted models adjusted for age, sex, place of residence, alcohol consumption, smoking, physical exercise, SBP and RHR. The area under the receiver operating characteristic curve (AUC) was used to compare the discriminatory ability of different anthropometric indicators for T2DM under the influence of potential risk factors.

Results

After adjusting for multiple covariates, compared with the first BMI quintile, the odds ratios (ORs) and 95% confidence intervals (CIs) from the second to fifth quintile for T2DM were 1.416 (1.335–1.502), 1.664 (1.570–1.764), 1.879 (1.774–1.990) and 2.156 (2.037–2.283), respectively. Compared with the first WC quintile, the ORs and 95% CIs from the second to fifth quintiles for T2DM were 1.322 (1.244–1.404), 1.549 (1.459–1.643), 1.705 (1.609–1.807) and 2.169 (2.048–2.297), respectively. Among men, compared with other anthropometric indicators (BMI, WHtR, BAE and BRI), WC showed the highest AUC (AUC: 0.629; 95% CI: 0.622–0.636). Among women, the AUCs of BMI (AUC: 0.600; 95% CI: 0.594–0.606), WC (AUC: 0.600; 95% CI: 0.593–0.606) and BAE (AUC: 0.600; 95% CI: 0.594–0.607) were similar, and the AUCs of BMI, WC and BAE were higher than WHtR, BRI.

Conclusions

All anthropometric indicators were positively associated with T2DM. In men, WC with the strongest positive association with T2DM was the best predictor of T2DM. In women, BMI was most strongly associated with T2DM, and the predictive powers of BMI, WC and BAE were similar. After adjusting the potential confounding factors including age, sex, place of residence, alcohol consumption, smoking, physical exercise, SBP and RHR, the effect of these factors was eliminated, the findings were independent of the covariates considered.

Peer Review reports

Background

In recent years, diabetes has been a substantial public health burden worldwide. The global prevalence of diabetes has reached 10.5% (536.6 million people) and will reach 12.2% (783.2 million people) by 2045. Middle-income countries had the largest increase in the prevalence of diabetes. The economic cost was $966 billion in 2021 and will be $1,054 billion in 2045 [1]. The prevalence of diabetes in Chinese adults was 12.8% (ADA criteria including the addition of HbA1c) in 2017. The total number of diabetes patients in mainland China was approximately 129.8 million (70.4 million men and 59.4 million men). The prevalence of diabetes was 28.8% in individuals 60–69 years old and 31.8% in individuals over 70 years old [2].

Diabetes can cause many complications: macrovascular complications, including coronary heart disease, stroke and peripheral vascular disease, and microvascular complications, such as end-stage renal disease, retinopathy and neuropathy, and lower-extremity amputations [3]. The risks of all-cause [4] and cardiovascular disease (CVD) mortality [5] were significantly increased in patients with diabetes. Meanwhile, the quality of life of people with diabetes may decrease [6].

Diabetes has multiple risk factors, such as overweight, obesity, unhealthy diet, poor lifestyle habits, and increased age [7,8,9,10]. In recent years, the proportion of people with obesity (BMI ≥ 30 kg/m2) has been rising substantially worldwide [11]. The prevalence of overweight (25 kg/m2 ≤ BMI < 30 kg/m2) and obesity (BMI ≥ 30 kg/m2) among Chinese adults was 28.1% and 5.2%, respectively [12]. The prevalence of central obesity [waist circumference (WC) ≥ 90 in males and ≥ 85 in females] in Chinese adults was 29.1% (28.6% in males and 29.6% in females), and the estimated total number was 277.8 million (140.1 million males and 137.7 females) [13].

Some articles have studied the relationship between obesity and type 2 diabetes mellitus (T2DM). However, the relationship between obesity and T2DM has always been estimated by grouping body mass index (BMI) or waist circumference (WC), so it is difficult to obtain the precise dose–response relationship. Few studies have examined the interaction between BMI and WC for T2DM. Therefore, this research studied the relationship between BMI and WC and T2DM in elderly individuals, including the dose–response relationship based on restricted cubic spline plots and the additive interaction between WC and BMI for T2DM. The receiver operating characteristic curve (ROC) was used to compare the predictive ability of WC, BMI and other anthropometric indicators for T2DM, including WHtR, BAE and BRI. These indicators have recently been used to study cardiovascular disease, hypertension, mortality and so on [14, 15], so we calculated and analyzed these indicators and compared these indicators with BMI and WC.

