Skip to main content
  • Research article
  • Open access
  • Published:

Body roundness index is a superior indicator to associate with the cardio‐metabolic risk: evidence from a cross‐sectional study with 17,000 Eastern-China adults

This article has been updated

Abstract

Background

To investigate the ability of body shape index (ABSI), body roundness index (BRI), waist circumference (WC), body mass index (BMI), waist-to-hip ratio (WHR), waist-to-height ratio (WHtR), and body adiposity index (BAI) for predicting non-adipose cardio-metabolic risk.

Methods

A total of 17,360 Chinese subjects aged 18–95 years old who escaped cardiovascular disease (CVD) or diabetes were recruited in the cross-sectional study. Anthropometric and biochemical parameters were assessed. Receiver operating characteristic curve (ROC) and multinomial logistic regression were conducted to examine the association of anthropometric indicators with cardio-metabolic risk factors.

Results

The mean age of subjects were 53.7(13.1) years, 41.6 % were males. The areas under the curve (AUC) demonstrated that WC, BMI, WHR, WHtR and BRI were able to predict high cardio-metabolic risk (AUC > 0.70). Meanwhile, multinomial logistic regression showed BRI was significantly associated with high cardio-metabolic risk (OR 3.27, 95% CI 3.01–3.55). The optimal cut-off values of BRI for high cardio-metabolic risk were (< 60 y: 3.49 vs. ≥60 y: 3.46) in males and (< 60 y: 3.47 vs. ≥60 y: 3.60) in females.

Conclusions

WC, BMI WHR, and WHtR were potential obesity indicators in discriminating high cardio-metabolic risk, while BAI or ABSI was not. Moreover, BRI revealed superior predictive capacity and significant association with accumulated cardio-metabolic risk factors.

Peer Review reports

Background

Metabolic syndrome (MetSy) is a serious metabolic disorder consisting of obesity, hypertension, abnormal metabolism of lipoprotein and plasma glucose, which plays a vital role in the development of atherosclerotic heart disease, stroke and diabetes mellitus [1,2,3]. So far, over 33.9 % of older adults reached abnormal metabolism in China and caused a large disease-related healthcare burden [4,5,6,7].

MetSy was considered as an intermediate trait in the progression of severe cardiovascular disease (CVD) [8, 9] and can contribute to the risk of diabetes[10, 11]. However, obesity is an important component of metabolic syndrome that can independently contribute to the remaining components [12, 13]. Meanwhile, epidemiological studies have shown that obesity itself was a vital risk factor for hypertension [14], and cardiovascular disease [15] and diabetes [16]. Thus, that is necessary to explore the independent association between obesity and risk of CVD. Moreover, the remaining components of MetSy including hypertension, elevated fasting glucose (FPG), elevated triglycerides (TG), and reduced high-density lipoprotein cholesterol (HDL-C) were studied as the risks of CVD in previous studies [17,18,19]. Thus, the residual components of MetSy that excluding obesity were clustered as non-adipose cardio-metabolic risk factors will be more suitable for investigating the progress of cardiovascular disease or other adverse traits [4, 20]. Moreover, serum uric acid (SUA) is the end product of nucleic acid purine metabolism in body [21,22,23,24]. Previous studies revealed that an alteration of SUA level was associated with abnormal glucose and hyperuricemia, and it was considered to be a risk factor for MetSy or metabolic disorders [25,26,27].

Obesity was mainly due to the disproportionate growth of adipose tissue and lean body mass which can lead to further morbidity and mortality from cardiovascular disease [28, 29]. Recently, obesity was increasing rapidly worldwide and reached epidemic levels in China, which poses heavy public health and economic burdens [30]. The scanning of dual-energy X-ray absorptiometry (DXA), hydrostatic weighing, bioelectrical impedance and even skinfold thickness were considered as accurate methods for evaluating fat mass and distribution, whereas the use of such measurement was limited due to its complexity and/or cost [31, 32]. Epidemiological studies have revealed the anthropometric measures were acceptable indicators in evaluating obesity status for their simplicity and usefulness [20, 33,34,35]. The body mass index (BMI) has been considered as a diagnostic index for general obesity and could reflect the overall distribution of body fat [36, 37]. Meanwhile, waist circumference (WC), body adiposity index (BAI), waist-to-hip ratio (WHR) and waist-to-height ratio (WHtR) were studied to predict metabolic risk in previous studies [5, 38,39,40]. However, the traditional anthropometric indices failed to discriminate between fat and muscle mass [41, 42]. Recently, body shape index (ABSI) which reflects the body shape using waist circumference (WC), weight, and height and body roundness index (BRI) combines height and WC to predict the percentage of total and regional fat have been developed to overcome the limits of traditional obesity markers [33, 43,44,45,46,47,48,49]. A previous study found the two new indices were associated with abdominal adipose and more associated with cardiometabolic risk, onset of diabetes and premature mortality hazards than BMI and WC [4, 50, 51]. However, few shreds of evidence compared ABSI, BRI with common anthropometric indicators such as WC in the assessment of cardiometabolic risk factors in Chinese.

In this study, we clustered elevated blood pressure (BP), elevated FPG, elevated TG, reduced HDL-C and elevated serum uric acid (SUA) as non-adipose cardio-metabolic risk factors and adopted seven anthropometric indices including waist circumference (WC), body mass index (BMI), waist-to-hip ratio (WHR), waist-to-height ratio (WHtR), body adiposity index (BAI), body shape index (ABSI) and body roundness index (BRI) to conduct a population-based cross-sectional study to assess the ability of obesity indicators for predicting non-adipose cardio-metabolic risk and explore the pre-cardiovascular status in Chinese adults.

