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B 淋巴细胞刺激因子基因(BLyS)启动子-817C>T 变异与巴西人群子宫内膜异位症相关不孕和特发性不孕的易感性。

Promoter -817C>T variant of B lymphocyte stimulator gene (BLyS) and susceptibility to endometriosis-related infertility and idiopathic infertility in Brazilian population.

机构信息

Division of Human Reproduction and Genetics, Department of Gynaecology and Obstetrics, Faculdade de Medicina do ABC, Santo André/SP, Brazil.

出版信息

Scand J Immunol. 2011 Dec;74(6):628-31. doi: 10.1111/j.1365-3083.2011.02616.x.

Abstract

Many theories have been proposed to explain the development of endometriosis, and recently, autoimmune aetiology has been suggested. Besides, it is well known that endometriosis, especially the advanced disease, may impair fertility. B lymphocyte stimulator (BLyS) is a cytokine produced by macrophages and is necessary for normal B cell development. One of the most studied polymorphisms is the -817C/T in the promoter region of the gene. We aimed to assess the association between endometriosis-related infertility and idiopathic infertility and the BLyS -817C/T polymorphism in a Brazilian population. We performed a case-control study comprising 165 infertile women with endometriosis, 83 with idiopathic infertility and 145 fertile and assessed the association with BLys -817C/T polymorphism. BLyS -817C/T polymorphism was detected using TaqMan PCR. The results were analysed statistically, and a P-value < 0.05 was considered significant. The results disclosed similar genotype and allelic frequencies between endometriosis-related infertility (P = 0.225) and control group, regardless of the disease stage (P = 0.213 and P = 0.462, respectively). However, a statistically significant difference was observed regarding idiopathic infertile group (P = 0.048) compared with controls. Considering the dominant and recessive inheritance models, no significant differences in both endometriosis and idiopathic infertility group were found. The genotype frequencies were in Hardy-Weinberg equilibrium in all studied groups. The results point to a possible association between BLyS -817C/T polymorphism and idiopathic infertility in Brazilian population.

摘要

许多理论被提出以解释子宫内膜异位症的发展,最近,自身免疫病因学也被提出。此外,众所周知,子宫内膜异位症,特别是晚期疾病,可能会损害生育能力。B 淋巴细胞刺激因子 (BLyS) 是一种由巨噬细胞产生的细胞因子,是正常 B 细胞发育所必需的。研究最多的多态性之一是基因启动子区域的 -817C/T。我们旨在评估巴西人群中子宫内膜异位症相关不孕和特发性不孕与 BLyS-817C/T 多态性之间的关联。我们进行了一项病例对照研究,包括 165 名患有子宫内膜异位症的不孕妇女、83 名患有特发性不孕的妇女和 145 名生育能力正常的妇女,并评估了与 BLyS-817C/T 多态性的关联。使用 TaqMan PCR 检测 BLyS-817C/T 多态性。对结果进行统计学分析,P 值 < 0.05 被认为具有统计学意义。结果显示,无论疾病阶段如何,子宫内膜异位症相关不孕组(P = 0.225)与对照组的基因型和等位基因频率相似。然而,与对照组相比,特发性不孕组的差异具有统计学意义(P = 0.048)。考虑到显性和隐性遗传模型,在子宫内膜异位症和特发性不孕组中均未发现显著差异。在所有研究组中,基因型频率均处于哈迪-温伯格平衡状态。结果表明,BLyS-817C/T 多态性与巴西人群中的特发性不孕可能存在关联。

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