Method

Population

The subjects of this cross-sectional study were adults aged ≥ 60 years in Xinzheng, Henan Province, Central China. The data came from the residents' electronic health records in the Xinzheng Hospital Information System from January to December 2020. Doctors set up health records for each resident at their first hospital visit or health examination, and participants aged 60 or older could receive free health examinations. At the start of the study, 70,161 elderly adults were eligible for the study. We excluded participants with the following conditions: (1) missing information for marital status, drinking, smoking, exercise, resting heart rate (RHR), systolic blood pressure (SBP), diastolic blood pressure (DBP), WC or BMI (n = 532); (2) the values of the variables above were illogical (n = 241). Ultimately, the study included 69,388 participants. The data screening flow chart is presented in Supplementary Fig. 1. Informed consent was obtained from the subjects, and this study was approved by the Ethics Committee of Zhengzhou University (Reference Number: ZZUIRB2019-019).

Data collection

Demographic and clinical information was collected at the health checkup for participants. Demographic information included sex (male/female), age, place of residence (urban/rural), marital status, alcohol consumption, smoking, and physical exercise. Smoking included never smokers, former smokers and current smokers. Alcohol consumption and physical exercise were divided into four categories: never, once in a while, more than once a week and every day. Clinical data included anthropometric measurements, laboratory investigations, and self-reported disease history. Participants wearing light clothing took off their shoes, and then their weight and height were measured. BMI was calculated as weight in kilograms divided by the square of height in meters. WC was measured at the midpoint of the distance between the lowest costal ridge and the upper border of the iliac crest.

Other anthropometric indicators included WHtR, BAE and BRI.

WHtR was calculated by dividing WC by height, BAE = -44.988 + (0.503 × age) + (10.689 × sex) + (3.172 × BMI)-(0.026 × (BMI)2) + (0.181 × BMI × sex)-(0.02 × BMI × age)-(0.005 × (BMI)2 × sex) + (0.00021 × (BMI)2 × age), male = 0 and female = 1, and age is in years [16]. BRI = 364.2–365.5 × {1-[(WC/2π)2/(0.5height)2]}1/2 [17].

After participants fasted for 8 h, blood samples were collected to measure blood lipids and blood sugar. After participants had remained sitting for at least five minutes at rest, the SBP, DBP and radial pulse rate of the participants were measured twice by an electronic sphygmomanometer (Omron HEM-7125, Kyoto, Japan), and the mean value was recorded as the final result.

Definition of T2DM

T2DM was defined as having a self-reported T2DM history, using insulin or oral hypoglycemic agents, or having FPG ≥ 7.0 mmol/L [18].

Statistical analysis

Continuous variables were described as the means and standard deviations (SDs). Categorical variables are presented as numbers and proportions. The chi-square test or the Kruskal–Wallis test for categorical variables and ANOVA for continuous variables was used to compare the difference between quintiles of BMI or WC. The associations of BMI and WC with T2DM were analyzed in sex-specific quintiles by a logistic regression model, and ORs with 95% CIs of BMI and WC in categories and continuous variables were expressed in separate models. Model 1 was unadjusted. Model 2 adjusted for age and sex. Model 3 adjusted for the potential confounders, including age, sex, place of residence, alcohol consumption, smoking, physical exercise, SBP, RHR, because these potential confounders might affect the true relationships between the corresponding indicators and diabetes. Some studies have suggested a possible link between alcohol consumption and obesity and diabetes [19, 20], so we adjusted for that in our analysis. The dose–response association and the potentially nonlinear relationship of continuous BMI and WC with T2DM were explored by restricted cubic spline models with four knots. The stratified analysis was performed by sex subgroup using a logistic regression model to test the consistency of these relationships. We also performed additive interaction analysis between BMI and WC for T2DM with BMI and WC analyzed in two categories (BMI: BMI < 25 kg/m2 and BMI ≥ 25 kg/m2 [21]; WC: WC < 85 cm in females and < 90 cm in males, WC ≥ 85 cm in females and ≥ 90 in males [22]). We evaluated the existence of additive interactions by calculating the relative excess risk due to interaction (RERI), attributable proportion due to interaction (AP) and synergy index (S). RERI > 0, AP > 0 or S > 1 was considered a statistically significant additive interaction. Finally, the receiver operating characteristic (ROC) curve and related area under the ROC curve (AUC) were used to compare the capability of BMI, WC and other anthropometric indicators, including WHtR, BAE and BRI, to diagnosis T2DM, and the logistic regression model was used to estimate the related ORs and 95% CIs of WHtR, BAE and BRI for T2DM after adjusting for age, sex, place of residence, alcohol consumption, smoking, physical exercise, SBP, RHR. The Cohen’s d was utilized to estimate the effect size of anthropometric indicators [23]. Statistical analyses were performed using SPSS V 21 and R V 4.0.3. P < 0.05 with two-sided tests was considered statistically significant.