Methods

Study population

The cross-sectional data sources were the baseline records from 2009 to 2012 in Zhejiang Metabolic Syndrome Cohort (ZJMSC). ZJMSC is an ongoing community-based longitudinal study initiated in 2009 years included four communities and consisted of 22,649 participants aged 18–75 years old who have lived in Zhejiang province (Hangzhou, Zhoushan, Jiaxing, Jinhua) for more than 5 years and the follow-up visit was held from 2009 to 2019. A total of 22,649 participants (9,527 males and 13,122 females, mean age were 54.86 ± 14.2 years old) were recruited in the present study. Subjects were defined as the young group (< 60 years old) and the older group (≥ 60 years old). Exclusion criteria: (1) severe infective diseases and malignancies in baseline; (2) patients with type 2 diabetes mellitus (T2DM), cardiovascular disease (CVD) and stroke in baseline; (3) less than 18 years old; (4) without biochemical and anthropometric data. A total of 17,360 (7,226 males and 10,134 females) participants met these criteria and were finally included in this study. Additionally, inclusion criteria and selection flowchart for all samples as shown in Fig. 1. This study was approved by the Human Research Ethics Committee of Zhejiang University, Zhejiang, China. All participants provided written informed consent before participation.

Fig. 1
figure 1

Flowchart of inclusion criteria for participants in this study

Measurements

Anthropometric variables and covariates

For each participant, covariates of demographic characteristics, smoking and alcohol drinking status, diet, and physical activity was collected with questionnaire-based interview. In the present study, smoking and drinking were categorized as current, former and never. Current smokers and drinkers were defined as those who were still smoking or drinking during the investigation. Former smokers and drinkers were those who had a history of smoking or drinking and stopped for at least one year. The occupational labor strength was defined as mild labor, moderate labor, and heavy labor.

Height (cm), body weight (kg), waist circumference (WC; cm), hip circumference (HC; cm), systolic blood pressure (SBP) and diastolic blood pressure (DBP) were measured by trained assistants using medical equipment. Height and weight were measured with the subjects wearing light clothing and no shoes. Height was recorded to the nearest 0.1 cm and body weight to the nearest 0.1kg. Body mass index (BMI) was computed as weight (kg) divided by height squared (m2). The girth of the midpoint between the lowest point of the rib and the upper edge of the iliac crest were calculated as waist circumference (WC). The length of the horizontal position of the hip protrusion was calculated as the hip circumference (HC) [52]. The measurements of WC and HC were taken to the nearest 0.1 cm. Waist-to-hip ratio (WHR) and waist-to-height ratio (WHtR) were respectively calculated as WC divided by HC and WC divided by height. BAI was calculated as HC (cm)/height1.5 (m) minus 18 [53]. ABSI was calculated using the formula as \(\tt \text{ABSI}=\frac{\hbox{WC}}{{{\hbox{BMI}}^{2/3}{Height}}^{1/2}}\) and BRI was calculated using the formula as \(\hbox{BRI}=364.2-365.5\times \sqrt{1-\left(\frac{(\hbox{WC}/(2{\uppi }{\left)\right)}^{2}}{(0.5\,\hbox{Height}{)}^{2}}\right)}\). Sitting blood pressure was measured 2 times after at least 10 minutes of rest using the standardized desktop sphygmomanometer. The average blood pressure derived from two measurement readings was used [43, 51]. All variables were collected according to standard interview guidelines and standard protocols [54,55,56,57].

Biochemical measurements

After an overnight fast of at least 12 hours, intravenous blood samples of each participant were collected, with one tube for Ethylene Diamine Tetraacetic Acid (EDTA) anticoagulation and one tube for separation gel coagulation, then centrifuged at 4000 rpm for 15 min at 4℃, the aliquots were stored at − 80℃ until use. Fasting plasma glucose (FPG) was measured by the hexokinase method, SUA and lipid profile containing total cholesterol (TC), triglycerides (TG), high-density lipoprotein cholesterol (HDL-C) and low-density lipoprotein cholesterol (LDL-C) were measured by the enzymatic method using an Abbott Aeroset autoanalyzer. Alanine transaminase (ALT) and aspartate transaminase (AST) were measured with a rating method. Blood urea nitrogen was measured with uricase ultraviolet method and serum creatinine with a picric acid method.

Criteria for cardio‐metabolic risk factors

According to the diagnosis criteria of MetSy by the International Diabetes Federation (IDF) in 2009 [58], the comprehensive non-adipose cardiometabolic risk factors included the following items: (1) elevated BP: systolic blood pressure (SBP) (≥ 130 mmHg) or diastolic blood pressure (DBP) (≥ 85 mm Hg), or ongoing antihypertensive medications; (2) elevated FPG: FPG ≥ 5.6 mmol/L and/or diagnosis of type 2 diabetes, or ongoing anti-diabetic treatment; (3) elevated TG: TG ≥ 1.7 mmol/L; (4) reduced HDL-C: HDL-C < 1.03 mmol/L in men and HDL-C < 1.29 mmol/L in women. In addition, we also enrolled: (5) elevated SUA: SUA > 420µmol/L according to the diagnosis criteria of hyperuricemia in 2000 [59]. The people with three or more risks were diagnosed as “high cardio-metabolic risk population” in present study.

Statistics

The continuous variables were presented as means and standard deviations (SD), categorical variables as counts or percentages. The one-way analysis of variance and the chi-squared test were used to compare the baseline characteristics of participants stratified by the number of risk factors. The linear correlation was conducted to explore the relationship among multiple anthropometric indicators and revealed the mutative trend between median of anthropometric indicators and the number of cardiometabolic risk factors. In addition, multiple comparisons were conducted between the highest risk group and residual groups. Adjusted multinomial logistic regression was conducted to examine the associations of adiposity indicators with cardio-metabolic risk. To determine the optimal cut-off values and to compare the ability of the obesity indices for predicting multiple metabolic risk factors, the receiver operating characteristic curve (ROC) and area under the curve (AUC) were performed and optimal cut-off values were identified from the maximum Youden index (sensitivity plus specificity-1). The Hanley and McNeil method was used to compare the inter-group differences of AUCs. The analysis was performed by SPSS 25.0 software. All analyses were two-sided, and the difference was statistically significant at P < 0.05.

