Kim Young Ju, Park Hye Sook, Park Mi Hye, Suh Suk Hyo, Pang Myung-Geol
Department of Obstetrics and Gynecology, Ewha Womans University, 911-1 MokDong Yangcheonku, Seoul 151-070, Korea.
Eur J Obstet Gynecol Reprod Biol. 2005 Mar 1;119(1):42-6. doi: 10.1016/j.ejogrb.2004.06.009.
The purpose of this study was to determine whether genetic variability in oxidative stress-related enzymes contributes to individual preeclampsia susceptibility differences.
Polymorphisms in the cytochrome P450 (CYP)1A1 (MspI), CYP1A1(Ile/Val), glutathione S-transferase (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. Chi2 analyses were used to statistically evaluate differences.
No significant differences in the CYP1A1(MspI) or CYP1A1(Ile/Val) genotypes were observed between the healthy controls and the preeclampsia patients (chi2 = 1.43, P = 0.49 versus chi2 = 1.54, P = 0.46). The GSTM1 homozygous null type and GSTT1 homozygous null type were no differences in the patients and controls (chi2 = 0.01, P = 0.92 versus chi(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 (chi2 = 2.00, P = 0.37 versus chi2 = 0.07, P = 0.96).
Polymorphisms in the oxidative stress-related genes (CYP1A1, GSTM1, GSTT1, MPO, MnSOD) do not seem to be risk factors for preeclampsia.
本研究旨在确定氧化应激相关酶的基因变异是否导致个体子痫前期易感性差异。
采用聚合酶链反应(PCR)或PCR-限制性片段长度多态性(RFLP)方法,对214例无复杂产科病史的健康对照者和121例子痫前期患者的细胞色素P450(CYP)1A1(MspI)、CYP1A1(Ile/Val)、谷胱甘肽S-转移酶(GST)M1、GSTT1、髓过氧化物酶(MPO)和锰超氧化物歧化酶(MnSOD)基因多态性进行评估。采用卡方分析进行统计学差异评估。
健康对照者与子痫前期患者之间,未观察到CYP1A1(MspI)或CYP1A1(Ile/Val)基因型存在显著差异(卡方=1.43,P=0.49;对比卡方=1.54,P=0.46)。患者与对照者之间,GSTM1纯合无效型和GSTT1纯合无效型无差异(卡方=0.01,P=0.92;对比卡方=0.31,P=0.57),患者与对照者之间,MPO和MnSOD基因型多态性也未发现显著差异(卡方=2.00,P=0.37;对比卡方=0.07,P=0.96)。
氧化应激相关基因(CYP1A1、GSTM1、GSTT1、MPO、MnSOD)的多态性似乎不是子痫前期的危险因素。