Results

A total of 69,388 participants were enrolled, including 37,479 women and 31,909 men. The mean (SD) age was 71.4 (6.9) years. A total of 18,756 participants had T2DM, and the incidence rate was 27.0%. The baseline characteristics of the participants according to different BMIs and WC quintiles are shown in Table 1 and Supplementary Table 1. As BMI increases, the incidence of T2DM increases, SBP and DBP increase, the proportion of people who never exercise or drink decreases, and the proportion of current smokers decreases. Baseline characteristics grouped by WC showed a similar trend. The correlations among all the indices were showed in Supplementary Table 2. The unadjusted effect size of anthropometric indices between participants with or without T2DM was showed in Supplementary Table 3. The effect size of BMI was biggest among these anthropometric indices (Cohen’s d = 0.29, 95%CI: 0.28–0.31), and BRI was smallest (Cohen’s d = 0.24, 95%CI: 0.23–0.26).

Table 1 Baseline characteristics of the included participants according to different levels of BMI

The associations of BMI and WC with T2DM are presented in Table 2. After adjusting for other covariates including age, sex, place of residence, alcohol consumption, smoking, physical exercise, SBP and RHR, in Model 3, the OR (95% CI) per SD increase in BMI was 1.287 (1.265–1.309), and compared with the first BMI quintile, the ORs (95% CIs) of the second to fifth BMI quintiles for T2DM were 1.416 (1.335–1.502), 1.664 (1.570–1.764), 1.879 (1.774–1.990) and 2.156 (2.037–2.283), respectively. The OR (95% CI) per SD increase in WC was 1.299 (1.277–1.322) in Model 3, and compared with the first WC quintile, the ORs (95% CIs) of the second to fifth WC quintiles for T2DM were 1.322 (1.244–1.404), 1.549 (1.459–1.643), 1.705 (1.609–1.807) and 2.169 (2.048–2.297), respectively.

Table 2 Association between BMI, WC and T2DM

A stratified analysis was performed by subgroups of sex in Table 3, and the results showed that a higher BMI or WC was associated with a higher risk of T2DM in both male and female.

Table 3 Association between BMI, WC and T2DM by different sex

Multivariable adjusted restricted cubic spline analysis showed the dose–response relationship between BMI, WC and T2DM in Fig. 1, and the results showed that the risk of T2DM increased with increasing BMI and WC. The associations of BMI and T2DM were nonlinear in all participants and subgroups of sex, and the association of WC and T2DM was nonlinear in the female subgroup.

Fig. 1
figure 1

Relationship of BMI and WC with the risk of T2DM for all participants and subgroups of males and females. ORs are adjusted for age, sex (not for sex subgroup analysis), alcohol consumption, place of residence, smoking, physical exercise, SBP, RHR. Abbreviations: BMI body mass index; CI confidential interval; OR odd ratio; WC waist circumference; SBP systolic blood pressure; RHR resting heart rate

The additive interaction of BMI and WC for T2DM was analyzed, and the results showed that the additive interaction did not exist (RERI: -0.059; 95% CI: -0.169 to 0.052; AP: -0.035; 95% CI: -0.100 to 0.030; S: 0.923; 95% CI: 0.797 to 1.068). As shown in Table 4, after adjusting for age, sex, place of residence, alcohol consumption, smoking, physical exercise, SBP, RHR, the AUCs of BMI, WC and other anthropometric indicators, including WHtR, BAE and BRI, for T2DM were calculated to compare the capability of those indices to identify T2DM. And the association of those anthropometric indicators with T2DM was shown in Supplementary Table 4. WHtR, BRI, BAE were positively associated with T2DM in both men and women. The ROCs are shown in Fig. 2. The best index to identify T2DM in males was WC (AUC: 0.629; 95% CI: 0.622 to 0.636), and in females, BMI (AUC: 0.600; 95% CI: 0.594 to 0.606), WC (AUC: 0.600; 95% CI: 0.593 to 0.606) and BAE (AUC: 0.600; 95% CI: 0.594 to 0.607) had a similar predictive ability for T2DM. When we adjusted for arbitrary combination of age, sex, place of residence, alcohol consumption, smoking, physical exercise, SBP and RHR (arbitrarily select 0–8 variables for adjustment), the results did not change significantly, so the findings were independent of the covariates considered.

