Department of Preventive Medicine, Faculty of Medicine, Saga University, Saga, Japan.
Division of Biomedical Information Analysis, Iwate Tohoku Medical Megabank Organization, Disaster Reconstruction Center, Iwate Medical University, Iwate, Japan.
J Lipid Res. 2020 Jan;61(1):86-94. doi: 10.1194/jlr.P091546. Epub 2019 Nov 6.
Few studies have investigated the interactions between HDL-C-related SNPs identified by genome-wide association (GWA) study and physical activity (PA) on HDL-C. First, we conducted a sex-stratified GWA study in a discovery sample (2,231 men and 2,431 women) and replication sample (2,599 men and 3,109 women) to identify SNPs influencing log-transformed HDL-C in Japanese participants in the baseline survey of the Japan Multi-Institutional Collaborative Cohort Study. We also replicated previously reported HDL-C-related SNPs in a combined (discovery plus replication) sample (4,830 men and 5,540 women). We then analyzed the interactions of the HDL-C-related SNPs with PA on HDL-C. The sex-stratified GWA analyses identified 11 and 10 HDL-C-related SNPs in men and women as targets for an interaction analysis. Among these, only one interaction of ABCA1 rs1883025 with PA was statistically significant in men, after Bonferroni correction [-interaction = 0.001 (α = 0.05/21 = 0.002)]. The per-major-allele (C allele) increase in log-transformed HDL-C was lost in men with low PA (β = 0.008) compared with those with medium (β = 0.032) or high PA (β = 0.034). These findings suggest that the benefit of carrying a C allele of ABCA1 rs1883025 on enhancing HDL-C may be attenuated in inactive men.
很少有研究调查全基因组关联(GWA)研究确定的高密度脂蛋白胆固醇(HDL-C)相关单核苷酸多态性(SNP)与体力活动(PA)之间的相互作用。首先,我们在发现样本(2231 名男性和 2431 名女性)和复制样本(2599 名男性和 3109 名女性)中进行了性别分层 GWA 研究,以鉴定影响日本多机构合作队列研究基线调查中日本参与者 log 转化的 HDL-C 的 SNP。我们还在合并(发现加复制)样本(4830 名男性和 5540 名女性)中复制了先前报道的与 HDL-C 相关的 SNP。然后,我们分析了 HDL-C 相关 SNP 与 PA 对 HDL-C 的相互作用。性别分层 GWA 分析确定了 11 个和 10 个男性和女性的 HDL-C 相关 SNP 作为相互作用分析的目标。在这些 SNP 中,只有 ABCA1 rs1883025 与 PA 的相互作用在男性中具有统计学意义,经过 Bonferroni 校正后[相互作用=0.001(α=0.05/21=0.002)]。与中(β=0.032)或高(β=0.034)PA 相比,低 PA 男性(β=0.008)的 log 转化 HDL-C 主要等位基因(C 等位基因)增加量丢失。这些发现表明,在不活跃的男性中,携带 ABCA1 rs1883025 的 C 等位基因对增强 HDL-C 的益处可能会减弱。