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肿瘤坏死因子-α基因单倍型与子痫前期有关。

Tumour necrosis factor-alpha gene haplotype is associated with pre-eclampsia.

作者信息

Saarela Tanja, Hiltunen Mikko, Helisalmi Seppo, Heinonen Seppo, Laakso Markku

机构信息

Department of Obstetrics and Gynaecology, University of Kuopio, Kuopio, Finland.

出版信息

Mol Hum Reprod. 2005 Jun;11(6):437-40. doi: 10.1093/molehr/gah182. Epub 2005 May 18.

Abstract

We determined whether polymorphisms in the promoter region of the tumour necrosis factor alpha (TNF-alpha) gene contributes to differences in susceptibility to develop pre-eclampsia. The study involved 133 pre-eclamptic and 115 healthy pregnant women who were genotyped for the G-308A polymorphism of the TNF-alpha gene. The frequency of the G-308A allele was more common in the pre-eclampsia group than among the controls (P=0.046), giving an odds ratio of 0.57 (95% CI: 0.32-0.99), but there were no differences in the genotype distribution. The data from the G-308A polymorphism was combined with the previously published genotype and allele data from the C-850T polymorphism of the TNF-alpha gene, and used to assess a haplotype estimation analysis. Estimated overall pair of loci haplotype frequencies differed significantly between the groups (P=0.023+/-0.004). In the single haplotype association analysis, the haplotype C-A versus others was over-represented in the pre-eclampsia group (P=0.041+/-0.003), whereas the haplotype T-G versus others was less common in the pre-eclampsia group (P=0.035+/-0.003), compared with the controls. In conclusion, the polymorphisms of the TNF-alpha gene showed a significant haplotype association with susceptibility to pre-eclampsia in the Finnish population.

摘要

我们确定肿瘤坏死因子α(TNF-α)基因启动子区域的多态性是否会导致子痫前期易感性的差异。该研究纳入了133例子痫前期孕妇和115例健康孕妇,对她们进行了TNF-α基因G-308A多态性的基因分型。G-308A等位基因的频率在子痫前期组中比对照组更常见(P = 0.046),优势比为0.57(95%可信区间:0.32 - 0.99),但基因型分布没有差异。将G-308A多态性的数据与先前发表的TNF-α基因C-850T多态性的基因型和等位基因数据相结合,并用于评估单倍型估计分析。两组之间估计的总体位点对单倍型频率存在显著差异(P = 0.023±0.004)。在单倍型关联分析中,与其他单倍型相比,单倍型C-A在子痫前期组中过度表达(P = 0.041±0.003),而与对照组相比,单倍型T-G在子痫前期组中较少见(P = 0.035±0.003)。总之,在芬兰人群中,TNF-α基因的多态性与子痫前期易感性存在显著的单倍型关联。

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