线粒体GWA分析在几种复杂疾病中使用KORA人群

A. Flaquer, K. Ladwig, M. Waldenberger, H. Grallert, C. Meisinger, T. Meitinger, A. Peters, K. Strauch
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引用次数: 0

摘要

目的:我们的主要目标是鉴定人类复杂疾病的线粒体易感基因。方法:使用不同的基因分型平台和新一代测序,我们对具有几种表型(BMI、胆固醇、创伤后应激障碍、甲状腺疾病、抑郁症等)以及生活方式(吸烟、饮酒和体育活动)的KORA人群(3,080人)进行了mtGWA分析。结果:我们报告了与创伤后应激障碍和代谢综合征相关的几个线粒体遗传变异。BMI、HDL胆固醇和TG水平也与线粒体变异相关,表明这些变异的异质性可能影响HDL胆固醇和TG水平的平衡。我们还观察到,不运动、酗酒和吸烟可能会增加线粒体遗传变异的异质性水平。结论:由于mtDNA异质性的波动可能意味着细胞活性的改变,我们的研究结果强调了mtDNA作为衰老相关疾病和代谢综合征的生物标志物的重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mitochondrial GWA analysis in several complex diseases using the KORA population
Objectives: Our main goal is to identify mitochondrial susceptibility genes for human complex diseases. Methodology: Using different genotyping platforms and New Generation Sequencing we performed mtGWA analysis in the KORA population (3,080 individuals) with several phenotypes (BMI, cholesterol, post-traumatic stress disorder, thyroid diseases, depression, among others) as well as with life styles (smoking cigarettes, alcohol consumption, and physical activity). Results: we report several mitochondrial genetic variants associated with post-traumatic stress disorders and metabolic syndrome. BMI, HDL cholesterol and TG levels were also associated to mitochondrial variants, indicating that the presence of heteroplasmy in these variants may influence the balance of HDL cholesterol and TG levels. We also observed that no physical activity, alcohol abuse, and smoke cigarettes may increase the heteroplasmy levels of mitochondrial genetic variants. Conclusions: As fluctuations in mtDNA heteroplasmy may signify alterations in cellular activity, our findings highlight the important role of the mtDNA as a biomarker for aging-related diseases and metabolic syndromes.
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