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Low HDL-C/ApoA-I index is associated with cardiometabolic risk factors and coronary artery calcium: a sub-analysis of the genetics of atherosclerotic disease (GEA) study

Authors :
Guillermo Celestino Cardoso-Saldaña
Neftali Eduardo Antonio-Villa
María del Rocío Martínez-Alvarado
María del Carmen González-Salazar
Rosalinda Posadas-Sánchez
Source :
BMC Endocrine Disorders, Vol 24, Iss 1, Pp 1-10 (2024)
Publication Year :
2024
Publisher :
BMC, 2024.

Abstract

Abstract Background The high-density lipoprotein cholesterol to apolipoprotein A-I index (HDL-C/ApoA-I) may be practical and useful in clinical practice as a marker of atherosclerosis. This study aimed to investigate the association between the HDL-C/ApoA-I index with cardiometabolic risk factors and subclinical atherosclerosis. Methods In this cross-sectional sub-analysis of the GEA study, 1,363 individuals, women (51.3%) and men (48.7%) between 20 and 75 years old, without coronary heart disease or diabetes mellitus were included. We defined an adverse cardiometabolic profile as excess adipose tissue metrics, non-alcoholic liver fat measured by non-contrasted tomography, metabolic syndrome, dyslipidemias, and insulin resistance. The population was stratified by quartiles of the HDL-C/Apo-AI index, and its dose-relationship associations were analysed using Tobit regression, binomial, and multinomial logistic regression analysis. Results Body mass index, visceral and pericardial fat, metabolic syndrome, fatty liver, high blood pressure, and CAC were inversely associated with the HDL-C/ApoA-I index. The CAC > 0 prevalence was higher in quartile 1 (29.2%) than in the last quartile (22%) of HDL-C/ApoA-I index (p = 0.035). The probability of having CAC > 0 was higher when the HDL-C/ApoA-I index was less than 0.28 (p

Details

Language :
English
ISSN :
14726823
Volume :
24
Issue :
1
Database :
Directory of Open Access Journals
Journal :
BMC Endocrine Disorders
Publication Type :
Academic Journal
Accession number :
edsdoj.88c0bf1efd5c47dca49d4647c3a6f6d5
Document Type :
article
Full Text :
https://doi.org/10.1186/s12902-024-01642-0