Table 4 AUCs for anthropometric indices in relation to T2DM
Fig. 2
figure 2

The receiver operating characteristic curve of anthropometric indicators after adjusting for age, sex, alcohol consumption, place of residence, smoking, physical exercise, SBP, RHR. Abbreviations: BMI body mass index; WC waist circumference; WHtR waist-to-height ratio; BAE body adiposity estimator; BRI body roundness index; SBP systolic blood pressure; RHR resting heart rate

Discussion

Logistic regression was used in our study to examine the relationship between obesity and T2DM in the elderly, and increased BMI and WC were found to be associated with an increased risk of T2DM. The same results were found in the sex subgroup analysis. The dose–response relationship analyzed by restricted cubic splines found a nonlinear relationship between BMI and T2DM, while the relationship between WC and T2DM was nonlinear only in women. There was no additive interaction between BMI and WC for T2DM. Both BMI and WC were positively associated with T2DM. Meanwhile, we found that WC was the best predictor in elderly males, while BMI, WC and BAE had similar predictive abilities in females. When models were adjusted for arbitrary 0–8 variables of age, sex, place of residence, alcohol consumption, smoking, physical exercise, SBP and RHR, the results did not change significantly and the effect of potential confounding factors was eliminated, so the findings were independent of the covariates considered, in other words, the relationships of these anthropometric indicators with diabetes always exist no matter what covariates were adjusted in models.

Our study found that BMI and WC were positively associated with T2DM, and those positive associations were also found in some other studies [9, 24, 25]. There are several explanations for this positive association. First, people with genetic susceptibility to T2DM have a higher risk of obesity because the skeletal muscle and pancreas islet α-cells of those people are more prone to insulin resistance, and this insulin resistance leads to increased glucose production of the liver, raising insulin levels, which leads to obesity [26]. Second, macrophages in adipose tissue produce proinflammatory cytokines that influence insulin-dependent tissues and beta cells [27]. Third, the adipokine hypothesis [28] suggests that stressed adipokines release various secretory products that can affect insulin insensitivity and beta cells. Fourth, Martin G Myers Jr et al. [29] suggested that a high energy and fat diet can lead to dysfunction of the mitochondria and endoplasmic reticulum of the hypothalamus, resulting in leptin and insulin resistance. Increased leptin leads to the release of multiple inflammatory factors. Several studies have shown that some treatments for obesity, such as lifestyle changes, drug interventions, and surgery, not only lead to weight loss but also improve type 2 diabetes [30,31,32]. This also suggested that obesity increases the risk of T2DM.

In this study, the positive relationship between WC and T2DM was stronger than that of BMI in males. In contrast, the association between BMI and T2DM was stronger in females. Similar results were found by Qiwei Ge et al. [10]. This situation may be due to differences in fat distribution between the sexes [33, 34]. The study of Xuefeng Ni et al. [35] showed that women over 50 years of age had significantly less visceral abdominal fat than men, while men had more muscle mass than women. This difference in fat distribution may result in BMI becoming a better indicator of the amount of fat in women, while WC is a better indicator in men. Hormonal differences between men and women may be one reason for the difference in fat distribution [36].

In this study, ROC curves and AUC were used to compare the predictive power of BMI, WC and other anthropometric indicators, including WHtR, BAE and BRI, for T2DM. WC was the strongest predictor of T2DM in men. This result is similar to several studies [9, 24, 37]. Qiwei Ge et al. [10] also found that WC was the strongest indicator to predict T2DM in elderly men. However, these studies were not identical to the indicators of our study. In women, BMI, BAE and WC had similar predictive power for T2DM. In contrast to our study, a cohort study in Japan [38] found that BRI was better than BMI and WC in predicting T2DM in both men and women. Ye Chang et al. (20) also found that BRI had better predictive ability than BMI and WC. This discrepancy may be because the age range of the participants was different. All participants in our study were older than 60 years. We noted that the AUCs in our study were relatively low even after adjusting for some potential confounding factors, which may be because our study subjects were elderly. Qiwei Ge et al. [10] looked at people aged 18–60 and over. The AUCs of all indicators in people over 60 years old were lower than those in groups between 18 and 60 years old.

