Key result
Visceral adipose tissue showed a positive association with left ventricular global longitudinal strain (β = 0.482) and mediated 60.9% of the total effect between insulin resistance and LV-GLS.
Why the study?
The relationship between visceral adipose tissue, cardiac dysfunction, and the mediation capacity of visceral adipose tissue related to insulin resistance has not been fully characterized.
Cross-Sectional (n=195)
Yes
Effect estimate: β = 0.482 (95% CI 0.060-0.904)
p-value: p=0.039
Visceral adiposity is independently associated with subclinical left ventricular dysfunction (impaired LV-GLS) and strongly mediates the relationship between insulin resistance and myocardial dysfunction in patients with type 2 diabetes.
BACKGROUND: Adipose tissue distribution plays a crucial role in the development of cardiovascular complications. In particular, visceral adipose tissue (VAT) has been linked to insulin resistance (IR) and cardiovascular disease (CVD). However, the relationship between VAT, cardiac dysfunction and the meditation capacity of VAT related to IR has not been fully characterized. METHODS: This cross-sectional study included adults living with type 2 diabetes (T2D). VAT was measured using electrical bioimpedance and also estimated with the Metabolic Score for Visceral Fat (METS-VF). LV function was assessed using left ventricular global longitudinal strain (LV-GLS) by speckle tracking echocardiography analysis. Spearman correlation coefficients, adjusted linear regression models guided by direct acyclic diagrams and causal mediation analysis were performed. RESULTS: Among 195 adults living with T2D (median age: 57, IQR: 49-64, women: 63%), VAT showed a positive association with LV-GLS (β = 0.482, 95% CI: 0.060-0.904, p = 0.039) after adjusting for relevant confounders. The effect was strongly replicated using METS-VF as a surrogate for VAT. The mediation analysis revealed that VAT accounted for 60.9% (95% CI: 15.82-171) of the total effect between IR and LV-GLS. CONCLUSION: This study demonstrated a positive association between VAT and LV-GLS. This relationship was consistently observed using the clinical surrogate METS-VF. Visceral adiposity was identified as a strong mediator in the relationship between IR and LV-GLS, underscoring its role in the pathophysiology of cardiovascular disease in patients with T2D.
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Martinez‐Dominguez et al. (2025) conducted a cross-sectional in Type 2 diabetes (n=195). Visceral adipose tissue (VAT) vs. Lower visceral adipose tissue was evaluated on Left ventricular global longitudinal strain (LV-GLS) (β = 0.482, 95% CI 0.060-0.904, p=0.039). Visceral adipose tissue showed a positive association with left ventricular global longitudinal strain (β = 0.482) and mediated 60.9% of the total effect between insulin resistance and LV-GLS.
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