Key result
Higher Visceral Adiposity Index was associated with an increased risk of cardiac death (HR 3.402; 95% CI 2.123-5.449; P<0.001) and heart failure readmission in patients with MetS and HFrEF.
Why the study?
The association between the visceral adiposity index and poor prognosis in patients with metabolic syndrome and HFrEF remained unclear.
Does higher Visceral Adiposity Index (VAI) predict increased risk of cardiac death and heart failure readmission in patients with metabolic syndrome and HFrEF?
Cohort (n=809)
No
Does higher Visceral Adiposity Index (VAI) predict increased risk of cardiac death and heart failure readmission in patients with metabolic syndrome and HFrEF?
Hazard Ratio: 3.402 (95% CI 2.123–5.449)
p-value: p=< 0.001
Higher Visceral Adiposity Index is an independent predictor of cardiac death and heart failure readmission in patients with HFrEF and metabolic syndrome.
May refine prognosis in MetS-HFrEF; leaves open whether visceral adiposity is modifiable or causal.
BACKGROUND: Visceral Adiposity Index (VAI) is an effective predictor of metabolic syndrome (MetS) and serves as a marker of visceral adiposity. The association between the VAI index and poor prognosis in patients with MetS and Heart failure with reduced ejection fraction (HFrEF) remains unclear. The aim of this study is to evaluate the relationship between VAI and endpoint events in patients with metabolic syndrome and HFrEF. METHODS: This study was a single-center retrospective cohort study. A total of 809 patients with MetS and HFrEF admitted to Hangzhou Hospital of Zhejiang Medical Group from January 2014 to September 2021 were consecutively included. The VAI index was calculated based on anthropometric measurements and laboratory examination results at admission, and patients were grouped according to tertiles of VAI index. All patients were followed for 24 months, and the incidence of cardiac death and readmission for heart failure was recorded. RESULTS: For different clinical endpoint events, there were significant differences in event-free survival between tertiles of VAI index. The risk of cardiac death [hazard ratio (HR):3.402, 95%CI:2.123-5.449, P < 0.001] and heart failure readmission (HR:4.862, 95%CI:3.605-6.557, P < 0.001) increased with the increase of tertile of VAI index. Multivariate COX regression analysis adjusted for other confounding factors showed that VAI was an independent predictor of clinical adverse endpoint events. The predictive value of VAI for cardiac death [Area under curve (AUC):0.649, 95%CI:0.602-0.697, P < 0.001] and heart failure readmission (AUC:0.693, 95%CI:0.656-0.729, P < 0.001) was higher than that of other variables. CONCLUSIONS: In patients with HFrEF at risk for comorbid metabolic diseases, baseline VAI levels on admission were associated with the occurrence of adverse outcomes during follow-up.
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Wu et al. (2025) conducted a cohort in Metabolic syndrome and heart failure with reduced ejection fraction (HFrEF) (n=809). Visceral Adiposity Index (VAI) vs. Lower tertiles of VAI was evaluated on Cardiac death (HR 3.402, 95% CI 2.123-5.449, p=< 0.001). Higher Visceral Adiposity Index was associated with an increased risk of cardiac death (HR 3.402; 95% CI 2.123-5.449; P<0.001) and heart failure readmission in patients with MetS and HFrEF.
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