Background: Pregnancy-induced hypertension (PIH) is a common cause of perinatal mortality. It is believed to result from the interaction of several factors, including those related to the blood coagulation system. We performed genotyping and subgroup analyses to determine if the 4G/5G genotypes of the plasminogen activator inhibitor-1 gene (
PAI-1) play a role in the pathogenesis of PIH, and to evaluate possible interactions of the
PAI-1 polymorphisms with those of the angiotensinogen gene (
AGT) and the endothelial nitric oxide synthase gene (
NOS3).
Methods: An association study of
PAI-1 polymorphism, and subgroup analyses of common variants of
AGT and
NOS3, among 128 patients with PIH and 376 healthy pregnant controls.
Results: No significant differences were found between the cases and controls in the frequencies of allele 4G or the 4G/4G genotype. In subgroup analyses, after adjustment for multiple comparison, a significant association with the
AGT TT genotype was found among women with the
PAI-1 4G/4G genotype, and an association with the
NOS3 GA+AA genotype was found among women with the 5G/5G or 4G/5G genotypes.
Conclusions: Our findings suggest that there are at least 2 pathways in the pathogenesis of severe PIH. However, with respect to early prediction and prevention of severe PIH, although the
PAI-1 4G/4G genotype alone was not a risk factor for severe PIH, the fact that
PAI-1 genotypes are associated with varying risks for severe PIH suggests that
PAI-1 genotyping of pregnant women, in combination with other tests, may be useful in the development of individualized measures that may prevent severe PIH.
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