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Duarte galactose-1-phosphate uridyl transferase genotypes are not associated with ovarian cancer risk

机译:杜阿尔特半乳糖-1-磷酸尿嘧啶转移酶基因型与卵巢癌风险无关

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Objective: To investigate whether galactose-1-phosphate uridyl transferase (GALT) variant genotypes were associated with epithelial ovarian cancer risk, and to determine if this association was modified by lactose intake. Design: Two prospective cohort studies and a case-control study. Setting: Academic institution. Patient(s): A total of 992 cases and 1,050 population-based control samples from a New England case-control study and 240 cases and 900 control samples from the Nurses' Health Studies. Intervention(s): None. Main Outcome Measure(s): Genotyping of the N314D variant and the 4-bp deletion (-119delGTCA) of GALT with the use of the Taqman 5′ nuclease assay. Duarte1 (D1) genotype individuals have a missense mutation (N314D) associated with normal GALT activity unless it occurs together with an associated 4-bp deletion leading to reduced GALT activity (Duarte2 or D2). Result(s): Logistic regression analysis identified no association between D1/D2 genotypes and ovarian cancer risk (pooled risk ratio 1.1 [95% confidence interval (CI) 0.8-1.5] for D1 and 1.0 [95% CI 0.7-1.4] for D2). We did not observe a significant interaction between D1 and D2 genotypes in analyses stratified by level of lactose intake. Conclusion(s): D1 and D2 genotypes do not appear to play a role in the association between galactose intake, possible ovarian dysfunction, and the link with ovarian cancer.
机译:目的:探讨半乳糖-1-磷酸尿嘧啶转移酶(GALT)变异基因型是否与上皮性卵巢癌风险相关,并确定是否通过摄入乳糖可以改变这种关联。设计:两项前瞻性队列研究和一项病例对照研究。单位:学术机构。患者:一项来自新英格兰病例对照研究的992例病例和1,050个基于人群的对照样本,以及来自护士健康研究的240例病例和900个对照样本。干预措施:无。主要观察指标:使用Taqman 5'核酸酶测定法对N314D变体进行基因分型和GALT的4 bp缺失(-119delGTCA)。 Duarte1(D1)基因型个体具有与正常GALT活性相关的错义突变(N314D),除非它与导致GALT活性降低的相关4 bp缺失一起发生(Duarte2或D2)。结果:Logistic回归分析确定D1 / D2基因型与卵巢癌风险之间没有关联(D1的合并风险比为1.1 [95%置信区间(CI)0.8-1.5],D1的为1.0 [95%CI 0.7-1.4])。 D2)。在按乳糖摄入量分层的分析中,我们没有观察到D1和D2基因型之间的显着相互作用。结论:D1和D2基因型似乎在半乳糖摄入,可能的卵巢功能障碍以及与卵巢癌的联系之间不起作用。

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