Results

Basic characteristics of the objects

According to the number of cardio-metabolic risk factors, subjects were divided into non-metabolic risk group, low metabolic risk group (< 3) and high metabolic risk group (≥ 3), and the differences of basic characteristics were analyzed by the presence of cardio-metabolic risk factors (Table 1). The proportion of females was higher in high metabolic risk groups (58.7 %). Participants with high cardio-metabolic risk were older than those with none or low metabolic risk (P < 0.001). In addition, participants with high cardio-metabolic risk were more likely to have higher values of SBP, DBP, FPG, TG, HDL-C, LDL-C, and SUA and lower levels of HDL-C than the other groups (P < 0.001). Moreover, participants with high cardio-metabolic risk were more likely to have higher BMI, WC, HC, WHR, WHtR, BAI, ABSI and BRI (P < 0.001). In addition, the average values of SBP, FPG and TG were abnormal in high cardio-metabolic risk group, which were 146.58 (19.23) mmHg, 5.58 (1.52) mmol/L and 2.91 (2.04) mmol/L, respectively.

Table 1 Baseline characteristics of study subjects

Cardio‐metabolic risk factors and anthropometric indicators

Table 2 shows the mean value of anthropometric parameters in multiple groups by the presence of cardio-metabolic factors. WC, BMI, WHR, WHtR, BAI, ABSI and BRI increased significantly with the number of cardio-metabolic risk factors (P_trend < 0.01). Moreover, the averages of indicators in the highest cardio-metabolic risk group were greater than residual groups (P < 0.01), and the values of WC, BMI, WHR, WHtR, BAI, ABSI and BRI were 87.25 cm, 26.68 kg/m2, 0.94, 0.54, 26.98, 0.078 and 4.23 in males, in females were 88.69 cm, 26.04 kg/m2, 0.92, 0.58, 32.31, 0.081 and 4.97. Meanwhile, the correlation matrix between anthropometric indicators was presented in Additional file 1: Table S1. In both men and women, BRI showed a strong correlation with WC (men: r = 0.93, P < 0.01; women: r = 0.94, P < 0.01) and WHtR (men: r = 0.99, P < 0.01; women: r = 0.99, P < 0.01), while the linear correlation between BRI and BMI (men: r = 0.80, P < 0.01; women: r = 0.77, P < 0.01) was relatively weak (Additional file 1: Table S1, Additional file 2: Additional Fig. S1a, b).

Table 2 The alteration of anthropometric indicators with the increase of cardiometabolic factors

AUCs of anthropometric indicators for cardio‐metabolic risk factors

Based on the result of ROC, the AUCs for each anthropometric indicator to predict multiple cardio-metabolic risk factors were presented in Additional file 1: Table S2. The AUCs presented that WC, BMI, WHR, WHtR, and BRI had better predictive ability for elevated TG in males and their AUCs were 0.70, 0.70, 0.68, 0.70 and 0.70. Similarly, the superior abilities of WC, BMI, WHR, WHtR and BRI to predict TG were observed in female, the AUCs were 0.69, 0.68, 0.67, 0.69 and 0.69. In addition, WC, WHtR and BRI displayed a superior predictive ability to high SUA in females, with AUCs of 0.69, 0.70 and 0.70, respectively. Moreover, the AUCs of obesity parameters for predicting cardio-metabolic risk factors were significant (Additional file 1: Table S2, Additional file 3: Fig. S2a–j).

Table 3 shows that WC, BMI, WHR, WHtR and BRI revealed similar abilities to predict high cardio-metabolic risk. In the young group (< 60 years), the AUCs for males were 0.74, 0.74, 0.73, 0.73, 0.73, for females were 0.73, 0.73, 0.71, 0.73 and 0.73. However, in older group (≥ 60 years), the AUCs of WC, BMI, WHR, WHtR and BRI were 0.73, 0.73, 0.70, 0.73 and 0.73 for males, and were 0.69, 0.70, 0.65, 68 and 0.68 for females. In addition, the best cut-off values of WC, BMI, WHR, WHtR and BRI were 84.45 cm, 24.04 kg/m2, 0.88, 0.51 and 3.49 in males within young group (< 60 years) and in older group (≥ 60 years), the best cut-off values were 84.75 cm, 23.24 kg/m2, 0.90, 0.51 and 3.46. Meanwhile, in females, the best cut-off values of WC, BMI, WHR, WHtR and BRI were 78.90 cm, 22.94 kg/m2, 0.85, 0.51 and 3.47 within young group (< 60 years) and were 78.85 cm, 23.73 kg/m2, 0.88, 0.51 and 3.60 in older group (≥ 60 years). Meanwhile, the sensitivity, specificity and Youden index of anthropometric measurements to predict high cardio-metabolic risk was shown in Table 3. In addition, the differences of predictive ability for high cardio-metabolic risk factors by anthropometric indicators were significant (P < 0.001) (Table 3; Fig. 2a–d).

Table 3 AUC, optimal cut-off values, sensitivity, specificity and Youden index of anthropometric indicators to predict high cardio-metabolic risk
Fig. 2
figure 2

ROC curves of anthropometric indicators to predict high cardiometabolic risk. a ROC curves in young (< 60 years old) group of males. b ROC curves in older (≥ 60 years old) group of males. c ROC curves in young (< 60 years old) group of females. d ROC curves in older (≥ 60 years old) group of females

Associations of anthropometric indicators with cardio‐metabolic risk factors

The results of logistic regression revealed that WC, BMI, WHR, WHtR and BAI, ABSI and BRI were significantly associated with accumulated cardio-metabolic risk factors in model 1 (Table 4). After adjusted covariates, the association of ABSI with high cardio-metabolic risk was suppressed (OR 1.08, 95% CI 1.01–1.16). Meanwhile, WC (OR 1.16, 95% CI 1.15–1.17), BMI (OR 1.45, 95% CI 1.41–1.47), WHR (OR 1.79, 95% CI 1.74–1.83), WHtR (OR 1.76, 95% CI 1.67–1.85) and BAI (OR 1.23, 95% CI 1.21–1.26) were associated with high accumulated cardio-metabolic risk in model 3. Moreover, BRI demonstrated the strongest relationship to accumulated cardio-metabolic risk regardless of lifestyles (OR 3.27, 95% CI 3.01–3.55).

