摘要
This study was undertaken to determine whether the N- acetyl-transferase (NAT) phenotype contributes to the susceptibility for the development of preeclampsia. Study design: The NAT acetylator status was determined by measuring urinary caffeine metabolites in 134 nonpregnant women with a history of preeclampsia and in 109 control women with uncomplicated pregnancy. The χ 2 and logistic regression analyses were used for statistical evaluation of differences in acetylator status. Results: Significantly more fast acetylators were found among the women with a history of preeclampsia (46.3% ) than among the controls (25.4% ). Fast acetylators showed an odds ratio of 2.5 (95% CI 1.4- 4.3) for preeclampsia. No differences in the acetylator status were found between women with a history of preeclampsia only and those with the HELLP syndrome as well. Conclusion: The fast NAT acetylator status, which may result in altered NAT detoxifaction capacity, is associated with preeclampsia.
Objective： This study was undertaken to determine whether the N- acetyl-transferase （NAT） phenotype contributes to the susceptibility for the development of preeclampsia. Study design： The NAT acetylator status was determined by measuring urinary caffeine metabolites in 134 nonpregnant women with a history of preeclampsia and in 109 control women with uncomplicated pregnancy. The X^2 and logistic regression analyses were used for statistical evaluation of differences in acetylator status. Results： Significantly more fast acetylators were found among the women with a history of preeclampsia （46. 3% ） than among the controls （25.4%） . Fast acetylators showed an odds ratio of 2.5 （95% CI 1.4-4.3） for preeclampsia. No differences in the acetylator status were found between women with a history of preeclampsia only and those with the HELLP syndrome as well. Conclusion： The fast NAT acetylator status, which may result in altered NAT detoxifaction capacity, is associated with preeclampsia.
