The genetics of endometriosis.

S. Kennedy
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引用次数: 17

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.
子宫内膜异位症的遗传学。
子宫内膜异位症可能是一种复杂的特征,就像糖尿病、高血压或哮喘一样,这意味着这种疾病是由多种基因和环境之间的相互作用引起的。本文回顾了在人类和非人类灵长类动物中支持子宫内膜异位症遗传基础理论的证据。OXEGENE研究,旨在通过连锁分析确定子宫内膜异位症的易感基因,也被描述。目前正在从至少有两个姐妹的家庭中收集DNA,这些姐妹经外科手术证实患有美国生育学会修订的III期和IV期疾病,以进行全基因组的易感基因搜索。参与半乳糖代谢和二恶英解毒的候选基因也正在分析中。确定子宫内膜异位症易感性的基因可能会导致对疾病病因的更好理解,并及时改进治疗策略和诊断方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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