Publicação:
Tissue inhibitor of matrix metalloproteinase-1 polymorphism, plasma TIMP-1 levels, and antihypertensive therapy responsiveness in hypertensive disorders of pregnancy

dc.contributor.authorLuizon, M. R.
dc.contributor.authorPalei, A. C. T.
dc.contributor.authorSandrim, Valéria Cristina [UNESP]
dc.contributor.authorAmaral, L. M.
dc.contributor.authorMachado, J. S. R.
dc.contributor.authorLacchini, R.
dc.contributor.authorCavalli, R. C.
dc.contributor.authorDuarte, G.
dc.contributor.authorTanus-Santos, J. E.
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniv Mississippi
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2015-03-18T15:54:16Z
dc.date.available2015-03-18T15:54:16Z
dc.date.issued2014-12-01
dc.description.abstractTissue inhibitor of metalloproteinase (TIMP)-1 is a major endogenous inhibitor of matrix metalloproteinase (MMP)-9, which may affect the responsiveness to therapy in hypertensive disorders of pregnancy. We examined whether TIMP-1 polymorphism (g.-9830T>G, rs2070584) modifies plasma MMP-9 and TIMP-1 levels and the response to antihypertensive therapy in 596 pregnant: 206 patients with preeclampsia (PE), 183 patients with gestational hypertension (GH) and 207 healthy pregnant controls. We also studied the TIMP-3 polymorphism (g.-1296T>C, rs9619311). Plasma MMP-9 and TIMP-1 levels were measured by ELISA. GH patients with the GG genotype for the TIMP-1 polymorphism had lower MMP-9 levels and MMP-9/TIMP-1 ratios than those with the TT genotype. PE patients with the TG genotype had higher TIMP-1 levels. The G allele and the GG genotype were associated with PE and responsiveness to antihypertensive therapy in PE, but not in GH. Our results suggest that the TIMP-1 g.-9830T>G polymorphism not only promotes PE but also decreases the responses to antihypertensive therapy.en
dc.description.affiliationUniv Sao Paulo, Ribeirao Preto Med Sch, Dept Pharmacol, BR-14049900 Sao Paulo, Brazil
dc.description.affiliationUniv Mississippi, Med Ctr, Dept Physiol & Biophys, Jackson, MS 39216 USA
dc.description.affiliationUniv Estadual Paulista UNESP, Inst Biosci, Dept Pharmacol, Sao Paulo, Brazil
dc.description.affiliationUniv Sao Paulo, Ribeirao Preto Med Sch, Dept Gynecol & Obstet, BR-14049900 Sao Paulo, Brazil
dc.description.affiliationUnespUniv Estadual Paulista UNESP, Inst Biosci, Dept Pharmacol, Sao Paulo, Brazil
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.format.extent535-541
dc.identifierhttp://dx.doi.org/10.1038/tpj.2014.26
dc.identifier.citationPharmacogenomics Journal. London: Nature Publishing Group, v. 14, n. 6, p. 535-541, 2014.
dc.identifier.doi10.1038/tpj.2014.26
dc.identifier.issn1470-269X
dc.identifier.urihttp://hdl.handle.net/11449/116850
dc.identifier.wosWOS:000345495200006
dc.language.isoeng
dc.publisherNature Publishing Group
dc.relation.ispartofPharmacogenomics Journal
dc.relation.ispartofjcr3.812
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.titleTissue inhibitor of matrix metalloproteinase-1 polymorphism, plasma TIMP-1 levels, and antihypertensive therapy responsiveness in hypertensive disorders of pregnancyen
dc.typeArtigo
dcterms.rightsHolderNature Publishing Group
dspace.entity.typePublication
unesp.author.orcid0000-0002-6168-7470[3]
unesp.author.orcid0000-0002-5363-634X[5]
unesp.author.orcid0000-0002-3738-2036[6]
unesp.author.orcid0000-0002-8331-3525[1]
unesp.author.orcid0000-0001-5010-4914[7]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Botucatupt
unesp.departmentFarmacologia - IBBpt

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