There are some advantages of our study. First, the data of this study were obtained from a large-scale health check in Henan, China. Demographic and laboratory data were collected, and the sample size and statistical power were adequate. Second, height and weight in this study were objectively measured rather than self-reported, which can avoid discrepancies between participants' own reports and the actual situation. Third, the AUCs were used to compare the predictive ability of BMI and WC with other anthropometric indicators, including WHtR, BAE and BRI, for T2DM in elderly individuals, which is of practical value to improving related studies.

However, some limitations of this study should be noted. First, the subjects of this study were older than 60 years, so we could not compare the relationship between obesity and T2DM in other age groups or the predictive ability of these indicators for diabetes. Second, this study was a cross-sectional study, making it difficult to examine the causal relationship between exposure and outcome. Third, we adjusted for potential confounders, including age, sex, alcohol consumption, smoking, physical exercise, place of residence, SBP, RHR, but some potential factors may exist that we did not adjust for, and since we did not have hip circumference information, we could not study its predictive power.

Conclusion

Overall, this study found that the increased BMI and WC were associated with an increased risk of T2DM. The same results were found in the sex subgroup analysis. There was no additive interaction between BMI and WC for T2DM. WHtR, BRI, BAE were positively associated with T2DM in both men and women. Meanwhile, we found that WC was the best predictor in older males, while BMI, WC and BAE had similar predictive abilities in females.

Availability of data and materials

The datasets generated and/or analyzed during the current study are not publicly available due to confidentiality requirements of third parties, but are available from the corresponding author on request.

Abbreviations

BMI:

Body Mass Index

WC:

Waist Circumference

T2DM:

Type 2 Diabetes Mellitus

WHtR:

Waist-to-Height Ratio

BAE:

Body Adiposity Estimator

BRI:

Body Roundness Index

AUC:

Area Under the receiver operating Characteristic Curve

OR:

Odd Ratio

CI:

Confidence Interval

CVD:

Cardiovascular Disease

ROC:

Receiver Operating Characteristic Curve

RHR:

Resting Heart Rate

SBP:

Systolic Blood Pressure

DBP:

Diastolic Blood Pressure

SD:

Standard Deviation

RERI:

Relative Excess Risk due to Interaction

AP:

Attributable Proportion due to interaction

S:

Synergy index

References

  1. Sun H, Saeedi P, Karuranga S, Pinkepank M, Ogurtsova K, Duncan BB, et al. IDF diabetes Atlas: Global, regional and country-level diabetes prevalence estimates for 2021 and projections for 2045. Diabetes Res Clin Prac. 2021;183:109119. https://doi.org/10.1016/j.diabres.2021.109119.

    Article  Google Scholar 

  2. Li Y, Teng D, Shi X, Qin G, Qin Y, Quan H, et al. Prevalence of diabetes recorded in mainland China using 2018 diagnostic criteria from the American Diabetes Association: national cross sectional study. BMJ (Clinical research ed). 2020;369: m997. https://doi.org/10.1136/bmj.m997.

    Article  Google Scholar 

  3. Harding JL, Pavkov ME, Magliano DJ, Shaw JE, Gregg EW. Global trends in diabetes complications: a review of current evidence. Diabetologia. 2019;62(1):3–16. https://doi.org/10.1007/s00125-018-4711-2.

    Article  PubMed  Google Scholar 

  4. Liu L, Chen X, Liu Y, Sun X, Yin Z, Li H, et al. The association between fasting plasma glucose and all-cause and cause-specific mortality by gender: The rural Chinese cohort study. Diabetes Metab Res Rev. 2019;35(4):e3129. https://doi.org/10.1002/dmrr.3129.

    Article  CAS  PubMed  Google Scholar 

  5. von Gunten E, Braun J, Bopp M, Keller U, Faeh D. J-shaped association between plasma glucose concentration and cardiovascular disease mortality over a follow-up of 32years. Prev Med. 2013;57(5):623–8. https://doi.org/10.1016/j.ypmed.2013.08.016.

