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首页> 外文期刊>Cardiovascular Diabetology >Interaction between Calpain 5, Peroxisome proliferator-activated receptor-gamma and Peroxisome proliferator-activated receptor-delta genes: a polygenic approach to obesity
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Interaction between Calpain 5, Peroxisome proliferator-activated receptor-gamma and Peroxisome proliferator-activated receptor-delta genes: a polygenic approach to obesity

机译:Calpain 5,过氧化物酶体增殖物激活的受体-γ和过氧化物酶体增殖物激活的受体-δ基因之间的相互作用:肥胖的一种多基因方法。

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Context Obesity is a multifactorial disorder, that is, a disease determined by the combined effect of genes and environment. In this context, polygenic approaches are needed. Objective To investigate the possibility of the existence of a crosstalk between the CALPAIN 10 homologue CALPAIN 5 and nuclear receptors of the peroxisome proliferator-activated receptors family. Design Cross-sectional, genetic association study and gene-gene interaction analysis. Subjects The study sample comprise 1953 individuals, 725 obese (defined as body mass index ≥ 30) and 1228 non obese subjects. Results In the monogenic analysis, only the peroxisome proliferator-activated receptor delta (PPARD) gene was associated with obesity (OR = 1.43 [1.04–1.97], p = 0.027). In addition, we have found a significant interaction between CAPN5 and PPARD genes (p = 0.038) that reduces the risk for obesity in a 55%. Conclusion Our results suggest that CAPN5 and PPARD gene products may also interact in vivo.
机译:肥胖是一种多因素疾病,即由基因和环境共同作用决定的疾病。在这种情况下,需要多基因方法。目的探讨CALPAIN 10同源CALPAIN 5与过氧化物酶体增殖物激活受体家族的核受体之间存在串扰的可能性。设计横断面,遗传关联研究和基因-基因相互作用分析。受试者该研究样本包括1953名个体,725名肥胖(定义为体重指数≥30)和1228名非肥胖受试者。结果在单基因分析中,只有过氧化物酶体增殖物激活的受体δ(PPARD)基因与肥胖相关(OR = 1.43 [1.04–1.97],p = 0.027)。此外,我们发现CAPN5和PPARD基因之间存在显着的相互作用(p = 0.038),可将肥胖风险降低55%。结论我们的结果表明,CAPN5和PPARD基因产物也可能在体内相互作用。

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