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PPARγ2 C1431T 基因型增加低心肺适能年轻男性代谢综合征风险。

PPARγ2 C1431T genotype increases metabolic syndrome risk in young men with low cardiorespiratory fitness.

机构信息

College of Sport and Health Science, Ritsumeikan University, Shiga, Japan.

出版信息

Physiol Genomics. 2011 Feb 11;43(3):103-9. doi: 10.1152/physiolgenomics.00129.2010. Epub 2010 Dec 14.

Abstract

The peroxisome proliferator-activated receptor gamma 2 (PPARγ2) genotypes are related to obesity and the metabolic syndrome (MetS). A low level of cardiorespiratory fitness is also a strong determining factor in the development of MetS. This cross-sectional study was performed to investigate the influence of the interaction between the PPARγ2 genotype and cardiorespiratory fitness on the risk of MetS. Healthy Japanese men (n = 211) and women (n = 505) participated in this study. All subjects were divided into 8 groups according to sex, fitness level (high and low fitness groups), and age (younger, age < 40 yr; middle-aged/older, age ≥ 40 yr). The PPARγ2 genotypes (Pro12Ala and C1431T) were analyzed by real-time PCR with Taq-Man probes. Two-way ANCOVA with adjustment for age as a covariate indicated that fitness and the CC genotype of C1431T in the PPARγ2 gene interacted to produce a significant effect on MetS risk in younger men and that the risk of MetS in the CC genotype group with low cardiorespiratory fitness was significantly higher than that in the corresponding CT+TT genotypes or in the high fitness groups. There was no significant interaction between fitness and genotype in determining MetS risk in middle-aged/older men or in women in any group. With regard to the Pro12Ala genotype of the PPARγ2 gene, there were no significant differences in fitness or genotype effects nor were there any interactions between measurement variables. We concluded that the CC genotype of C1431T in the PPARγ2 gene together with low cardiorespiratory fitness may increase the risk of MetS in younger men (age < 40 yr), even with adjustment for age.

摘要

过氧化物酶体增殖物激活受体γ 2(PPARγ2)基因型与肥胖和代谢综合征(MetS)有关。心肺功能适应性低也是 MetS 发展的一个重要决定因素。本横断面研究旨在探讨 PPARγ2 基因型与心肺功能适应性之间的相互作用对 MetS 风险的影响。健康的日本男性(n = 211)和女性(n = 505)参加了这项研究。所有受试者均根据性别、身体适应水平(高和低适应组)和年龄(年轻,年龄<40 岁;中年/老年,年龄≥40 岁)分为 8 组。通过实时 PCR 用 Taq-Man 探针分析 PPARγ2 基因型(Pro12Ala 和 C1431T)。协方差分析(ANCOVA)表明,适应性和 PPARγ2 基因中的 C1431T CC 基因型之间存在相互作用,对年轻男性的 MetS 风险产生显著影响,且低心肺功能适应性的 CC 基因型组发生 MetS 的风险明显高于相应的 CT+TT 基因型或高适应组。在中年/老年男性或任何组别的女性中,适应性和基因型在确定 MetS 风险方面没有显著的相互作用。关于 PPARγ2 基因的 Pro12Ala 基因型,适应性或基因型效应均无显著差异,也不存在测量变量之间的相互作用。我们得出结论,PPARγ2 基因的 C1431T CC 基因型加上低心肺功能适应性可能会增加年轻男性(年龄<40 岁)的 MetS 风险,即使调整了年龄因素。

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