Table 4 Association of anthropometric indicators with accumulated cardio-metabolic risk factors

Discussion

The present results indicated that WC, BMI, WHR, WHtR and BRI were able to similarly predict high cardio-metabolic risk, while BAI or ABSI was not. Moreover, BRI revealed specific predictive ability for elevated TG in the overall population and for elevated SUA in females. The superior predictive capacities and significant associations between BRI and high cardio-metabolic risk were found after adjusted covariates.

Body fat attracted intense attention when it linked with the development of cardiovascular disease and other adverse events [39, 60]. Generally, the adipose tissue concentrate in the abdomen could produce various compounds of autocrine, paracrine and endocrine activities, which could influence the metabolism and cardiovascular system [61,62,63,64]. Obesity-related indicators are non-invasive for predicting body fat mass which will become the simple and practical adiposity markers[65]. The traditional indicators of WC, BMI, WHR, WHtR and BAI were widely recruited to explore the association of adiposity with metabolic disorder, cardiovascular morbidity and diabetes, but the results were unclear due to the delusive relationship with fat mass and distribution [44, 66,67,68]. Meanwhile, ABSI and BRI were considered as effective indicators for predicting obesity status and risk of metabolic syndrome [51, 69]. A previous study examined the predictive capacity of ABSI and BRI to identify hyperuricemia and to compare the relative strength of association between anthropometric indices and hyperuricemia in rural China [51]. The results found BRI (AUC: 0.641; OR: 1.459) showed more powerful predictive ability for hyperuricemia than BMI (AUC: 0.630; OR: 1.108), while having a similar predictive power as WHtR (AUC: 0.656; OR:1.067) and WC (AUC: 0.658; OR: 1.047) in the female group, but not in the male group. However, ABSI had the lowest predictive power for hyperuricemia in both sex categories. Based on the large-scale population, the similar results were stably validated in our study and the predictive AUC for hyperuricemia was 0.70 in females. For the predictive capacity and association to cardiometabolic risk factors, BRI could be used as an alternative body index to WHtR, while ABSI could not. Meanwhile, a study with Polish population also showed that BRI had superior ability to predict metabolic syndrome [46]. Generally, BRI possesses a stable ability to predict cardiometabolic risk and metabolic syndrome even in different ethnic groups, and these results were well determined in our study [49]. Moreover, Chang et al. [64]. found that BRI (AUC = 0.74), not ABSI was superior measurement compared to BMI, WC and WHtR for determining the presence of left ventricular hypertrophy, especially for eccentric left ventricular hypertrophy [50]. Obesity was supposed to increase fat accumulation in the cardiac which is associated with ventricular hypertrophy and ventricular systolic dysfunction [70]. Body roundness index (BRI) was developed to predict both body fat and the percentage of visceral adipose tissue using WC in relation to height, which will estimate the shape of the human body figure as an ellipse [4, 43, 71]. BRI was generally used as an adipose indicator for determining the presence of hyperuricemia, arterial stiffness, CVD, diabetes, dyslipidemia, hypertension, and MetSy [7, 46, 49, 51, 67, 68]. However, BRI was limited in predicting percentage of fat mass in athletes when compared with bio-impedance analysis or skinfold prediction [72]. Although BRI was not superior to WHtR for determining the presence of MetSy or cardio-metabolic risk, there were no significant differences in predicting MetS, suggesting that BRI was an alternative obesity indicator [43, 73]. The advantages of BRI exceed BMI and WHR were commonly believed to improve the predictive power of body fat and visceral adipose tissue and visceral adipose tissue was associated with MetSy was well known [46, 50, 74].

The present study included the large sample size and involved multi-regional population, which avoided the shortcomings of many previous studies. We confirmed BRI was superior indicator for multiple cardio-metabolic risk factors in Chinese adults. Meanwhile, a cross-sectional study also revealed only BRI, not ABSI, can determine the presence of MetSy and insulin resistance (IR) in the overweight and obesity population [75]. Although many advantages were presented, the limitations should be considered in our study. The numerous obesity indicators were included to predict the cardio-metabolic risk, but the roles of different obesity indicators in presenting fat mass were unique. BMI presented fat mass in the whole body, while WHR was generally regarded as the index in abdominal fat. The obesity indicators were initially conducted to research the associations with cardiovascular disease and mortality in developed countries. We recruited the experienced indicators to predict cardio-metabolic risk in Chinese adults, which may be the main reason why the ABSI failed to predict cardio-metabolic risk. In addition, the study was conducted with rural populations residing in southeast China, the unique lifestyle may influence the body shape and metabolic indices. Third, although BRI improved quantification of body shape and provided a more accurate estimate of adipose tissue, the calculation of BRI was so complicated that influenced the clinical application. The longitudinal relationship between BRI and cardio-metabolic risk should be examined in future, meanwhile the multi-centers and minority studies are needed to identify the association of obesity indices with more comprehensive metabolic risk factors.

Conclusions

The present study indicated BRI, WC, BMI, WHR, and WHtR were likely to be optimal indicators for determining the presence of cardio-metabolic risk, especially for high cardio-metabolic risk. BRI was superior and alternative indicator for predicting accumulated cardio-metabolic risk in Chinese adults.

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Change history

  • 24 February 2021

    In the original article 12872_2021_1905_MOESM3_ESM.jpg was missing. An amendment to this paper has been published and can be accessed via the original article.

