Department of Family Medicine, CHA Bundang Medical Center, CHA University, Seongnam-si 13496, Korea.
Department of Family Medicine, Wonju Severance Christian Hospital, Yonsei University Wonju College of Medicine, Wonju-si 26426, Korea.
Int J Mol Sci. 2022 Oct 6;23(19):11889. doi: 10.3390/ijms231911889.
Although many genome-wide association studies (GWASs) have evaluated the association with metabolic disorders, the current study is the first attempt to analyze the genetic risk factors for various metabolic disorders according to sex and age groups of the life course in Korean adults. A total population of 50,808 people were included in this GWAS. The genetic traits for eight metabolic phenotypes were investigated in peri-, and postmenopausal women compared to a younger group or men of corresponding age groups. The metabolic phenotypes include general obesity, abdominal obesity, hypertension, type 2 diabetes, hypercholesterolemia, hypertriglyceridemia, hypo-high-density lipoprotein cholesterolemia, and metabolic syndrome. In the total participants, GWAS results for eight metabolic phenotypes found 101 significant loci. Of these, 15 loci were the first reported to be associated with the risk of metabolic disorder. Interestingly, some of the significant loci presented the association with the various phenotypes, which presented when there was a correlation between phenotypes. In addition, we analyzed divided by gender and age (young adult, peri-menopausal group, older adult), and specifically identified specific loci in peri-menopausal women. Meanwhile, several genetic factors associated with metabolic disorders were newly reported in our study. In particular, several genes were significantly associated with one of the metabolic phenotypes in only a single specific group. These findings suggest that menopausal transition rather than aging itself potentiates the influence of genetic risks on metabolic disorders. In addition, some genetic loci with low frequencies may play a role in the metabolic disturbances in a specific sex and age group. The genetic traits derived from our study may contribute to understanding the genetic risk factors for metabolic disorders in the Korean population.
尽管许多全基因组关联研究(GWAS)已经评估了代谢紊乱与遗传的相关性,但本研究首次尝试根据韩国成年人生命历程的性别和年龄组分析各种代谢紊乱的遗传风险因素。本 GWAS 共纳入了 50808 人。与年轻组或相应年龄组的男性相比,研究人员比较了绝经前和绝经后女性的 8 种代谢表型的遗传特征。代谢表型包括一般肥胖、腹部肥胖、高血压、2 型糖尿病、高胆固醇血症、高三酰甘油血症、低高密度脂蛋白胆固醇血症和代谢综合征。在所有参与者中,针对 8 种代谢表型的 GWAS 结果发现了 101 个显著位点。其中,有 15 个位点是首次报道与代谢紊乱风险相关的。有趣的是,一些显著位点与各种表型存在关联,而这些表型之间存在相关性。此外,我们还按性别和年龄(年轻成年人、绝经前组、老年人)进行了分析,并特别确定了绝经前女性的特定位点。同时,在我们的研究中,有几个与代谢紊乱相关的遗传因素是新报道的。特别是,几个基因仅与一个特定表型存在显著关联。这些发现表明,绝经过渡而不是衰老本身增强了遗传风险对代谢紊乱的影响。此外,一些低频遗传位点可能在特定性别和年龄组的代谢紊乱中发挥作用。本研究得出的遗传特征可能有助于了解韩国人群代谢紊乱的遗传风险因素。