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子宫内膜异位症的遗传学

The genetics of endometriosis.

作者信息

Kennedy S

机构信息

Nuffield Department of Obstetrics and Gynaecology, University of Oxford, England.

出版信息

J Reprod Med. 1998 Mar;43(3 Suppl):263-8.

PMID:9564659
Abstract

Endometriosis is probably a complex trait, like diabetes, hypertension or asthma, which implies that the disease is caused by an interaction between multiple genes and the environment. This paper reviews the evidence, in both human and nonhuman primates, that supports the theory of a genetic basis to endometriosis. The OXEGENE study, which aims to identify susceptibility genes in endometriosis through linkage analysis, is also described. DNA is being collected from families containing at least two sisters with surgically confirmed revised American Fertility Society stage III and IV disease to carry out a genome-wide search for susceptibility genes. Candidate genes involved in galactose metabolism and dioxin detoxification are also being analyzed. The identification of genes conferring susceptibility to endometriosis may lead to a better understanding of disease etiology and, in time, improved therapeutic strategies and diagnostic methods.

摘要

子宫内膜异位症可能是一种复杂性状,类似于糖尿病、高血压或哮喘,这意味着该疾病是由多个基因与环境之间的相互作用所引起的。本文综述了人类和非人类灵长类动物中支持子宫内膜异位症存在遗传基础这一理论的证据。文中还描述了旨在通过连锁分析确定子宫内膜异位症易感基因的OXEGENE研究。正在从至少有两名经手术确诊为美国生殖医学学会修订版III期和IV期疾病的姐妹的家庭中收集DNA,以进行全基因组范围内的易感基因搜索。参与半乳糖代谢和二噁英解毒的候选基因也在进行分析。确定赋予子宫内膜异位症易感性的基因可能会使我们更好地理解疾病病因,并最终改进治疗策略和诊断方法。

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