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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/12235
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dc.contributor.authorSibai, Baha M.-
dc.contributor.authorKoch, Matthew A.-
dc.contributor.authorFreire, Salvio-
dc.contributor.authorPinto e Silva, Joao Luiz-
dc.contributor.authorRudge, Marilza Vieira Cunha-
dc.contributor.authorMartins-Costa, Sergio-
dc.contributor.authorBartz, Janet-
dc.contributor.authorSantos, Cleide de Barros-
dc.contributor.authorCecatti, Jose Guilherme-
dc.contributor.authorCosta, Roberto-
dc.contributor.authorRamos, Jose Geraldo-
dc.contributor.authorSpinnato, Joseph A.-
dc.date.accessioned2014-05-20T13:35:32Z-
dc.date.accessioned2016-10-25T16:52:56Z-
dc.date.available2014-05-20T13:35:32Z-
dc.date.available2016-10-25T16:52:56Z-
dc.date.issued2008-09-01-
dc.identifierhttp://dx.doi.org/10.1016/j.ajog.2008.06.071-
dc.identifier.citationAmerican Journal of Obstetrics and Gynecology. New York: Mosby-elsevier, v. 199, n. 3, p. 9, 2008.-
dc.identifier.issn0002-9378-
dc.identifier.urihttp://hdl.handle.net/11449/12235-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/12235-
dc.description.abstractOBJECTIVE: Our objective was to determine whether measurement of placenta growth factor (PLGF), inhibin A, or soluble fms-like tyrosine kinase-1 (sFlt-1) at 2 times during pregnancy would usefully predict subsequent preeclampsia ( PE) in women at high risk. STUDY DESIGN: We analyzed serum obtained at enrollment (12(0/7) to 19(6/7) weeks) and follow-up (24-28 weeks) from 704 patients with previous PE and/or chronic hypertension (CHTN) enrolled in a randomized trial for the prevention of PE. Logistic regression analysis assessed the association of log-transformed markers with subsequent PE; receiver operating characteristic analysis assessed predictive value. RESULTS: One hundred four developed preeclampsia: 27 at 37 weeks or longer and 77 at less than 37 weeks (9 at less than 27 weeks). None of the markers was associated with PE at 37 weeks or longer. Significant associations were observed between PE at less than 37 weeks and reduced PLGF levels at baseline (P =.022) and follow-up (P <.0001) and elevated inhibin A (P <.0001) and sFlt-1 (P =.0002) levels at follow-up; at 75% specificity, sensitivities ranged from 38% to 52%. Using changes in markers from baseline to follow-up, sensitivities were 52-55%. Associations were observed between baseline markers and PE less than 27 weeks (P <=.0004 for all); sensitivities were 67-89%, but positive predictive values (PPVs) were only 3.4-4.5%. CONCLUSION: Inhibin A and circulating angiogenic factors levels obtained at 12(0/7) to 19(6/7) weeks have significant associations with onset of PE at less than 27 weeks, as do levels obtained at 24-28 weeks with onset of PE at less than 37 weeks. However, because the corresponding sensitivities and/or PPVs were low, these markers might not be clinically useful to predict PE in women with previous PE and/or CHTN.en
dc.format.extent9-
dc.language.isoeng-
dc.publisherMosby-elsevier-
dc.sourceWeb of Science-
dc.subjectinhibin Aen
dc.subjectPLGFen
dc.subjectpreeclampsiaen
dc.subjectsFlt-1en
dc.titleSerum inhibin A and angiogenic factor levels in pregnancies with previous preeclampsia and/or chronic hypertension: are they useful markers for prediction of subsequent preeclampsia?en
dc.typeoutro-
dc.contributor.institutionUniv Cincinnati-
dc.contributor.institutionRTI Int-
dc.contributor.institutionUniversidade Federal de Pernambuco (UFPE)-
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade Federal do Rio Grande do Sul (UFRGS)-
dc.description.affiliationUniv Cincinnati, Coll Med, Cincinnati, OH 45221 USA-
dc.description.affiliationRTI Int, Res Triangle Pk, NC USA-
dc.description.affiliationUniversidade Federal de Pernambuco (UFPE), Hosp Clin, Recife, PE, Brazil-
dc.description.affiliationUniv Estadual Campinas, Campinas, SP, Brazil-
dc.description.affiliationUniv Estadual Paulista, Botucatu, SP, Brazil-
dc.description.affiliationUniversidade Federal do Rio Grande do Sul (UFRGS), Hosp Clin, Porto Alegre, RS, Brazil-
dc.description.affiliationUnespUniv Estadual Paulista, Botucatu, SP, Brazil-
dc.identifier.doi10.1016/j.ajog.2008.06.071-
dc.identifier.wosWOS:000258955400020-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofAmerican Journal of Obstetrics and Gynecology-
dc.identifier.orcid0000-0002-9227-832X-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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