Association of microsomal epoxide hydrolase gene polymorphism and pre-eclampsia in Turkish women

Aim: To assess the association between human epoxide hydrolase exon 3 and 4 polymorphisms and pre‐eclampsia by carrying out a case‐control study in Turkish women. Methods: DNA was extracted from peripheral blood leukocytes, and genotype distribution of exon 3 and exon 4 of epoxide hydrolase gene (EPHX) was carried out in 271 patients and 155 controls. Results: There was no statistically significant difference in the distribution of genotypes between pre‐eclampsia without HELLP and pre‐eclampsia plus HELLP cases and controls for the exon 3 and 4 polymorphism of EPHX. However, we found a significant association between the predicted enzyme activity level and pre‐eclampsia (P = 0.018). The distribution of subjects with predicted high, intermediate and low microsomal epoxide hydrolase enzyme (EPHX) activity were 23.2, 38.8 and 38% in cases and 12, 47.3 and 40.7% in controls, respectively. Conclusion: Although we could not find any association between genetic variability in exon 3 and 4 of EPHX and pre‐eclampsia, genetic variability in these two exons jointly modifies the predicted enzyme activity and may be a risk factor for pre‐eclampsia.