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dc.contributor.authorMoore Simas, Tiffany A.
dc.contributor.authorCrawford, Sybil L.
dc.contributor.authorSolitro, Matthew J.
dc.contributor.authorFrost, Sara C.
dc.contributor.authorMeyer, Bruce A.
dc.contributor.authorMaynard, Sharon E.
dc.date2022-08-11T08:11:05.000
dc.date.accessioned2022-08-23T17:32:25Z
dc.date.available2022-08-23T17:32:25Z
dc.date.issued2007-09-01
dc.date.submitted2010-03-01
dc.identifier.citationAm J Obstet Gynecol. 2007 Sep;197(3):244.e1-8. <a href="http://dx.doi.org/10.1016/j.ajog.2007.06.030">Link to article on publisher's site</a>
dc.identifier.issn0002-9378 (Linking)
dc.identifier.doi10.1016/j.ajog.2007.06.030
dc.identifier.pmid17826405
dc.identifier.urihttp://hdl.handle.net/20.500.14038/50947
dc.description.abstractOBJECTIVE: The objective of the study was to evaluate angiogenic factors for the prediction of preeclampsia in high-risk women. STUDY DESIGN: We collected serial serum specimens from 94 women at high preeclampsia risk between 22 and 36 weeks' gestation. Soluble fms-like tyrosine kinase-1 (sFlt1) and placental growth factor (PlGF) were measured by enzyme-linked immunosorbent assay. RESULTS: Mean serum sFlt1 and the sFlt1/PlGF ratio were higher in subjects who developed early-onset (less than 34 weeks) preeclampsia, as compared with subjects without preeclampsia, from 22 weeks gestation onward. In subjects who developed late-onset (34 weeks or later) preeclampsia, sFlt1 was significantly increased after 31 weeks' gestation. The sFlt1/PlGF ratio at 22-26 weeks was highly predictive of early-onset preeclampsia. The within-woman rate of change of the sFlt1/PlGF ratio was predictive of overall preeclampsia risk. CONCLUSIONS: In high-risk women, serum sFlt1 and the sFlt1:PlGF ratio are altered prior to preeclampsia onset and may be predictive of preeclampsia. Larger studies are needed to confirm these findings.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=17826405&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1016/j.ajog.2007.06.030
dc.subjectAdult
dc.subjectAngiogenesis Inducing Agents
dc.subjectBiological Markers
dc.subjectFemale
dc.subjectHumans
dc.subjectPre-Eclampsia
dc.subjectPredictive Value of Tests
dc.subjectPregnancy
dc.subjectPregnancy Proteins
dc.subjectPregnancy, High-Risk
dc.subjectProspective Studies
dc.subjectVascular Endothelial Growth Factor Receptor-1
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.subjectObstetrics and Gynecology
dc.titleAngiogenic factors for the prediction of preeclampsia in high-risk women
dc.typeJournal Article
dc.source.journaltitleAmerican journal of obstetrics and gynecology
dc.source.volume197
dc.source.issue3
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/wfc_pp/477
dc.identifier.contextkey1182214
html.description.abstract<p>OBJECTIVE: The objective of the study was to evaluate angiogenic factors for the prediction of preeclampsia in high-risk women.</p> <p>STUDY DESIGN: We collected serial serum specimens from 94 women at high preeclampsia risk between 22 and 36 weeks' gestation. Soluble fms-like tyrosine kinase-1 (sFlt1) and placental growth factor (PlGF) were measured by enzyme-linked immunosorbent assay.</p> <p>RESULTS: Mean serum sFlt1 and the sFlt1/PlGF ratio were higher in subjects who developed early-onset (less than 34 weeks) preeclampsia, as compared with subjects without preeclampsia, from 22 weeks gestation onward. In subjects who developed late-onset (34 weeks or later) preeclampsia, sFlt1 was significantly increased after 31 weeks' gestation. The sFlt1/PlGF ratio at 22-26 weeks was highly predictive of early-onset preeclampsia. The within-woman rate of change of the sFlt1/PlGF ratio was predictive of overall preeclampsia risk.</p> <p>CONCLUSIONS: In high-risk women, serum sFlt1 and the sFlt1:PlGF ratio are altered prior to preeclampsia onset and may be predictive of preeclampsia. Larger studies are needed to confirm these findings.</p>
dc.identifier.submissionpathwfc_pp/477
dc.contributor.departmentDepartment of Obstetrics and Gynecology
dc.contributor.departmentDepartment of Medicine, Division of Preventive and Behavioral Medicine
dc.source.pages244.e1-8


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