    Article  Google Scholar 

  6. Kang N, Liu X, Liao W, Tu R, Sang S, Zhai Z, et al. Health-related quality of life among rural adults with type 2 diabetes mellitus: a cross-sectional study. Eur J Pub Health. 2021;31(3):547–53. https://doi.org/10.1093/eurpub/ckaa247.

    Article  Google Scholar 

  7. Liu M, Liu C, Zhang Z, Zhou C, Li Q, He P, et al. Quantity and variety of food groups consumption and the risk of diabetes in adults: A prospective cohort study. Clin Nutrition (Edinburgh, Scotland). 2021;40(12):5710–7. https://doi.org/10.1016/j.clnu.2021.10.003.

    Article  CAS  Google Scholar 

  8. Maddatu J, Anderson-Baucum E, Evans-Molina C. Smoking and the risk of type 2 diabetes. Translational Res : J Laboratory Clin Med. 2017;184:101–7. https://doi.org/10.1016/j.trsl.2017.02.004.

    Article  CAS  Google Scholar 

  9. Zhang FL, Ren JX, Zhang P, Jin H, Qu Y, Yu Y, et al. Strong Association of Waist Circumference (WC), Body Mass Index (BMI), Waist-to-Height Ratio (WHtR), and Waist-to-Hip Ratio (WHR) with Diabetes: A Population-Based Cross-Sectional Study in Jilin Province. China J Diabetes Res. 2021;2021:8812431. https://doi.org/10.1155/2021/8812431.

    Article  PubMed  Google Scholar 

  10. Ge Q, Li M, Xu Z, Qi Z, Zheng H, Cao Y, et al. Comparison of different obesity indices associated with type 2 diabetes mellitus among different sex and age groups in Nantong, China: a cross-section study. BMC Geriatr. 2022;22(1):20. https://doi.org/10.1186/s12877-021-02713-w.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  11. Ng M, Fleming T, Robinson M, Thomson B, Graetz N, Margono C, et al. Global, regional, and national prevalence of overweight and obesity in children and adults during 1980–2013: a systematic analysis for the Global Burden of Disease Study 2013. Lancet (London, England). 2014;384(9945):766–81. https://doi.org/10.1016/s0140-6736(14)60460-8.

    Article  Google Scholar 

  12. Zhang L, Wang Z, Wang X, Chen Z, Shao L, Tian Y, et al. Prevalence of overweight and obesity in China: Results from a cross-sectional study of 441 thousand adults, 2012–2015. Obes Res Clin Pract. 2020;14(2):119–26. https://doi.org/10.1016/j.orcp.2020.02.005.

    Article  PubMed  Google Scholar 

  13. Zhang L, Wang Z, Wang X, Chen Z, Shao L, Tian Y, et al. Prevalence of Abdominal Obesity in China: Results from a Cross-Sectional Study of Nearly Half a Million Participants. Obesity (Silver Spring, Md). 2019;27(11):1898–905. https://doi.org/10.1002/oby.22620.

    Article  Google Scholar 

  14. Calderón-García JF, Roncero-Martín R, Rico-Martín S, De Nicolás-Jiménez JM, López-Espuela F, Santano-Mogena E, et al. Effectiveness of Body Roundness Index (BRI) and a Body Shape Index (ABSI) in Predicting Hypertension: A Systematic Review and Meta-Analysis of Observational Studies. Int J Environ Res Public Health. 2021;18(21):11607. https://doi.org/10.3390/ijerph182111607.

    Article  PubMed  PubMed Central  Google Scholar 

  15. Tian S, Zhang X, Xu Y, Dong H. Feasibility of body roundness index for identifying a clustering of cardiometabolic abnormalities compared to BMI, waist circumference and other anthropometric indices: the China Health and Nutrition Survey, 2008 to 2009. Med. 2016;95(34):e4642. https://doi.org/10.1097/md.0000000000004642.

    Article  Google Scholar 

  16. Gómez-Ambrosi J, Silva C, Catalán V, Rodríguez A, Galofré JC, Escalada J, et al. Clinical usefulness of a new equation for estimating body fat. Diabetes Care. 2012;35(2):383–8. https://doi.org/10.2337/dc11-1334.

