Suppr超能文献

对巴西一个由顶级运动员组成的大型队列中与运动相关的多态性进行分析。

Analysis of sports-relevant polymorphisms in a large Brazilian cohort of top-level athletes.

作者信息

Guilherme João Paulo Limongi França, Bertuzzi Rômulo, Lima-Silva Adriano Eduardo, Pereira Alexandre da Costa, Lancha Junior Antonio Herbert

机构信息

Laboratory of Applied Nutrition and Metabolism, School of Physical Education and Sport, University of Sao Paulo, Sao Paulo, SP, Brazil.

Endurance Performance Research Group, School of Physical Education and Sport, University of São Paulo, São Paulo, SP, Brazil.

出版信息

Ann Hum Genet. 2018 Sep;82(5):254-264. doi: 10.1111/ahg.12248. Epub 2018 Mar 30.

Abstract

In recent years, there have been an increasing number of genetic variants associated with athletic phenotypes. Here, we selected a set of sports-relevant polymorphisms that have been previously suggested as genetic markers for human physical performance, and we examined their association with athletic status in a large cohort of Brazilians. We evaluated a sample of 1,622 individuals, in which 966 were nonathletes, and 656 were athletes: 328 endurance athletes and 328 power athletes. Only the AGT M268T minor allele was nominally associated with the endurance status. Conversely, we found that seven polymorphisms are more frequent in power athletes (MCT1 D490E, AGT M268T, PPARG P12A, PGC1A G482S, VEGFR2 Q472H, NOS3 C/T, and ACTN3 R577X). For all of these polymorphisms, power athletes were more likely than nonathletes or endurance athletes to carry the major allele or the homozygous genotype for the major allele. In particular, MCT1 D490E, AGT M268T, NOS3 C/T, and ACTN3 R577X showed stronger associations. Our findings support a role for these variants in the achievement of power athletic status in Brazilians: MCT1 D490E (T allele), AGT M268T (G allele), PPARG (C allele), PGC1A G482S (C allele), VEGFR2 Q472H (T allele), NOS3 C/T (T allele), and ACTN3 R577X (R allele).

摘要

近年来,与运动表型相关的基因变异数量不断增加。在此,我们选取了一组先前被认为是人类体能遗传标记的与运动相关的多态性位点,并在一大群巴西人中研究了它们与运动状态的关联。我们评估了1622名个体的样本,其中966名是非运动员,656名是运动员:328名耐力运动员和328名力量型运动员。只有AGT M268T次要等位基因名义上与耐力状态相关。相反,我们发现七个多态性位点在力量型运动员中更为常见(MCT1 D490E、AGT M268T、PPARG P12A、PGC1A G482S、VEGFR2 Q472H、NOS3 C/T和ACTN3 R577X)。对于所有这些多态性位点,力量型运动员比非运动员或耐力运动员更有可能携带主要等位基因或主要等位基因的纯合基因型。特别是,MCT1 D490E、AGT M268T、NOS3 C/T和ACTN3 R577X显示出更强的关联性。我们的研究结果支持这些变异在巴西人获得力量型运动状态中发挥的作用:MCT1 D490E(T等位基因)、AGT M268T(G等位基因)、PPARG(C等位基因)、PGC1A G482S(C等位基因)、VEGFR2 Q472H(T等位基因)、NOS3 C/T(T等位基因)和ACTN3 R577X(R等位基因)。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验