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首页> 外文期刊>Iranian journal of public health. >Gene-Gene Interactions among Pparα/δ/γ Polymorphisms for Apolipoprotein (Apo) A-I/Apob Ratio in Chinese Han Population
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Gene-Gene Interactions among Pparα/δ/γ Polymorphisms for Apolipoprotein (Apo) A-I/Apob Ratio in Chinese Han Population

机译:中国汉族人群载脂蛋白(Apo)A-I / Apob比值的Pparα/δ/γ多态性之间的基因-基因相互作用

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BackgroundThe peroxisome proliferator-activated receptors (PPARs) -α, -δ/β and -γ are the ligand-activated transcription factors involved in the regulation of fatty acid and lipoprotein metabolism, energy balance, cell proliferation and differentiation and atherosclerosis, etc. We investigated the associations of 10 single-nucleotide polymorphisms (SNPs) in PPARs with apolipoprotein (apo) A-I/apoB ratio in Chinese Han population.MethodsOverall, 630 subjects (212 males, 418 females) were randomly selected from the Prevention of Metabolic Syndrome and Multiple Metabolic Disorders in Jiangsu Province of China Study Cohort. Population analyzed was as the general population which involved healthy people and individuals with disorders of apoA-I or apoB. 10 SNPs (rs1800206, rs135539, rs4253778, rs2016520, rs9794, rs10865710, rs1805192, rs709158, rs3856806 and rs4684847) were genotyped. Mean difference (Difference) and 95% confident interval (95%CI) were calculated.ResultsAfter covariates adjustment, rs1800206-V allele (LV+VV) and rs3856806-T allele (CT+TT) were significantly associated with a decreased apoA-I/apoB ratio than those wild type carriers, Difference (95%CI) were -1.29 (-1.96—0.62) and -0.8 (-1.42~-0.17), respectively. Rs4253778-C allele was significantly associated with an increased apoA-I/apoB ratio compared to the wild type carriers (GG), Difference (95%CI) was 0.76 (0.04—1.48). Generalized multifactor dimensionality reduction analysis showed that three-to-eight-locus models were significant with apoA-I/apoB ratio (P<0.05). We chose the seven-locus model (P=0.0010) as the best GMDR model (cross-validation consistency was 7/10 and testing accuracy was 62.97%).ConclusionOur data provided the evidence that PPARs polymorphisms might be involved in regulation of apoA-I/apoB ratio in independently and/or in an interactive manner.
机译:背景过氧化物酶体增殖物激活受体(PPAR)-α,-δ/β和-γ是配体激活的转录因子,参与脂肪酸和脂蛋白代谢,能量平衡,细胞增殖和分化以及动脉粥样硬化的调节。方法:调查中国汉族人群中PPARs的10个单核苷酸多态性(SNPs)与载脂蛋白(apo)AI / apoB比的相关性。中国江苏省代谢异常研究队列。分析的人群是包括健康人和患有apoA-I或apoB疾病的个体的总人群。对10个SNP(rs1800206,rs135539,rs4253778,rs2016520,rs9794,rs10865710,rs1805192,rs709158,rs3856806和rs4684847)进行基因分型。结果计算协变量调整后,rs1800206-V等位基因(LV + VV)和rs3856806-T等位基因(CT + TT)与apoA-I降低显着相关,结果显示出均差(差异)和95%置信区间(95%CI)。 / apoB比值比野生型携带者差(95%CI)分别为-1.29(-1.96-0.62)和-0.8(-1.42〜-0.17)。与野生型携带者(GG)相比,Rs4253778-C等位基因与apoA-I / apoB比的增加显着相关,差异(95%CI)为0.76(0.04-1.48)。广义多因素降维分析表明,三到八位基因组模型具有显着的apoA-I / apoB比值(P <0.05)。我们选择七基因座模型(P = 0.0010)作为最佳GMDR模型(交叉验证一致性为7/10,测试准确性为62.97%)。结论我们的数据提供了PPARs多态性可能参与apoA-调控的证据。 I / apoB比率独立和/或以交互方式。

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