    Article  PubMed  PubMed Central  Google Scholar 

  17. Thomas DM, Bredlau C, Bosy-Westphal A, Mueller M, Shen W, Gallagher D, et al. Relationships between body roundness with body fat and visceral adipose tissue emerging from a new geometrical model. Obesity (Silver Spring, Md). 2013;21(11):2264–71. https://doi.org/10.1002/oby.20408.

    Article  Google Scholar 

  18. Weng J, Ji L, Jia W, Lu J, Zhou Z, Zou D, et al. Standards of care for type 2 diabetes in China. Diabetes Metab Res Rev. 2016;32(5):442–58. https://doi.org/10.1002/dmrr.2827.

    Article  PubMed  PubMed Central  Google Scholar 

  19. Traversy G, Chaput JP. Alcohol Consumption and Obesity: An Update. Curr Obes Rep. 2015;4(1):122–30. https://doi.org/10.1007/s13679-014-0129-4.

    Article  PubMed  PubMed Central  Google Scholar 

  20. Steiner JL, Crowell KT, Lang CH. Impact of Alcohol on Glycemic Control and Insulin Action. Biomolecules. 2015;5(4):2223–46. https://doi.org/10.3390/biom5042223.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  21. Kopelman PG. Obesity as a medical problem. Nature. 2000;404(6778):635–43. https://doi.org/10.1038/35007508.

    Article  CAS  PubMed  Google Scholar 

  22. The Joint Task Force for Guideline on the Assessment and Management of Cardiovascular Risk in China. Guideline on the assessment and management of cardiovascular risk in China. Zhonghua yu fang yi xue za zhi [Chinese journal of preventive medicine]. 2019;53(1):13–35.

    Google Scholar 

  23. Nakagawa S, Cuthill IC. Effect size, confidence interval and statistical significance: a practical guide for biologists. Biol Rev Camb Philos Soc. 2007;82(4):591–605. https://doi.org/10.1111/j.1469-185X.2007.00027.x.

    Article  PubMed  Google Scholar 

  24. Han C, Liu Y, Sun X, Luo X, Zhang L, Wang B, et al. Prediction of a new body shape index and body adiposity estimator for development of type 2 diabetes mellitus: The Rural Chinese Cohort Study. Br J Nutr. 2017;118(10):771–6. https://doi.org/10.1017/s0007114517002859.

    Article  CAS  PubMed  Google Scholar 

  25. Chang Y, Guo X, Chen Y, Guo L, Li Z, Yu S, et al. A body shape index and body roundness index: two new body indices to identify diabetes mellitus among rural populations in northeast China. BMC Public Health. 2015;15:794. https://doi.org/10.1186/s12889-015-2150-2.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  26. Malone JI, Hansen BC. Does obesity cause type 2 diabetes mellitus (T2DM)? Or is it the opposite? Pediatr Diabetes. 2019;20(1):5–9. https://doi.org/10.1111/pedi.12787.

    Article  PubMed  Google Scholar 

  27. Ortega MA, Fraile-Martínez O, Naya I, García-Honduvilla N, Álvarez-Mon M, Buján J, et al. Type 2 Diabetes Mellitus Associated with Obesity (Diabesity). The Central Role of Gut Microbiota and Its Translational Applications. Nutrients. 2020;12(9):2749. https://doi.org/10.3390/nu12092749.

    Article  PubMed Central  Google Scholar 

  28. Dyson PA. The therapeutics of lifestyle management on obesity. Diabetes Obes Metab. 2010;12(11):941–6. https://doi.org/10.1111/j.1463-1326.2010.01256.x.

    Article  CAS  PubMed  Google Scholar 

  29. Myers MG Jr, Leibel RL, Seeley RJ, Schwartz MW. Obesity and leptin resistance: distinguishing cause from effect. Trends Endocrinol Metab. 2010;21(11):643–51. https://doi.org/10.1016/j.tem.2010.08.002.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  30. Leitner DR, Frühbeck G, Yumuk V, Schindler K, Micic D, Woodward E, et al. Obesity and Type 2 Diabetes: Two Diseases with a Need for Combined Treatment Strategies - EASO Can Lead the Way. Obes Facts. 2017;10(5):483–92. https://doi.org/10.1159/000480525.

    Article  PubMed  PubMed Central  Google Scholar 

  31. Lean ME, Powrie JK, Anderson AS, Garthwaite PH. Obesity, weight loss and prognosis in type 2 diabetes. Diabet Med. 1990;7(3):228–33. https://doi.org/10.1111/j.1464-5491.1990.tb01375.x.

