Institute of Bioinformatics, University of Georgia, Athens, Georgia, United States of America.
Department of Epidemiology, Tulane University School of Public Health and Tropical Medicine, New Orleans, Louisiana, United States of America.
PLoS Genet. 2021 Mar 24;17(3):e1009431. doi: 10.1371/journal.pgen.1009431. eCollection 2021 Mar.
Fish oil supplementation is widely used for reducing serum triglycerides (TAGs) but has mixed effects on other circulating cardiovascular biomarkers. Many genetic polymorphisms have been associated with blood lipids, including high- and low-density-lipoprotein cholesterol (HDL-C, LDL-C), total cholesterol, and TAGs. Here, the gene-diet interaction effects of fish oil supplementation on these lipids were analyzed in a discovery cohort of up to 73,962 UK Biobank participants, using a 1-degree-of-freedom (1df) test for interaction effects and a 2-degrees-of-freedom (2df) test to jointly analyze interaction and main effects. Associations with P < 1×10-6 in either test (26,157; 18,300 unique variants) were advanced to replication in up to 7,284 participants from the Atherosclerosis Risk in Communities (ARIC) Study. Replicated associations reaching 1df P < 0.05 (2,175; 1,763 unique variants) were used in meta-analyses. We found 13 replicated and 159 non-replicated (UK Biobank only) loci with significant 2df joint tests that were predominantly driven by main effects and have been previously reported. Four novel interaction loci were identified with 1df P < 5×10-8 in meta-analysis. The lead variant in the GJB6-GJB2-GJA3 gene cluster, rs112803755 (A>G; minor allele frequency = 0.041), shows exclusively interaction effects. The minor allele is significantly associated with decreased TAGs in individuals with fish oil supplementation, but with increased TAGs in those without supplementation. This locus is significantly associated with higher GJB2 expression of connexin 26 in adipose tissue; connexin activity is known to change upon exposure to omega-3 fatty acids. Significant interaction effects were also found in three other loci in the genes SLC12A3 (HDL-C), ABCA6 (LDL-C), and MLXIPL (LDL-C), but highly significant main effects are also present. Our study identifies novel gene-diet interaction effects for four genetic loci, whose effects on blood lipids are modified by fish oil supplementation. These findings highlight the need and possibility for personalized nutrition.
鱼油补充剂被广泛用于降低血清甘油三酯(TAGs),但对其他循环心血管生物标志物的影响不一。许多基因多态性与血脂有关,包括高密度脂蛋白胆固醇(HDL-C)、低密度脂蛋白胆固醇(LDL-C)、总胆固醇和 TAGs。在这里,使用 1 度自由度(1df)交互作用检验和 2 度自由度(2df)检验来共同分析交互作用和主要效应,在多达 73962 名英国生物库参与者的发现队列中分析了鱼油补充剂对这些脂质的基因-饮食相互作用效应。在这两种检验中,关联 P 值小于 1×10-6(26157 个;18300 个独特变体)被推进到动脉粥样硬化风险社区(ARIC)研究中的 7284 名参与者中进行复制。达到 1df P < 0.05(2175 个;1763 个独特变体)的重复关联用于荟萃分析。我们发现了 13 个重复和 159 个非重复(仅英国生物库)与 2df 联合检验显著相关的基因座,这些基因座主要由主要效应驱动,并且之前已有报道。在荟萃分析中,我们鉴定了 4 个具有 1df P < 5×10-8 的新的交互作用基因座。GJB6-GJB2-GJA3 基因簇中的主要变异 rs112803755(A>G;次要等位基因频率=0.041),仅表现出交互作用。在补充鱼油的个体中,该等位基因与 TAGs 的降低显著相关,但在未补充鱼油的个体中与 TAGs 的增加显著相关。该基因座与脂肪组织中连接蛋白 26 的 GJB2 表达显著相关;已知连接蛋白活性在暴露于 ω-3 脂肪酸时会发生变化。在 SLC12A3(HDL-C)、ABCA6(LDL-C)和 MLXIPL(LDL-C)基因中的其他三个基因座也发现了显著的交互作用效应,但也存在高度显著的主要效应。我们的研究确定了四个遗传基因座的新型基因-饮食相互作用效应,其对血脂的影响受鱼油补充的调节。这些发现突出了个性化营养的必要性和可能性。