Apolipoprotein A-I concentrations and risk of coronary artery disease: A Mendelian randomization study.

Minna K Karjalainen; Michael V Holmes; Qin Wang; Olga Anufrieva; Mika Kähönen; Terho Lehtimäki; Aki S Havulinna; Kati Kristiansson; Veikko Salomaa; Markus Perola; Jorma S Viikari; Olli T Raitakari; Marjo-Riitta Järvelin; Mika Ala-Korpela; Johannes Kettunen
Abstract
Apolipoprotein A-I (apoA-I) infusions represent a potential novel therapeutic approach for the prevention of coronary artery disease (CAD). Although circulating apoA-I concentrations inversely associate with risk of CAD, the evidence base of this representing a causal relationship is lacking. The aim was to assess the causal role of apoA-I using human genetics.We identified a variant (rs12225230) in APOA1 locus that associated with circulating apoA-I concentrations (p < 5 × 10) in 20,370 Finnish participants, and meta-analyzed our data with a previous GWAS of apoA-I. We obtained genetic estimates of CAD from UK Biobank and CARDIoGRAMplusC4D (totaling 122,733 CAD cases) and conducted a two-sample Mendelian randomization analysis. We compared our genetic findings to observational associations of apoA-I with risk of CAD in 918 incident CAD cases among 11,535 individuals from population-based prospective cohorts.-8ApoA-I was associated with a lower risk of CAD in observational analyses (HR 0.81; 95%CI: 0.75, 0.88; per 1-SD higher apoA-I), with the association showing a dose-response relationship. Rs12225230 associated with apoA-I concentrations (per-C allele beta 0.076 SD; SE: 0.013; p = 1.5 × 10) but not with confounders. In Mendelian randomization analyses, apoA-I was not related to risk of CAD (OR 1.13; 95%CI: 0.98,1.30 per 1-SD higher apoA-I), which was different from the observational association. Similar findings were observed using an independent ABCA1 variant in sensitivity analysis.-9Genetic evidence fails to support a cardioprotective role for apoA-I. This is in line with the cumulative evidence showing that HDL-related phenotypes are unlikely to have a protective role in CAD.
Journal ATHEROSCLEROSIS
ISSN 1879-1484
Published 14 Feb 2020
Volume
Issue
Pages
DOI 10.1016/j.atherosclerosis.2020.02.002
Type Journal Article
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