# Associations between a body shape index and coronary heart disease: a case–control study in southern China

**Authors:** Weikun Zhao, Ruiyan Huang, Renxuan Qin, Xinlong Zhang, Jinquan Zeng, Feng Huang, Rongjie Huang

PMC · DOI: 10.3389/fcvm.2026.1698541 · Frontiers in Cardiovascular Medicine · 2026-02-04

## TL;DR

This study finds that a body shape index (ABSI) is a useful predictor of coronary heart disease risk in southern China when combined with other factors.

## Contribution

The study introduces ABSI as a novel predictor of CHD risk in the southern Chinese population, improving predictive models when combined with other variables.

## Key findings

- ABSI was among the most influential predictors of CHD risk in southern Chinese patients.
- A multivariable model incorporating ABSI and other factors achieved an AUC of 0.809 for CHD prediction.
- The developed nomogram provides a quantitative tool for individualized CHD risk estimation.

## Abstract

Coronary heart disease (CHD) burden is increasing, and traditional obesity measures inadequately capture fat distribution and associated CHD risk. A body shape index (ABSI) is an emerging anthropometric metric of fat distribution, but evidence linking ABSI to CHD is limited, particularly in the Chinese population. This case-control study in southern China investigated the association of ABSI and related factors with CHD risk, aiming to facilitate early identification of high-risk individuals.

We retrospectively studied 996 patients who underwent coronary angiography in a southern Chinese hospital. After strict screening and propensity score matching (PSM), 125 patients with CHD (>50% coronary stenosis) and 125 controls (<50% stenosis) were selected. Key CHD risk predictors were identified using feature-selection techniques (LASSO regression, recursive feature elimination, random forest importance). Univariate and multivariate logistic regression models were constructed for CHD prediction. Model performance was evaluated by receiver operating characteristic (ROC) analysis and compared to individual predictors using the DeLong test. A nomogram was developed for individualized risk estimation.

Baseline characteristics were well matched between CHD and control groups after PSM. Across feature-selection methods, the most influential predictors for CHD included ABSI, prealbumin (PA), direct-to-total bilirubin ratio (DB/TB), apolipoprotein B (ApoB), globulin (GLO), apolipoprotein A-I (ApoA-I), and essential hypertension (EH). Each of these factors showed a significant univariate association with CHD (P < 0.05) but only modest predictive power individually (AUCs 0.57–0.66). ABSI exhibited the highest sensitivity (86.4%) among single predictors, while ApoB had the highest specificity (78.4%). The multivariable logistic model incorporating these variables achieved an AUC of 0.809, significantly outperforming any individual predictor (P < 0.001). At the optimal probability cutoff, the model's sensitivity and specificity were 69.6% and 82.4%, respectively. The nomogram combined ABSI with other key variables to provide a quantitative CHD risk estimate for individual patients.

This study identifies ABSI as a potential predictor of CHD risk among southern Chinese populations. Integrating ABSI with other candidate predictors improves the model's predictive performance. A multifactorial approach may better characterize CHD risk in this population and could inform prevention strategies.

## Linked entities

- **Diseases:** coronary heart disease (MONDO:0005010), essential hypertension (MONDO:0001134)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, APOA1 (apolipoprotein A1) [NCBI Gene 335] {aka AMYLD3, HPALP2, apo(a)}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, APOB (apolipoprotein B) [NCBI Gene 338] {aka FCHL2, FLDB, LDLCQ4, apoB-100, apoB-48}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}
- **Diseases:** ABSI (MESH:C566784), AS (MESH:D050197), death (MESH:D003643), Hypertension (MESH:D006973), ischemic heart disease (MESH:D017202), cardiovascular conditions (MESH:D002318), acute myocardial infarction (MESH:D009203), insulin resistance (MESH:D007333), adiposity (MESH:D018205), heart failure (MESH:D006333), heart disease (MESH:D006331), abnormal liver function (MESH:D056486), Central obesity (MESH:D056128), metabolic syndrome (MESH:D024821), inflammation (MESH:D007249), liver diseases (MESH:D008107), CHD (MESH:D003327), dyslipidemia (MESH:D050171), double-vessel disease (MESH:C536223), DM (MESH:D003920), NAFLD (MESH:D065626), obese (MESH:D009765), EH (MESH:D000075222), stenotic lesions (MESH:D009059), stroke (MESH:D020521), triple-vessel disease (MESH:C536008), single-vessel disease (MESH:D012640), stenosis (MESH:D003251), coronary stenosis (MESH:D023921)
- **Chemicals:** A1c (-), urea nitrogen (MESH:C530477), lipid (MESH:D008055), creatinine (MESH:D003404), glucose (MESH:D005947), Bilirubin (MESH:D001663), TG (MESH:D014280), TB (MESH:D013725), free fatty acids (MESH:D005230), Blood glucose (MESH:D001786), cholesterol (MESH:D002784)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12913546/full.md

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Source: https://tomesphere.com/paper/PMC12913546