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Association of the protein Z intron F G79A gene polymorphism with recurrent pregnancy loss.

机译:蛋白质Z内含子F G79A基因多态性与复发性流产的关联。

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OBJECTIVE: To investigate the association of the common protein Z (PZ) intron F G79A gene polymorphism with recurrent early pregnancy loss (RPL) and its gene-gene interaction with known thrombophilic risk factors for RPL. DESIGN: Case control study. SETTING: University clinic. PATIENT(S): We enrolled 49 women with a history of two consecutive or three to six nonconsecutive pregnancy losses between the 8th and 12th weeks of gestation and 48 age-matched parous controls without a history of pregnancy complications. INTERVENTION(S): None. MAIN OUTCOME MEASURE(S): Allele frequencies of the PZ intron F G79A polymorphism and its gene-gene interaction with known risk factors for RPL. RESULT(S): Fourteen case subjects (28.6%) and 24 control subjects (50.0%) carried at least one A allele. This was associated with a significant reduction of the relative risk for recurrent pregnancy loss (odds ratio [OR] 0.4, 95% confidence interval [CI] 0.2-0.9; adjusted OR 0.3, 95% CI 0.1-0.8). Coexistence of any thrombophilic risk factor studied with the 79A allele resulted in a clear reduction of the primal relative risk for recurrent pregnancy loss. CONCLUSION(S): The isolated presence of the PZ intron F 79A allele as well as the combination with known thrombophilic risk factors was protective against RPL between the 8th and 12th weeks of gestation.
机译:目的:探讨常见蛋白Z(PZ)内含子F G79A基因多态性与复发性早孕丢失(RPL)的关系及其与已知RPL血栓形成危险因素的基因-基因相互作用。设计:病例对照研究。地点:大学诊所。患者:我们纳入了49名在8至12周妊娠期间连续两次或连续3至6次连续性失去妊娠史的妇女以及48名年龄匹配的胎盘对照,没有妊娠并发症的病史。干预措施:无。主要观察指标:PZ内含子F G79A多态性的等位基因频率及其与已知RPL危险因素的基因-基因相互作用。结果:十四名病例受试者(28.6%)和24名对照受试者(50.0%)携带了至少一个A等位基因。这与复发性流产的相对风险的显着降低相关(赔率[OR] 0.4,95%置信区间[CI] 0.2-0.9;调整后的OR 0.3,95%CI 0.1-0.8)。与79A等位基因一起研究的任何血栓形成危险因素的共存可明显降低复发​​性流产的主要相对风险。结论:PZ内含子F 79A等位基因的分离存在以及与已知的血栓形成危险因素的组合在妊娠的第8周和第12周之间对RPL具有保护作用。

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