首页> 外文期刊>Fertility and Sterility: Official Journal of the American Fertility Society, Pacific Coast Fertility Society, and the Canadian Fertility and Andrology Society >Genetic variation in the sex hormone metabolic pathway and endometriosis risk: an evaluation of candidate genes.
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Genetic variation in the sex hormone metabolic pathway and endometriosis risk: an evaluation of candidate genes.

机译:性激素代谢途径的遗传变异和子宫内膜异位症风险:候选基因的评估。

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OBJECTIVE: To evaluate the relationship between common genetic variation in genes involved in the biosynthesis and signaling of estrogen and progesterone and endometriosis risk. DESIGN: Genetic polymorphism analysis. SETTING: Population-based case-control study conducted in Group Health Cooperative enrollees in western Washington. PATIENT(S): Women with newly diagnosed, surgically confirmed endometriosis between 1996 and 2001 (n = 256) and age- and reference year-matched female control subjects without a history of endometriosis (n = 567). INTERVENTIONS(S): None. MAIN OUTCOME MEASURE(S): We evaluated the relationship between common genetic variation and endometriosis risk, using gene-based tests and single-variant analysis of genetic polymorphisms in ESR1, ESR2, PGR, CYP17A1, CYP19A1, HSD17B1, HSD17B2, CYP1A1, CYP1A2, COMT, and GSTM1. RESULT(S): The most consistent gene-based association with endometriosis risk was for CYP19A1. We did not find evidence for consistent significant associations between previously reported candidate SNPs in sex hormone-related genes and endometriosis risk. CONCLUSION(S): In summary, we report increased endometriosis risk with CYP19A1 gene-based tests; replication of the association between endometriosis and this gene or gene region is necessary in a larger study population.
机译:目的:评估生物合成相关基因的常见遗传变异与雌激素和孕激素信号转导及子宫内膜异位症风险之间的关系。设计:遗传多态性分析。地点:在华盛顿州西部的团体卫生合作研究小组中,进行了基于人群的病例对照研究。患者:1996年至2001年间经新诊断,手术确诊为子宫内膜异位的女性(n = 256),以及与年龄和参考年相匹配的女性无内膜异位史的女性(n = 567)。干预措施:无。主要观察指标:我们使用基于基因的测试和ESR1,ESR2,PGR,CYP17A1,CYP19A1,HSD17B1,HSD17B2,CYP1A1,CYP1A2的基因多态性单基因分析,评估了常见遗传变异与子宫内膜异位症风险之间的关系。 ,COMT和GSTM1。结果:基于基因的与子宫内膜异位症风险最一致的关联是CYP19A1。我们没有发现证据表明以前报道的性激素相关基因候选SNP与子宫内膜异位症风险之间存在持续的显着关联。结论:总之,我们报告了基于CYP19A1基因的检测增加了子宫内膜异位症的风险。在较大的研究人群中,子宫内膜异位与该基因或基因区域之间的关联的复制是必要的。

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