4.5 Article

Causal effects of plasma lipids on the risk of atrial fibrillation: A multivariable mendelian randomization study

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ELSEVIER SCI LTD
DOI: 10.1016/j.numecd.2021.02.011

关键词

Plasma lipids; Atrial fibrillation; Causal effect; Mendelian randomization

资金

  1. Science and Technology Project for Youth Talent of Changzhou Health Commission [QN201801]
  2. Young Talent Development Plan of Changzhou Health Commission [CZQM2020051]
  3. Science and Technology Support Project of Bureau of Science and Technology of Changzhou [CE20195044]
  4. Changzhou Key Research and Development Program of Applied Basic Research [CJ20209026]
  5. National Natural Science Foundation of China [81900295]
  6. Natural Science Foundation of Jiangsu Province of China [BK20191071]

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The study provides strong evidence that high Lp(a) increases the risk of AF. No other lipid components were causally associated with AF, CES, or HF, except for a marginal association between triglycerides and HF.
Background and aims: Observational studies have suggested that plasma lipids contribute substantially to cardiovascular disease, but cholesterol paradox in atrial fibrillation (AF) remains. We sought to investigate the causal effects of lipid profiles on the risk of AF. Methods and results: Two-sample Mendelian randomization (MR) framework was implemented to examine the causality of association. Summary estimations of genetic variants associated with low density lipoprotein (LDL)-cholesterol, high density lipoprotein (HDL)-cholesterol, total cholesterol, triglycerides, lipoprotein-a [Lp(a)], apolipoprotein A1 (ApoA 1), and apolipoprotein B (ApoB) were 81, 99, 96, 61, 30, 10, and 23 single nucleotide polymorphisms, respectively. Genetic association with AF were retrieved from a genome-wide association study that included 1,030,836 individuals. The complications for AF were predefined as cardioembolic stroke (CES) and heart failure (HF). In the multivariable MR, the odds ratios for AF per standard deviation (SD) increase were 1.030 (95% confidence interval (CI) 0.979-1. 083; P = 0.257) for LDLcholesterol, 0.986 (95% CI 0.931-1.044; P = 0.622) for HDL-cholesterol, 0.965 (95% CI 0.896-1.041; P = 0.359) for triglycerides, 1.001 (95% CI 1.000-1.003 ; P = 0.023) for Lp(a), 1.017 (95% CI 0.966-1.070; P = 0.518) for ApoA1, and 1.002 (95% CI 0.963-1.043; P = 0.923) for ApoB. There was no evidence that other lipid components were causally associated with AF, CES, or HF, other than for a marginal association between triglycerides and HF. Conclusions: This MR study provides robust evidence that high Lp(a) increases the risk of AF, suggesting that interventions targeting Lp(a) may contribute to the primary prevention of AF. (c) 2021 The Italian Diabetes Society, the Italian Society for the Study of Atherosclerosis, the Italian Society of Human Nutrition and the Department of Clinical Medicine and Surgery, Federico II University. Published by Elsevier B.V. All rights reserved.

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