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首页> 外文期刊>Human Molecular Genetics >Haplotypic analyses of the IGF2-INS-TH gene cluster in relation to cardiovascular risk traits.
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Haplotypic analyses of the IGF2-INS-TH gene cluster in relation to cardiovascular risk traits.

机译:IGF2-INS-TH基因簇与心血管疾病危险性状的单倍型分析。

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The IGF2-INS-TH genomic region has been implicated in various common disorders including the metabolic syndrome, type 2 diabetes and coronary heart disease (CHD). Here we present detailed haplotype analysis of 2743 males 51-62 years old in relation to body weight and composition, blood pressure (BP) and plasma triglycerides (TG). Use of the total data set was complicated by the number of loci typed, missing data, multi-allelic markers and continuous trait phenotypes. Different algorithms and subsets of the data were analysed using the programmes haplotype trend regression, haplo.score, evolutionary-based haplotype analysis package and Phase, in conjunction with SPSS. Ten haplotypes designated in frequency order *1(20.0%) to *10(3.4%) represented 89% of all haplotypes. Haplotype *5 protected against obesity. Haplotype *4 carriers exhibited elevated BP and fat mass, haplotype *6 was associated with raised plasma TG levels. Haplotype *8 also showed similar magnitude effects as *4. These cohort trait analyses and detailed haplotypic analyses enable integration with published case data. Haplotypes *4, *6 and *8 are the only INS VNTR class III-bearing haplotypes, although differing in flanking haplotype, whereas *5 displays unique features in all three genes (with significant commonality with type 1 diabetes-predisposition haplotypes). We propose that long repeat insertion in the insulin gene promoter ('class III'), reported to result in low insulin production, predisposes to the metabolic syndrome features of elevated BP, fat mass or TG level, therefore appearing more frequently in type 2 diabetic, polycystic ovary syndrome and CHD cases. The functional element(s) of *5 for weight-lowering could reside in any of the three genes.
机译:IGF2-INS-TH基因组区域与各种常见疾病有关,包括代谢综合征,2型糖尿病和冠心病(CHD)。在这里,我们介绍了2743位51-62岁男性的详细单倍型分析,涉及体重和组成,血压(BP)和血浆甘油三酸酯(TG)。由于基因座类型输入,缺失数据,多等位基因标记和连续性状表型的数量,使总数据集的使用变得复杂。使用程序单倍型趋势回归,haplo.score,基于进化的单倍型分析程序包和Phase以及SPSS,可以分析数据的不同算法和子集。以* 1(20.0%)至* 10(3.4%)的频率顺序指定的十个单倍型代表了所有单倍型的89%。单倍型* 5可防止肥胖。单倍型* 4携带者表现出升高的BP和脂肪量,单倍型* 6与升高的血浆TG水平相关。单倍型* 8也表现出与* 4类似的幅度效应。这些队列特征分析和详细的单倍型分析可以与已发表的病例数据进行整合。单倍型* 4,* 6和* 8是唯一带有INS VNTR III类的单倍型,尽管侧翼单倍型不同,而* 5在所有三个基因中均表现出独特的特征(与1型糖尿病易感性单​​倍型具有显着共性)。我们建议在胰岛素基因启动子(“ III类”)中长时间重复插入,据报道会导致低胰岛素产生,易导致BP,脂肪量或TG水平升高的代谢综合征特征,因此在2型糖尿病中更常见,多囊卵巢综合征和冠心病病例。 * 5的减肥功能元件可以存在于这三个基因中的任何一个中。

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