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首页> 外文期刊>Scandinavian journal of immunology. >TGFB1 Functional Gene Polymorphisms (C-509T and T869C) in the Maternal Susceptibility to Pre-eclampsia in South Indian Women
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TGFB1 Functional Gene Polymorphisms (C-509T and T869C) in the Maternal Susceptibility to Pre-eclampsia in South Indian Women

机译:TGFB1功能基因多态性(C-509T和T869C)在南印度妇女的子痫前期母体易感性中。

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Pre-eclampsia (PE), a pregnancy-specific vascular disorder characterized by hypertension and proteinuria, is hypothesized to be the result of inadequate placental angiogenesis with attendant systemic inflammation. The pleiotropic cytokine, Transforming Growth Factor-1 (TGF-1), is considered to be a key candidate gene in the molecular pathogenesis of PE by virtue of its ability to not only regulate angiogenesis and apoptosis of target cells, but also by acting as a master controller of Th1/Th2 cytokine balance and production of the anti-inflammatory peripheral regulatory T cells (FOXP3+ Tregs). Based on this presumption, we screened a total of 469 pregnant women from South India that include 239 patients with PE and 230 healthy controls for the two functional polymorphisms of TGFB1 gene (C-509T and T869C). The genotype frequencies of these two polymorphisms differed significantly between the PE and control groups (P=0.01 and P=0.002, for the TGFB1 C-509T and T869C polymorphisms, respectively). Under the over-dominant model, the CT genotype of the TGFB1 C509T polymorphism showed a high protective effect (P=3e-04), while the TT genotype of the same variant appeared to be the predisposing genotype (P=0.003). The T-T and C-C haplotypes were found to be the risk haplotypes blocks towards PE (OR=4.72; P=0.031, OR=5.39; P=0.03), respectively. Strong linkage disequilibrium was seen between the two polymorphisms. Our investigations revealed a significant influence of TGFB1 C-509T and T869C polymorphisms on the PE risk in South Indian women. The study represents one of the first of its kind from the Indian subcontinent.
机译:子痫前期(PE)是一种以高血压和蛋白尿为特征的妊娠特异性血管疾病,被认为是胎盘血管生成不足并伴有全身性炎症的结果。多效细胞因子转化生长因子-1(TGF-1)被认为是PE分子发病机制中的关键候选基因,因为它不仅具有调节靶细胞的血管生成和凋亡的能力,而且还具有以下作用: Th1 / Th2细胞因子平衡和抗炎性外周调节性T细胞(FOXP3 + Tregs)产生的主要控制者。基于此假设,我们筛查了来自印度南部的469名孕妇,其中包括239名PE患者和230名健康对照者的TGFB1基因的两个功能多态性(C-509T和T869C)。 PE和对照组之间这两个多态性的基因型频率有显着差异(对于TGFB1 C-509T和T869C多态性,分别为P = 0.01和P = 0.002)。在占主导地位的模型下,TGFB1 C509T多态性的CT基因型显示出高保护作用(P = 3e-04),而同一变体的TT基因型似乎是易感基因型(P = 0.003)。发现T-T和C-C单倍型分别是对PE的危险单倍型阻滞(OR = 4.72; P = 0.031,OR = 5.39; P = 0.03)。在两个多态性之间观察到强烈的连锁不平衡。我们的调查显示,TGFB1 C-509T和T869C多态性对南印度妇女的PE风险有重大影响。该研究是印度次大陆同类研究中的第一项。

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