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与子宫内膜异位症相关的新候选基因。

New candidate genes associated to endometriosis.

作者信息

Christofolini Denise Maria, Mafra Fernanda Abani, Catto Michelle Cristina, Bianco Bianca, Barbosa Caio Parente

机构信息

a Instituto Ideia Fértil de Saúde Reprodutiva , Santo André , Brazil.

b Discipline of Sexual and Reproductive Health and Populational Genetics, Department of Collective Health , Faculdade de Medicina do ABC , Santo André , Brazil.

出版信息

Gynecol Endocrinol. 2019 Jan;35(1):62-65. doi: 10.1080/09513590.2018.1499090. Epub 2018 Jul 25.

Abstract

A previous GWAS study performed on Brazilian pooled samples indicated some SNPs (single nucleotide polymorphisms) differentially frequent in infertile patients with endometriosis and controls. Some of them were located in the genes whose biological function suggests that they could be associated with endometriosis pathogenesis; thus, the purpose here was to confirm GWAS findings in a larger group of cases and controls in order to associate the results with the pathogenesis of endometriosis. Then, a genetic association study comprising 394 infertile women with endometriosis and 650 fertile control women was conducted. TaqMan allelic discrimination assays were used to investigate the frequency of three SNPs in the genes KAZN (rs10928050), LAMA5 (rs2427284), and TAC3 (rs733629). The analysis revealed a significant association of KAZN rs10928050 (p = .015) and LAMA5 rs2427284 (p = .0059) SNPs with endometriosis-related infertility, while TAC3 rs733629 showed no difference between cases and controls. As a conclusion, it was possible to observe that individual genotyping of a larger sample of patients and controls confirmed the association among KAZN and LAMA5 with endometriosis-related infertility and revealed new candidate genes contributing to the condition.

摘要

一项先前针对巴西混合样本进行的全基因组关联研究(GWAS)表明,某些单核苷酸多态性(SNP)在患有子宫内膜异位症的不孕患者和对照组中的出现频率存在差异。其中一些位于某些基因中,这些基因的生物学功能表明它们可能与子宫内膜异位症的发病机制有关;因此,本研究的目的是在更大规模的病例组和对照组中证实GWAS的研究结果,以便将结果与子宫内膜异位症的发病机制联系起来。然后,开展了一项基因关联研究,纳入了394名患有子宫内膜异位症的不孕女性和650名可育对照女性。采用TaqMan等位基因鉴别分析方法来研究KAZN基因(rs10928050)、LAMA5基因(rs2427284)和TAC3基因(rs733629)中三个SNP的频率。分析显示,KAZN基因的rs10928050(p = 0.015)和LAMA5基因的rs2427284(p = 0.0059)与子宫内膜异位症相关不孕存在显著关联,而TAC3基因的rs733629在病例组和对照组之间未显示出差异。总之,可以观察到,对更大样本的患者和对照组进行个体基因分型证实了KAZN和LAMA5与子宫内膜异位症相关不孕之间的关联,并揭示了导致该病的新候选基因。

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