Abbreviations

ROC:

Receiver operating characteristic curve

AUC:

Areas under the curve

CVD:

Cardiovascular disease

T2DM:

Type 2 diabetes mellitus

EDTA:

Ethylene diamine tetraacetic acid

MetSy:

Metabolic syndrome

WC:

Waist circumference

HC:

Hip circumference

BMI:

Body mass index

WHR:

Waist-to-hip ratio

WHtR:

Waist-to-height ratio

BAI:

Body adiposity index

ABSI:

A body shape index

BRI:

Body roundness index

SBP:

Systolic blood pressure

DBP:

Diastolic blood pressure

FPG:

Fasting plasma glucose

TG:

Triglyceride

HDL-C:

High-density lipoprotein cholesterol

LDL-C:

Low-density lipoprotein cholesterol

SUA:

Serum uric acid

BP:

Blood press

ALT:

Alanine transaminase

AST:

Sspartate transaminase

References

  1. Saklayen MG. The global epidemic of the metabolic syndrome. Curr Hypertens Rep. 2018;20:2.

    Article  Google Scholar 

  2. Akinyemiju T, Moore J, Pisu M, Judd S, Goodman M, Shikany J, et al. A prospective study of obesity, metabolic health, and cancer mortality. Obesity. 2018;26:1.

    Article  Google Scholar 

  3. Kachur S, Morera R, De AS, Lavie CJ. Cardiovascular risk in patients with prehypertension and the metabolic syndrome. Curr Hypertens Rep. 2018;20:2.

    Article  Google Scholar 

  4. Gu Z, Li D, He H, Wang J, Hu X, Zhang P, et al. Body mass index, waist circumference, and waist-to-height ratio for prediction of multiple metabolic risk factors in Chinese elderly population. Sci Rep. 2018;8:1.

    Article  Google Scholar 

  5. Jiang CQ, Xu L, Zhang WS, Jin YL, Zhu F, Cheng KK, et al. Adiposity and mortality in older Chinese: an 11-year follow-up of the Guangzhou Biobank Cohort Study. Sci Rep. 2020;10:1.

    CAS  Google Scholar 

  6. Li W, Song F, Wang X, Wang D, Lu Z. Relationship between metabolic syndrome and its components and cardiovascular disease in middle-aged and elderly Chinese population: a national cross-sectional survey. BMJ Open. 2019;9:8.

    Article  Google Scholar 

  7. Liu PJ, Ma F, Lou HP, Zhu YN. Comparison of the ability to identify cardiometabolic risk factors between two new body indices and waist-to-height ratio among Chinese adults with normal BMI and waist circumference. Public Health Nutr. 2017;20:6.

    Article  Google Scholar 

  8. Martinelli I, Tomassoni D, Moruzzi M, Roy P, Cifani C, Amenta F, et al. Cardiovascular changes related to metabolic syndrome: evidence in obese zucker rats. Int J Mol Sci. 2020;21:6.

    Article  Google Scholar 

  9. Stehouwer CD, Henry RM, Ferreira I. Arterial stiffness in diabetes and the metabolic syndrome: a pathway to cardiovascular disease. Diabetologia. 2008;51:4.

    Article  Google Scholar 

  10. Hanley AJ, Karter AJ, Williams K, Festa A, D’Agostino RB Jr, Wagenknecht LE, et al. Prediction of type 2 diabetes mellitus with alternative definitions of the metabolic syndrome: the Insulin Resistance Atherosclerosis Study. Circulation. 2005;112:24.

    Article  Google Scholar 

  11. Salzano A, D’Assante R, Heaney LM, Monaco F, Rengo G, Valente P, et al. Klinefelter syndrome, insulin resistance, metabolic syndrome, and diabetes: review of literature and clinical perspectives. Endocrine. 2018;61:2.

    Article  Google Scholar 

  12. Sanghera DK, Bejar C, Sharma S, Gupta R, Blackett PR. Obesity genetics and cardiometabolic health: potential for risk prediction. Diabetes Obes Metab. 2019;21:5.

    Article  Google Scholar 

  13. Iyer A, Fairlie DP, Prins JB, Hammock BD, Brown L. Inflammatory lipid mediators in adipocyte function and obesity. Nat Rev Endocrinol. 2010;6:2.

    Article  Google Scholar 

  14. Susic D, Varagic J, Obesity. A perspective from hypertension. Med Clin N Am. 2017;101:1.

    Google Scholar 

  15. Ortega FB, Lavie CJ, Blair SN. Obesity and cardiovascular disease. Circ Res. 2016;118:11.

    Article  Google Scholar 

  16. Liu LL, Lawrence JM, Davis C, Liese AD, Pettitt DJ, Pihoker C, et al. Prevalence of overweight and obesity in youth with diabetes in USA: the SEARCH for Diabetes in Youth study. Pediatr Diabetes. 2010;11:1.

    Article  Google Scholar 

  17. Henderson DC, Vincenzi B, Andrea NV, Ulloa M, Copeland PM. Pathophysiological mechanisms of increased cardiometabolic risk in people with schizophrenia and other severe mental illnesses. Lancet Psychiatry. 2015;2:5.

    Article  Google Scholar 

  18. Pope CA, Turner MC, Burnett RT, Jerrett M, Gapstur SM, Diver WR, et al. Relationships between fine particulate air pollution, cardiometabolic disorders, and cardiovascular mortality. Circ Res. 2015;116:1.

    Article  Google Scholar 

  19. Haghikia A, Landmesser U. Lipoproteins and cardiovascular redox signaling: role in atherosclerosis and coronary disease. Antioxid Redox Signal. 2018;29:3.

    Article  Google Scholar 

  20. Kahn HS, Divers J, Fino NF, Dabelea D, Bell R, Liu LL, et al. Alternative waist-to-height ratios associated with risk biomarkers in youth with diabetes: comparative models in the SEARCH for Diabetes in Youth Study. Int J Obes (Lond). 2019;43:10.

    Article  Google Scholar 

  21. Kallistratos M, Giannitsi S, Poulimenos L, Miaris N, Koukouzeli A, Khashlok LA, et al. Uric acid as a risk factor for cardiovascular disease. A prospective observational study. J Hypertens. 2018;36:3.

    Google Scholar 

  22. Borghi C, Rodriguez-Artalejo F, De Backer G, Dallongeville J, Medina J, Nuevo J, et al. Serum uric acid levels are associated with cardiovascular risk score: a post hoc analysis of the EURIKA study. Int J Cardiol. 2018;253:1.

