Key result
MMP-2 polymorphisms (g.-1306C>T and g.-735C>T) did not significantly affect susceptibility to hypertensive disorders of pregnancy or responsiveness to antihypertensive therapy (p > 0.05).
Why the study?
Are MMP-2 polymorphisms (g.-1306C>T and g.-735C>T) associated with susceptibility to hypertensive disorders of pregnancy or responsiveness to antihypertensive therapy?
Observational (n=617)
Are MMP-2 polymorphisms (g.-1306C>T and g.-735C>T) associated with susceptibility to hypertensive disorders of pregnancy or responsiveness to antihypertensive therapy?
MMP-2 polymorphisms (g.-1306C>T and g.-735C>T) do not appear to affect susceptibility to or therapeutic responsiveness in hypertensive disorders of pregnancy.
Should not change clinical management of hypertensive disorders of pregnancy; leaves open MMP-2 relevance pending larger studies.
Imbalanced matrix metalloproteinase (MMP) expression, including MMP-2, has been demonstrated in pre-eclampsia. However, little is known about the effect of polymorphisms in MMP-2 gene on hypertensive disorders of pregnancy. We examined whether two functional MMP-2 polymorphisms (g.-1306C>T and g.-735C>T) are associated with pre-eclampsia and/or gestational hypertension and whether these polymorphisms affect therapeutic responses in women with these conditions. We studied 216 healthy pregnant women (HP), 185 patients with gestational hypertension (GH) and 216 patients with pre-eclampsia (PE). They were stratified as responsive or non-responsive to antihypertensive therapy according to clinical and laboratorial parameters of therapeutic responsiveness. Genomic DNA was extracted from whole blood and genotypes for g-1306C>T and g.-735C>T polymorphisms were determined by real-time PCR using Taqman allele discrimination assays. Haplotype frequencies were inferred using the PHASE 2.1 program. The distributions of MMP-2 genotypes and haplotypes were similar in HP, GH and PE patients (p > 0.05). In addition, we found no significant differences in MMP-2 genotype or haplotype frequencies when GH or PE patients were classified as responsive or non-responsive to antihypertensive therapy (p > 0.05). Our results suggest that MMP-2 polymorphisms do not affect the susceptibility to hypertensive disorders of pregnancy. In parallel, MMP-2 polymorphisms apparently do not affect the responsiveness to antihypertensive therapy of women with these hypertensive disorders of pregnancy.
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Palei et al. (2012) conducted an observational in Hypertensive disorders of pregnancy (n=617). MMP-2 polymorphisms (g.-1306C>T and g.-735C>T) vs. Healthy pregnant women / different genotypes was evaluated on Susceptibility to hypertensive disorders of pregnancy and responsiveness to antihypertensive therapy (p=> 0.05). MMP-2 polymorphisms (g.-1306C>T and g.-735C>T) did not significantly affect susceptibility to hypertensive disorders of pregnancy or responsiveness to antihypertensive therapy (p > 0.05).
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