    Article  CAS  PubMed  Google Scholar 

  32. Williamson DF, Thompson TJ, Thun M, Flanders D, Pamuk E, Byers T. Intentional weight loss and mortality among overweight individuals with diabetes. Diabetes Care. 2000;23(10):1499–504. https://doi.org/10.2337/diacare.23.10.1499.

    Article  CAS  PubMed  Google Scholar 

  33. Mateo-Gallego R, Bea AM, Jarauta E, Perez-Ruiz MR, Civeira F. Age and sex influence the relationship between waist circumference and abdominal fat distribution measured by bioelectrical impedance. Nutrition Res (New York, NY). 2012;32(6):466–9. https://doi.org/10.1016/j.nutres.2012.05.004.

    Article  CAS  Google Scholar 

  34. Ghosh A, Bose K, Chaudhuri AB. Age and sex variations in adiposity and central fat distribution among elderly Bengalee Hindus of Calcutta. India Annals Human Biol. 2001;28(6):616–23. https://doi.org/10.1080/03014460010025167.

    Article  CAS  Google Scholar 

  35. Ni X, Jiao L, Zhang Y, Xu J, Zhang Y, Zhang X, et al. Correlation Between the Distribution of Abdominal, Pericardial and Subcutaneous Fat and Muscle and Age and Gender in a Middle-Aged and Elderly Population. Diabetes Metab Synd Obes. 2021;14:2201–8. https://doi.org/10.2147/dmso.S299171.

    Article  Google Scholar 

  36. Nedungadi TP, Clegg DJ. Sexual dimorphism in body fat distribution and risk for cardiovascular diseases. J Cardiovasc Transl Res. 2009;2(3):321–7. https://doi.org/10.1007/s12265-009-9101-1.

    Article  PubMed  Google Scholar 

  37. Motamed N, Rabiee B, Keyvani H, Hemasi GR, Khonsari M, Saeedian FS, et al. The Best Obesity Indices to Discriminate Type 2 Diabetes Mellitus. Metab Syndr Relat Disord. 2016;14(5):249–53. https://doi.org/10.1089/met.2015.0133.

    Article  CAS  PubMed  Google Scholar 

  38. Zhao W, Tong J, Li J, Cao Y. Relationship between Body Roundness Index and Risk of Type 2 Diabetes in Japanese Men and Women: A Reanalysis of a Cohort Study. Int J Endocrinol. 2021;2021:4535983. https://doi.org/10.1155/2021/4535983.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

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Acknowledgements

The investigators are grateful to the dedicated participants and all research staff of the study.

Funding

This study was supported by National Key Research and Development Program “Research on prevention and control of major chronic non-communicable diseases” of China (Grant NO: 2017YFC1307705). The funders were not involved in the study design, data collection, analysis and interpretation, and manuscript writing.

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Authors and Affiliations

Authors

Contributions

KB and XC designed the study. KB, WS conceived this article and drafted the manuscript. KB analyzed the data. SS was responsible for study concept. RS and XC made substantial contributions to the acquisition of data. All authors interpreted data, contributed to critical revisions, and had final approval of the submitted and published versions.

Corresponding author

Correspondence to Songhe Shi.

Ethics declarations

Ethics approval and consent to participate

The study was approved by the Ethics Committee of Zhengzhou University, and written informed consent was obtained from all participants (Reference Number: ZZUIRB2019-019).

All methods were performed in accordance with the relevant guidelines and regulations.

Study procedures were performed in accordance with the Declaration of Helsinki ethical principles for medical research involving human subjects.

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Not applicable.

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The authors declare that they have no competing interests.

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Supplementary Information

Additional file 1: Supplementary Figure 1.

Screening flowchart of participants. Supplementary Table 1. Baseline characteristics of the included participants according to different levels of WC. Supplementary Table 2. The Pearson correlations of all anthropometric indices. Supplementary Table 3. The effect size of anthropometric indices between groups. Supplementary Table 4. Associations between anthropometric measures and T2DM.

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Bai, K., Chen, X., Song, R. et al. Association of body mass index and waist circumference with type 2 diabetes mellitus in older adults: a cross-sectional study. BMC Geriatr 22, 489 (2022). https://doi.org/10.1186/s12877-022-03145-w

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