    Article  Google Scholar 

  23. Borghi C, Rosei EA, Bardin T, Dawson J, Dominiczak A, Kielstein JT, et al. Serum uric acid and the risk of cardiovascular and renal disease. J Hypertens. 2015;33:9.

    Article  Google Scholar 

  24. Kuwabara M, Hisatome I, Niwa K, Hara S, Roncal-Jimenez CA, Bjornstad P, et al. Uric acid is a strong risk marker for developing hypertension from prehypertension: a 5-year Japanese cohort study. Hypertension. 2018;71:1.

    Article  Google Scholar 

  25. Li Q, Zhang Y, Ding D, Yang Y, Chen Q, Liu C, et al. Association between serum uric acid and mortality among Chinese patients with coronary artery disease. Cardiology. 2016;134:3.

    Article  Google Scholar 

  26. Song M, Li N, Yao Y, Wang K, Yang J, Cui Q, et al. Longitudinal association between serum uric acid levels and multiterritorial atherosclerosis. J Cell Mol Med. 2019;23:8.

    Article  Google Scholar 

  27. Wu L, He Y, Jiang B, Liu M, Wang J, Zhang D, et al. Association between serum uric acid level and hypertension in a Chinese elderly rural population. Clin Exp Hypertens. 2017;39:6.

    Article  Google Scholar 

  28. Matthias B. Obesity: global epidemiology and pathogenesis. Nat Rev Endocrinol. 2019;12:6.

    Google Scholar 

  29. Piché M-E, Tchernof A, Després J-P. Obesity phenotypes, diabetes, and cardiovascular diseases. Circ Res. 2020;126:11.

    Article  Google Scholar 

  30. Lu J, Wang L, Li M, Xu Y, Ning G. Metabolic syndrome among adults in China: the 2010 China Noncommunicable Disease Surveillance. J Clin Endocrinol Metab. 2016;102:2.

    Google Scholar 

  31. DR AG, JO T, AM C, MA G, TJ S, et al. The effect of adiposity measured by dual-energy X-ray absorptiometry on lung function. Eur Respir J. 2008;32:1.

    Google Scholar 

  32. Britton KA, Massaro JM, Murabito JM, Kreger BE, Hoffmann U, Fox CS. Body fat distribution, incident cardiovascular disease, cancer, and all-cause mortality. J Am Coll Cardiol. 2013;62:10.

    Article  Google Scholar 

  33. Zhao Q, Zhang K, Li Y, Zhen Q, Shi J, Yu Y, et al. Capacity of a body shape index and body roundness index to identify diabetes mellitus in Han Chinese people in Northeast China: a cross-sectional study. Diabetes Med. 2018;35:11.

    Article  Google Scholar 

  34. Xing Z, Tang L, Chen J, Pei J, Chen P, Fang Z, et al. Association of predicted lean body mass and fat mass with cardiovascular events in patients with type 2 diabetes mellitus. Cmaj. 2019;191:38.

    Article  Google Scholar 

  35. Xing Z, Peng Z, Wang X, Zhu Z, Pei J, Hu X, et al. Waist circumference is associated with major adverse cardiovascular events in male but not female patients with type-2 diabetes mellitus. Cardiovasc Diabetol. 2020;19:1.

    Article  Google Scholar 

  36. Aguilar-Morales I, Colin-Ramirez E, Rivera-Mancia S, Vallejo M, Vazquez-Antona C. Performance of waist-to-height ratio, waist circumference, and body mass index in discriminating cardio-metabolic risk factors in a sample of school-aged Mexican children. Nutrients. 2018;10:12.

    Article  Google Scholar 

  37. Elagizi A, Kachur S, Lavie CJ, Carbone S, Pandey A, Ortega FB, et al. An overview and update on obesity and the obesity paradox in cardiovascular diseases. Prog Cardiovasc Dis. 2018;61:2.

    Article  Google Scholar 

  38. Hsieh SD, Muto T, Tsuji H, Arase Y, Murase T. Clustering of other metabolic risk factors in subjects with metabolic syndrome. Metabolism. 2010;59:5.

    Article  Google Scholar 

  39. Jenkins DA, Bowden J, Robinson HA, Sattar N, Loos RJF, Rutter MK, et al. Adiposity-mortality relationships in type 2 diabetes, coronary heart disease, and cancer subgroups in the UK Biobank, and their modification by smoking. Diabetes Care. 2018;41:9.

    Article  Google Scholar 

  40. Moliner-Urdiales D, Artero EG, Lee DC, Espana-Romero V, Sui X, Blair SN. Body adiposity index and all-cause and cardiovascular disease mortality in men. Obesity (Silver Spring). 2013;21:9.

    Article  Google Scholar 

  41. Myint PK, Kwok CS, Luben RN, Wareham NJ, Khaw KT. Body fat percentage, body mass index and waist-to-hip ratio as predictors of mortality and cardiovascular disease. Heart. 2014;100:20.

    Article  Google Scholar 

  42. Quadros TMB, Gordia AP, Andaki ACR, Mendes EL, Mota J, Silva LR. Utility of anthropometric indicators to screen for clustered cardiometabolic risk factors in children and adolescents. J Pediatr Endocrinol Metab. 2019;32:1.

    Article  Google Scholar 

  43. Geraci G, Zammuto M, Gaetani R, Mattina A, D’Ignoto F, Geraci C, et al. Relationship of a Body Shape Index and Body Roundness Index with carotid atherosclerosis in arterial hypertension. Nutr Metab Cardiovasc Dis. 2019;29:8.

    Article  Google Scholar 

  44. Khader Y, Batieha A, Jaddou H, El-Khateeb M, Ajlouni K. The performance of anthropometric measures to predict diabetes mellitus and hypertension among adults in Jordan. BMC Public Health. 2019;19:1.

    Article  Google Scholar 

  45. Li G, Wu HK, Wu XW, Cao Z, Tu YC, Ma Y, et al. The feasibility of two anthropometric indices to identify metabolic syndrome, insulin resistance and inflammatory factors in obese and overweight adults. Nutrition. 2019;57:1.

