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肿瘤坏死因子-α基因多态性与台湾汉族人群子痫前期相关。

Polymorphisms within the Tumor Necrosis Factor-Alpha Gene Is Associated with Preeclampsia in Taiwanese Han Populations.

作者信息

Lin Chih-Wei, Chen Chung-Hwan, Wu Meng-Hsing, Chang Fong-Ming, Kang Lin

机构信息

Department of Obstetrics & Gynecology, College of Medicine, National Cheng Kung University, Tainan 70101, Taiwan.

Department of Obstetrics and Gynecology, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan 70101, Taiwan.

出版信息

Biomedicines. 2023 Mar 11;11(3):862. doi: 10.3390/biomedicines11030862.

Abstract

Preeclampsia (PE) occurs in women pregnant for more than 20 weeks with de novo hypertension and proteinuria, and is a devastating disease in maternal-fetal medicine. Cytokine tumor necrosis factor (TNF)-α may play a key role in the pathogenesis of PE. We conducted this study to investigate the regulatory regions of the TNF genes, by investigating two promoter polymorphisms, TNFA-308G/A (rs1800629) and -238G/A (rs361525), known to influence TNF expression, and their relationship to PE. An observational, monocentric, case-control study was conducted. We retrospectively collected 74 cases of severe PE and 119 pregnant women without PE as control. Polymerase chain reaction (PCR) was carried out for allele analysis. Higher A allele in women with PE was found in rs1800629 but not rs361525. In this study, we first found that polymorphism at the position -308, but not -238, in the promoter region of the TNF-α gene can contribute to severe PE in Taiwanese Han populations. The results of our study are totally different to previous Iranian studies, but have some similarity to a previous UK study. Further studies are required to confirm the roles of rs1800629 and rs361525 in PE with circulating TNF-α in PE.

摘要

子痫前期(PE)发生于妊娠20周以上的孕妇,伴有新发高血压和蛋白尿,是母婴医学中一种严重的疾病。细胞因子肿瘤坏死因子(TNF)-α可能在PE的发病机制中起关键作用。我们开展这项研究,通过调查已知会影响TNF表达的两个启动子多态性,即TNFA-308G/A(rs1800629)和-238G/A(rs361525),来研究TNF基因的调控区域及其与PE的关系。进行了一项观察性、单中心病例对照研究。我们回顾性收集了74例重度PE患者和119例无PE的孕妇作为对照。采用聚合酶链反应(PCR)进行等位基因分析。在rs1800629中发现PE患者的A等位基因频率较高,但在rs361525中未发现。在本研究中,我们首次发现,在台湾汉族人群中,TNF-α基因启动子区域-308位点的多态性而非-238位点的多态性可能与重度PE有关。我们的研究结果与之前伊朗的研究完全不同,但与之前英国的一项研究有一些相似之处。需要进一步研究来证实rs1800629和rs361525在PE伴循环TNF-α中的作用。

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