Evidence map›Paper›PMID 38987727›Full record

ArticleBMC endocrine disorders2024

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.

Guillermo Celestino Cardoso-Saldaña, Neftali Eduardo Antonio-Villa, María Del Rocío Martínez-Alvarado, María Del Carmen González-Salazar, Rosalinda Posadas-Sánchez

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Article in BMC endocrine disorders, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Guillermo Celestino Cardoso-SaldañaDepartment of Endocrinology, National Institute of Cardiology Ignacio Chávez, Juan Badiano No. 1, Col Sección XVI, CP 14080, Tlalpan, México City, Mexico. gccardosos@yahoo.com.
Neftali Eduardo Antonio-VillaDepartment of Endocrinology, National Institute of Cardiology Ignacio Chávez, Juan Badiano No. 1, Col Sección XVI, CP 14080, Tlalpan, México City, Mexico.
María Del Rocío Martínez-AlvaradoDepartment of Endocrinology, National Institute of Cardiology Ignacio Chávez, Juan Badiano No. 1, Col Sección XVI, CP 14080, Tlalpan, México City, Mexico.
María Del Carmen González-SalazarDepartment of Endocrinology, National Institute of Cardiology Ignacio Chávez, Juan Badiano No. 1, Col Sección XVI, CP 14080, Tlalpan, México City, Mexico.
Rosalinda Posadas-SánchezDepartment of Endocrinology, National Institute of Cardiology Ignacio Chávez, Juan Badiano No. 1, Col Sección XVI, CP 14080, Tlalpan, México City, Mexico.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe 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.

methodsIn 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.

resultsBody 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 < 0.001). This association was independent of classical coronary risk factors, visceral and pericardial fat measurements.

conclusionThe HDL-C/ApoA-I index is inversely associated with an adverse cardiometabolic profile and CAC score, making it a potentially useful and practical biomarker of coronary atherosclerosis. Overall, these findings suggest that the HDL-C/ApoA-I index could be useful for evaluating the probability of having higher cardiometabolic risk factors and subclinical atherosclerosis in adults without CAD.

Indexed as

Apolipoprotein A-ICardiometabolic Risk FactorsCholesterol, HDLCoronary Artery DiseaseAdultAgedAtherosclerosisBiomarkersCoronary VesselsCross-Sectional StudiesFemaleHumansMaleMetabolic SyndromeMiddle AgedRisk FactorsAPOA1 protein, humanApolipoprotein A-IBiomarkersCholesterol, HDLCoronary artery calcium scoreHDL-C/Apo-AI indexHeart disease biomarker

Identifiers

PMID38987727
PMCPMC11238479

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.