    Article  Google Scholar 

  46. Suliga E, Ciesla E, Gluszek-Osuch M, Rogula T, Gluszek S, Koziel D. The usefulness of anthropometric indices to identify the risk of metabolic syndrome. Nutrients. 2019;11:11.

    Article  Google Scholar 

  47. Christakoudi S, Tsilidis KK, Muller DC, Freisling H, Weiderpass E, Overvad K, et al. A Body Shape Index (ABSI) achieves better mortality risk stratification than alternative indices of abdominal obesity: results from a large European cohort. Sci Rep. 2020;10:1.

    Article  Google Scholar 

  48. Li G, Yao T, Wu XW, Cao Z, Tu YC, Ma Y, et al. Novel and traditional anthropometric indices for identifying arterial stiffness in overweight and obese adults. Clin Nutr. 2020;39:3.

    Article  Google Scholar 

  49. Rico-Martin S, Calderon-Garcia JF, Sanchez-Rey P, Franco-Antonio C, Martinez Alvarez M, Sanchez Munoz-Torrero JF. Effectiveness of body roundness index in predicting metabolic syndrome: a systematic review and meta-analysis. Obes Rev. 2020;21:7.

    Article  Google Scholar 

  50. Chang Y, Guo X, Li T, Li S, Guo J, Sun Y. A Body Shape Index and Body Roundness Index: two new body indices to identify left ventricular hypertrophy among rural populations in Northeast China. Heart Lung Circ. 2016;25:4.

    Article  Google Scholar 

  51. Zhang N, Chang Y, Guo X, Chen Y, Ye N, Sun Y. A Body Shape Index and Body Roundness Index: Two new body indices for detecting association between obesity and hyperuricemia in rural area of China. Eur J Intern Med. 2016;29:1.

    Article  Google Scholar 

  52. Caminha TCS, Ferreira HS, Costa NS, Nakano RP, Assunção ML. Waist-to-height ratio is the best anthropometric predictor of hypertension: a population-based study with women from a state of northeast of Brazil. Medicine. 2017;96:2.

    Article  Google Scholar 

  53. Fedewa MV, Nickerson BS, Esco MR. Associations of body adiposity index, waist circumference, and body mass index in young adults. Clin Nutr. 2018;1:6.

    Google Scholar 

  54. Li J, Li J, Wang H, Qi L-W, Zhu Y, Lai M. Tyrosine and glutamine-leucine are metabolic markers of early-stage colorectal cancers. Gastroenterology. 2019;157:1.

    Article  Google Scholar 

  55. Ruizhi Z, Chengguo L, Chunmei W, Biao Z, Yi L, Feixia P, et al. Natural course of metabolically healthy overweight/obese subjects and the impact of weight change. Nutrients. 2016;8:7.

    Google Scholar 

  56. Yimin Z, Dandan Z, Dan Z, Zhenli L, Zhiqiang L, Le F, et al. Susceptibility loci for metabolic syndrome and metabolic components identified in Han Chinese: a multi-stage genome-wide association study. J Cell Mol Med. 2017;21:6.

    Google Scholar 

  57. Zheng Q, Lin W, Liu C, Zhou Y, Chen T, Zhang L, et al. Prevalence and epidemiological determinants of metabolically obese but normal-weight in Chinese population. BMC Public Health. 2020;20:1.

    Article  Google Scholar 

  58. Alberti KGMM, Zimmet P, Shaw J. Metabolic syndrome—a new world-wide definition. A Consensus Statement from the International Diabetes Federation. Diabetes Med. 2006;23:5.

    Article  Google Scholar 

  59. Khichar S, Choudhary S, Singh VB, Tater P, Ujjawal V. Serum uric acid level as a determinant of the metabolic syndrome: a case control study. Diabetes Metab Syndrome Clin Res Rev. 2016;11:1.

    Google Scholar 

  60. Kannel WB, Cupples LA, Ramaswami R, Stokes J 3rd, Kreger BE, Higgins M. Regional obesity and risk of cardiovascular disease; the Framingham Study. J Clin Epidemiol. 1991;44:2.

    Article  Google Scholar 

  61. Lee JJ, Pedley A, Hoffmann U, Massaro JM, Levy D, Long MT. Visceral and intrahepatic fat are associated with cardiometabolic risk factors above other ectopic fat depots: the Framingham Heart Study. Am J Med. 2018;131:6.

    Article  Google Scholar 

  62. Kim Y, Wijndaele K, Lee DC, Sharp SJ, Wareham N, Brage S. Independent and joint associations of grip strength and adiposity with all-cause and cardiovascular disease mortality in 403,199 adults: the UK Biobank study. Am J Clin Nutr. 2017;106:3.

    Google Scholar 

  63. Hamer M, Stamatakis E. Metabolically healthy obesity and risk of all-cause and cardiovascular disease mortality. J Clin Endocrinol Metab. 2012;97:7.

    Article  Google Scholar 

  64. Moliner-Urdiales D, Artero EG, Lee DC, Espana-Romero V, Sui X, Blair SN. Body adiposity index and all-cause and cardiovascular disease mortality in men. Obesity. 2013;21:9.

    Article  Google Scholar 

  65. L CC DVF. E UR, A KJ. Anthropometric indicators as predictors of total body fat and cardiometabolic risk factors in Chilean children at 4, 7 and 10 years of age. Eur J Clin Nutr. 2017;71:4.

    Google Scholar 

  66. Borel AL, Coumes S, Reche F, Ruckly S, Pépin JL, Tamisier R, et al. Waist, neck circumferences, waist-to-hip ratio: which is the best cardiometabolic risk marker in women with severe obesity? The SOON cohort. PLoS One. 2018;13:11.

    Article  Google Scholar 

  67. Mohan V, Sandeep S, Deepa M, Gokulakrishnan K, Datta M, Deepa R. A diabetes risk score helps identify metabolic syndrome and cardiovascular risk in Indians—the Chennai Urban Rural Epidemiology Study (CURES-38). Diabetes Obes Metab. 2007;9:3.

