首页> 中文期刊> 《世界核心医学期刊文摘:妇产科学分册》 >氧化反应相关基因多态性与先兆子痫发病的风险

氧化反应相关基因多态性与先兆子痫发病的风险

         

摘要

Objective: The purpose of this study was to determine whether genetic variability in oxidative stress- related enzymes contributes to individual preeclampsia susceptibility differences. Study Design: Polymorphisms in the cytochrome P450 (CYP)1A1 (MspI), CYP1A1(Ile/Val), glutathione Stransferase (GST)M1, GSTT1, myeloperoxidase (MPO), and manganese superoxide dismutase (MnSOD) genes were evaluated by polymerase chain reaction (PCR) or PCR- restriction fragment length polymorphism (RFLP) in 214 healthy controls with an uncomplicated obstetric history, and in 121 preeclampsia patients. χ 2 analyses were used to statistically evaluate differences. Results: No significant differences in the CYP1A1(MspI) or CYP1A1(Ile/Val) genotypes were observed between the healthy controls and the preeclampsia patients (χ 2 = 1.43, P = 0.49 versus χ 2 = 1.54, P = 0.46). The GSTM1 homozygous null type and GSTT1 homozygous null type were no differences in the patients and controls (χ 2 = 0.01, P = 0.92 versus χ 2 = 0.31, P = 0.57), and no significant differences in the polymorphisms of the MPO and MnSOD genotypes were found between the patients and controls (χ 2 = 2.00, P = 0.37 versus χ 2 = 0.07, P = 0.96). Conclusion: Polymorphisms in the oxidative stress- related genes (CYP1A1, GSTM1, GSTT1, MPO, MnSOD) do not seem to be risk factors for preeclampsia.

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