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A multicenter case-control study on screening of single nucleotide polymorphisms in estrogen-metabolizing enzymes and susceptibility to uterine leiomyoma in han chinese

机译:中国汉族人群中雌激素代谢酶单核苷酸多态性筛查及其对子宫平滑肌瘤敏感性的多中心病例对照研究

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摘要

Uterine leiomyoma (UL) is an estrogen-responsive benign tumor in the female reproductive system and the main risk of hysterectomy for women. However, gene polymorphism of estrogen-metabolizing enzymes may lead to the different susceptibility to UL. We detected 10 single mucleotide polymorphisms in three key estrogen metabolite enzymes (COMT, CYP1A1, CYP1B1) in a Chinese Han population consisting of 800 patients and 800 healthy women from five different medical centers. The genetic polymorphism of rs3087869 (IVS1+2329C>T) (OR 3.200, 95% CI 1.614-6.345) and rs4680 (Val158Met) (OR 5.675, 95% CI 2.696-11.942) loci on COMT, rs1048943 (Ile462Val) (OR 4.629, 95% CI 2.216-9.672) and rs4646422 (Gly45Asp) (OR 3.240, 95% CI 1.624-6.461) loci on CYP1A1 and rs1065827 (Ala119Ser) (OR 5.635, 95% CI 2.990-10.619) locus on CYP1B1 were the risk factors to UL development and rs1056836 (Leu432Val) (OR 0.188, 95% CI 0.061-0.575) locus on CYB1B1 may be the protective factor to UL. The results provide a theoretical basis for genetic screening and early intervention to UL-susceptible populations.
机译:子宫平滑肌瘤(UL)是女性生殖系统中雌激素反应性良性肿瘤,是女性子宫切除术的主要风险。但是,雌激素代谢酶的基因多态性可能导致对UL的敏感性不同。我们在中国汉族人群中检测了三种主要雌激素代谢酶(COMT,CYP1A1,CYP1B1)中的10个单核苷酸多态性,该汉族人群由来自五个不同医疗中心的800名患者和800名健康女性组成。 rs3087869(IVS1 + 2329C> T)(OR 3.200,95%CI 1.614-6.345)和rs4680(Val158Met)(OR 5.675,95%CI 2.696-11.942)基因座的遗传多态性,rs1048943(Ile462Val)(OR 4.629) CYP1A1上的95%CI 2.216-9.672)和rs4646422(Gly45Asp)(OR 3.240,95%CI 1.624-6.461)位点和CYP1B1上rs1065827(Ala119Ser)(OR 5.635,95%CI 2.990-10.619)位点是危险因素CYB1B1上的rs1056836(Leu432Val)(OR 0.188,95%CI 0.061-0.575)位点可能是UL的保护因素。该结果为UL易感人群的遗传筛查和早期干预提供了理论基础。

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