    Article  Google Scholar 

  68. Rådholm K, Chalmers J, Ohkuma T, Peters S, Poulter N, Hamet P, et al. Use of the waist-to-height ratio to predict cardiovascular risk in patients with diabetes: results from the ADVANCE-ON study. Diabetes Obes Metab. 2018;20:8.

    Article  Google Scholar 

  69. Bertoli S, Leone A, Krakauer NY, Bedogni G, Battezzati A. Association of Body Shape Index (ABSI) with cardio-metabolic risk factors: a cross-sectional study of 6081 Caucasian adults. Plos One. 2017;12:9.

    Article  Google Scholar 

  70. BP L, AB DC, C R, AE GB. Effect of obesity on left ventricular mass and systolic function in patients with asymptomatic aortic stenosis (a Simvastatin Ezetimibe in Aortic Stenosis (SEAS) substudy). Am J Cardiol. 2010;105:10.

    Google Scholar 

  71. Ibiza A-M, Eloisa C-R, Susana R-M, Maite V, Clara V-A. Performance of waist-to-height ratio, waist circumference, and Body Mass Index in discriminating cardio-metabolic risk factors in a sample of school-aged Mexican children. Nutrients. 2018;10:12.

    Google Scholar 

  72. A SD, M SA. N MC, P MJ, S MC, M TD, et al. Utility of novel body indices in predicting fat mass in elite athletes. Nutrition. 2015;31:7–8.

    Google Scholar 

  73. Bertoli S, Leone A, Krakauer NY, Bedogni G, Vanzulli A, Redaelli VI, et al. Association of Body Shape Index (ABSI) with cardio-metabolic risk factors: a cross-sectional study of 6081 Caucasian adults. PLoS One. 2017;12:9.

    Article  Google Scholar 

  74. Jing D, Si-Si W, Xi C, et al. Optimal cut-off point of waist to height ratio in Beijing and its association with clusters of metabolic risk factors. Curr Med Sci. 2019;39:2.

    Google Scholar 

  75. Gang L, Hui-Kun W, Xiao-Wei W, Zhe C, Yuan-Chao T, Yi M, et al. The feasibility of two anthropometric indices to identify metabolic syndrome, insulin resistance and inflammatory factors in obese and overweight adults. Nutrition. 2019;57:1.

    Google Scholar 

Download references

Acknowledgements

Not applicable.

Funding

This work was supported by the grants from National Key Research and Development Program of China (2017YFC0907004) and Hangzhou Science and Technology Project (20171226Y27). The funding agencies had no role in the study design, data collection and analysis, decision to publish or preparation of the manuscript.

Author information

Authors and Affiliations

Authors

Contributions

JJX designed the work and drafted the manuscript; LQZ and QW revised the manuscript critically for important intellectual content; YHZ and ZQJ collected and interpreted the data; ZJL created new software used in the work; YMZ were the designer of the manuscript and approved to submit the manuscript finally. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Yimin Zhu.

Ethics declarations

Ethical approval and consent to participate

Informed and written consent was obtained from all participants, and the protocol was approved by the Zhejiang University ethics committee. The study was conducted according to the ethical guidelines of the Helsinki Declaration and Chinese legislation regarding the protection of personal data was also followed.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Additional file 1: Table S1

. The correlation matrix for multiple anthropometric indicators. WC waist circumference; HC hip circumference; BMI body mass index; WHR waist-to-hip ratio; WHtR waist-to-height ratio; BAI body adiposity index; ABSI a body shape index; BRI body roundness index, *P value < 0.01. Table S2. Area under curves (95% CI) of anthropometric indicators to predict cardio-metabolic risk factors. **P value < 0.001, the inter-group difference of AUCs under the ROC curve; WC waist circumference; HC hip circumference; BMI body mass index; WHR waist-to-hip ratio; WHtR waist-to-height ratio; BAI body adiposity index; ABSI a body shape index; BRI body roundness index, BP blood pressure; FPG fasting plasma glucose; TG triglyceride; HDL-C high-density lipoprotein cholesterol; SUA serum uric acid.

Additional file 2: Figure S1

. Heatmap of the correlation between anthropometric indicators. (a) The correlation matrix between anthropometric indicators in males; (b) The correlation matrix between anthropometric indicators in females; WC waist circumference; HC hip circumference; BMI body mass index; WHR waist-to-hip ratio; WHtR waist-to-height ratio; BAI body adiposity index; ABSI a body shape index; BRI body roundness index.

Additional file 3: Figure S2

. ROC curves of anthropometric indicators to predict multiple cardiometabolic risk factors. (a) ROC curves of anthropometric indicators to predict elevated BP in male; (b) ROC curves of anthropometric indicators to predict elevated FPG in male; (c) ROC curves of anthropometric indicators to predict elevated TG in male; (d) ROC curves of anthropometric indicators to predict reduced HDL-C in male; (e) ROC curves of anthropometric indicators to predict elevated SUA in male; (f) ROC curves of anthropometric indicators to predict elevated BP in female; (g) ROC curves of anthropometric indicators to predict elevated FPG in female; (h) ROC curves of anthropometric indicators to predict elevated TG in female; (i) ROC curves of anthropometric indicators to predict reduced HDL-C in female; (j) ROC curves of anthropometric indicators to predict elevated SUA in female; WC waist circumference; HC hip circumference; BMI body mass index; WHR waist-to-hip ratio; WHtR waist-to-height ratio; BAI body adiposity index; ABSI a body shape index; BRI body roundness index, BP blood pressure; FPG fasting plasma glucose; TG triglyceride; HDL-C high-density lipoprotein cholesterol; SUA serum uric acid.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Xu, J., Zhang, L., Wu, Q. et al. Body roundness index is a superior indicator to associate with the cardio‐metabolic risk: evidence from a cross‐sectional study with 17,000 Eastern-China adults. BMC Cardiovasc Disord 21, 97 (2021). https://doi.org/10.1186/s12872-021-01905-x

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12872-021-01905-x

Keywords