脂质组和全基因组研究了解循环脂质的性别差异

R. Tabassum, S. Ruotsalainen, L. Ottensmann, M. Gerl, C. Klose, T. Tukiainen, M. Pirinen, K. Simons, E. Widén, S. Ripatti
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引用次数: 9

摘要

尽管动脉粥样硬化性心血管疾病(ASCVD)的风险在男性和女性之间存在明显的差异,但在ASCVD的病理生理中,风险因素的性别差异和性别特异性机制仍然知之甚少。脂质代谢在ASCVD的发展中起核心作用。了解脂质及其遗传决定因素的性别差异可以为ASCVD的性别差异提供机制见解,并有助于精确的风险评估。因此,我们检查了来自7266名参与者的179种脂质血浆水平的性别差异,并进行了性别分层全基因组关联研究(GWAS),以评估遗传因素在性别差异中的作用。我们使用来自2,045名参与者的独立数据寻求复制。141种脂质在性别上存在显著差异(P<7.0 × 10-4)。有趣的是,121种脂质表现出显著的年龄-性别相互作用,39种脂质表现出相反的年龄相关变化。总体而言,45-50岁男性的胆固醇酯、神经酰胺、溶血磷脂和甘油脂含量高于同龄女性,但性别差异随着年龄的增长而缩小或逆转。在性别分层的GWAS中,我们没有观察到遗传效应的任何主要差异,这表明常见的遗传变异在脂质组的性别差异中没有主要作用。总之,我们的研究提供了循环脂质的性别差异的综合观点,指出了脂质代谢的潜在性别差异,并强调了针对性别和年龄的预防策略的必要性。
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Lipidome‐ and Genome‐Wide Study to Understand Sex Differences in Circulatory Lipids
Despite well-recognized difference in the atherosclerotic cardiovascular disease (ASCVD) risk between men and women, sex differences in risk factors and sex specific mechanisms in the pathophysiology of ASCVD remain poorly understood. Lipid metabolism plays a central role in the development of ASCVD. Understanding sex differences in lipids and their genetic determinants could provide mechanistic insights into sex differences in ASCVD and aid in precise risk assessment. Thus, we examined sex differences in plasma levels of 179 lipid species from 7,266 participants and performed sex-stratified genome-wide association studies (GWAS) to evaluate contribution of genetic factors in sex differences. We sought for replication using independent data from 2,045 participants. Significant sex differences in levels of 141 lipid species were observed (P<7.0x10-4). Interestingly, 121 lipid species showed significant age-sex interactions with opposite age-related changes in 39 lipid species. In general, most of the cholesteryl esters, ceramides, lysophospholipids and glycerides were higher in 45-50-year-old men compared with women of same age, but the sex-differences narrowed down or reversed with age. We did not observe any major differences in genetic effect in the sex stratified GWAS which suggests that common genetic variants do not have a major role in sex differences in lipidome. In conclusion, our study provides a comprehensive view of sex differences in circulatory lipids pointing to potential sex differences in lipid metabolism, and highlights need for sex- and age-specific prevention strategies.
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