# Association Between Waist Circumference and Coronary Artery Disease: Evidence from the NHANES 1999–2023 Cross-Sectional Data and Mendelian Randomization Analysis

**Authors:** Liheng Chen, Qian Shang, Yu Li

PMC · DOI: 10.5334/gh.1529 · Global Heart · 2026-02-26

## TL;DR

This study shows that higher waist circumference causes an increased risk of coronary artery disease, using both observational and genetic evidence.

## Contribution

The study provides novel causal evidence for the role of waist circumference in CAD using Mendelian randomization and NHANES data.

## Key findings

- WC was significantly higher in CAD patients compared to controls (p < 0.001).
- MR analysis confirmed a causal link between WC and CAD (p = 0.00000883).
- Sensitivity tests supported the robustness of the causal relationship.

## Abstract

Central obesity, as indicated by waist circumference (WC), is a major risk factor for coronary artery disease (CAD). However, the independent causal role of WC in CAD remains underexplored, particularly after adjusting for metabolic comorbidities such as hypertension and diabetes.

This study aims to evaluate the causal relationship between WC and CAD using a two-pronged approach: propensity score-matched observational analysis and Mendelian randomization (MR) analysis.

Data from the National Health and Nutrition Examination Survey (NHANES) 1999–2023 were used for cross-sectional analysis, while genetic instrumental variables associated with WC were sourced from genome-wide association studies (GWAS). We performed inverse variance weighted (IVW) MR analysis and sensitivity tests including MR-Egger and leave-one-out analysis.

Propensity score matching showed that WC was significantly higher in the CAD group compared to controls (p < 0.001). MR analysis confirmed a causal relationship between increased WC and CAD risk, with an estimated causal effect size of 0.02884 (95% CI: 0.016, 0.041; p = 0.00000883). Sensitivity analyses validated the robustness of these findings.

Our results provide strong genetic and observational evidence linking increased WC with a higher risk of CAD. These findings highlight the need for targeted interventions to reduce central obesity and prevent CAD, especially in populations prone to metabolic disorders.

## Linked entities

- **Diseases:** coronary artery disease (MONDO:0005010), diabetes (MONDO:0005015)

## Full-text entities

- **Genes:** LEP (leptin) [NCBI Gene 3952] {aka LEPD, OB, OBS}, MC4R (melanocortin 4 receptor) [NCBI Gene 4160] {aka BMIQ20}, FTO (FTO alpha-ketoglutarate dependent dioxygenase) [NCBI Gene 79068] {aka ALKBH9, BMIQ14, GDFD, IFEX9}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, ADIPOQ (adiponectin, C1Q and collagen domain containing) [NCBI Gene 9370] {aka ACDC, ACRP30, ADIPQTL1, ADPN, APM-1, APM1}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, TMEM18 (transmembrane protein 18) [NCBI Gene 129787] {aka lncND}
- **Diseases:** Central obesity (MESH:D056128), atherosclerotic plaques (MESH:D058226), systemic (MESH:D015619), CAD (MESH:D003324), adiposity (MESH:D018205), Insulin resistance (MESH:D007333), CVD (MESH:D002318), atherogenic (MESH:D050197), hypertension (MESH:D006973), Metabolic dysfunction (MESH:D008659), Obesity (MESH:D009765), waist circumference (MESH:D064250), endothelial dysfunction (MESH:D014652), diabetes (MESH:D003920), Coronary Heart Disease (MESH:D003327), Atherogenic dyslipidemia (MESH:D050171), hyperlipidemia (MESH:D006949), metabolic syndrome (MESH:D024821), inflammation (MESH:D007249)
- **Chemicals:** lipid (MESH:D008055), dense low-density lipoprotein (-), cholesterol (MESH:D002784), triglycerides (MESH:D014280)
- **Mutations:** rs1121980

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12947819/full.md

## References

45 references — full list in the complete paper: https://tomesphere.com/paper/PMC12947819/full.md

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Source: https://tomesphere.com/paper/PMC12947819