Key result
Higher central adiposity is linked to an ~84% narrower genetic risk gap in AIP.
Why the study?
Composite lipid-glucose indices are often interpreted as uniform metabolic signals regardless of body fat distribution, prompting evaluation of whether their behavior varies with central adiposity and genetic risk.
Cross-Sectional (n=396)
No
Effect estimate: β 0.0449 (95% CI 0.0199-0.0700)
p-value: p=<0.001
Identical composite lipid-glucose index values (AIP, TyG) can represent different metabolic and genetic contexts depending on an individual's central adiposity, highlighting the need to interpret these indices alongside adiposity measures.
Central adiposity may modify AIP and TyG interpretation; leaves open whether wGRS should refine their use in risk assessment.
Introduction Central adiposity is a major determinant of cardiometabolic risk. However, routinely used composite lipid–glucose indices are often interpreted to indicate a uniform metabolic signal across individuals with different body fat distributions. This study examined whether the interpretive behavior of the atherogenic index of plasma (AIP) and the triglyceride–glucose (TyG) index varies with central adiposity and the evaluated three-variant triglyceride-weighted genetic risk score (wGRS) in Mexican adults. Methods A cross-sectional analytical design was applied to data from 396 participants stratified by waist-to-height ratio (WHtR), incorporating correlation structure, an exploratory WHtR × wGRS interaction, and distributional analyses. Results Across WHtR tertiles, AIP was higher in the upper tertiles than in the lowest, with minimal additional separation between the intermediate and highest groups, and TyG showed the same upper-versus-lower tertile pattern. Sex-stratified predictions from the continuous interaction models showed that the absolute difference in AIP between wGRS levels of −1 SD and +1 SD narrowed from 0.91 to 0.15 z-score units in men and from 0.32 to 0.03 in women as WHtR increased from −1 SD to +1 SD. Distributional analyses revealed persistent within-stratum overlap, indicating metabolic heterogeneity despite similar anthropometric classifications. Discussion Identical AIP or TyG values may occur across different adiposity levels and degrees of wGRS-related separation within the evaluated population, supporting interpretation of these indices in relation to central adiposity.
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Hernández‐Guerrero et al. (2026) conducted a cross-sectional in Central adiposity and metabolic risk (n=396). Central adiposity (waist-to-height ratio) and triglyceride-weighted genetic risk score vs. Lower waist-to-height ratio and lower genetic risk score was evaluated on WHtR × wGRS interaction on Atherogenic index of plasma (AIP) (β 0.0449, 95% CI 0.0199-0.0700, p=<0.001).
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