COMT Val158Met 多态性与非裔美国人和白种人母亲的早发子痫前期显著相关

Melissa R. Kaufman, Amy E. Hwang, Anthony M. Pickrel, Cassandra M. Gray, Kriti M. Goel, David N. Dhanraj, Jerome L. Yaklic, Rose A. Maxwell, Thomas L. Brown
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摘要

本研究旨在评估美国人群中母婴儿茶酚-O-甲基转移酶(COMT)的 Val158Met 多态性。本研究招募了健康对照组、早发先兆子痫患者和晚发先兆子痫患者。通过口腔拭子从母亲和婴儿体内分离出基因组 DNA,并通过四引物扩增 PCR 对 DNA 进行基因分型。我们的研究结果表明,COMT 基因型与晚发型 PE 并无明显关联。虽然非裔美国人和白种人之间没有明显差异,但与 COMTVal158Val 或 COMTVal158Met 相比,非裔美国人和白种人的母体 COMTMet158Met 基因型与早发子痫前期有明显相关性。这些结果表明,母体 COMTMet158Met 基因型可能是早发性子痫前期的一个风险因素。
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The COMT Val158Met Polymorphism is Significantly Associated with Early Onset Preeclampsia in Both African American and Caucasian Mothers
The aim of this study was to evaluate maternal and infant Val158Met polymorphisms of Catechol-O-Methyltransferase (COMT), a reported indicator of preeclamptic risk, in a United States population. Healthy control, early-onset preeclamptic, and late-onset preeclamptic patients were enrolled in this study. Genomic DNA was isolated from mothers and infants via buccal swabs and DNA was genotyped via tetra-primer amplification PCR. Our findings indicate that the COMT genotype was not significantly associated with late-onset PE. While there were no significant differences between African American and Caucasian races, the maternal COMTMet158Met genotype was significantly associated with early-onset preeclampsia in both African Americans and Caucasians when compared to COMTVal158Val or COMTVal158Met. These results suggest that the maternal COMTMet158Met genotype may be a risk factor for early-onset PE.
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