Association of COMT G675A and MTHFR C677T polymorphisms with hypertensive disorders of pregnancy in Mexican mestizo population

被引:10
|
作者
Vazquez-Alaniz, Fernando [1 ]
Lumbreras-Marquez, Mario I. [1 ]
Sandoval-Carrillo, Ada A. [2 ]
Aguilar-Duran, Marisela [2 ]
Mendez-Hernandez, Edna M. [3 ]
Barraza-Salas, Marcelo [2 ]
Castellanos-Juarez, Francisco X. [2 ]
Salas-Pacheco, Jose M. [2 ]
机构
[1] Secretaria Salud, Hosp Gen Durango, Durango 34000, Mexico
[2] Univ Juarez Estado Durango, Inst Invest Cient, Durango 34000, Mexico
[3] Univ Juarez Estado Durango, Fac Med & Nutr, Durango 34000, Mexico
关键词
Hypertensive disorders of pregnancy; COMT; MTHFR; Polymorphisms; CATECHOL-O-METHYLTRANSFERASE; METHYLENETETRAHYDROFOLATE-REDUCTASE C677T; VAL108/158MET POLYMORPHISM; COMMON MUTATION; BLOOD-PRESSURE; BREAST-CANCER; RISK-FACTOR; PREECLAMPSIA; GENE; SCHIZOPHRENIA;
D O I
10.1016/j.preghy.2013.11.002
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To investigate the relationship between COMT G675A and MTHFR C677T polymorphisms and hypertension disorders of pregnancy (HDP) in a Mexican mestizo population. Design and methods: This case-control study involved 194 HDP and 194 normoevolutive pregnant women. The polymorphisms were genotyped by real time PCR. Results: Our results showed that the COMT AA genotype increases the risk to HDP (OR: 2.67; 95% CI 1.33-5.35), preeclampsia (OR: 2.69; 95% CI 1.00-7.22) and gestational hypertension (OR: 3.87; 95% CI 1.25-12.0). Furthermore, the double mutant genotype (COMTAA/MTHFRTT) potency the risk to HDP more than two times (OR: 5.21; 95% CI 1.12-24.3, p = 0.019). Conclusion: Our work provides evidence that COMT 675AA genotype is a risk factor for HDP and that this risk is increased by the presence of MTHFR 677TT genotype in a Mexican mestizo population. (C) 2013 International Society for the Study of Hypertension in Pregnancy Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:59 / 64
页数:6
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