Publication: Prognostic value of angiogenic markers in pregnancies with fetal growth restriction
dc.contributor.coauthor | Palmrich P, Pateisky P, Schirwani-Hartl N, Haberl C, Herrmann C, Khalil A, Binder J. | |
dc.contributor.department | School of Medicine | |
dc.contributor.kuauthor | Kalafat, Erkan | |
dc.contributor.schoolcollegeinstitute | SCHOOL OF MEDICINE | |
dc.date.accessioned | 2025-01-19T10:31:52Z | |
dc.date.issued | 2023 | |
dc.description.abstract | Objective Pregnancies with fetal growth restriction (FGR) are at increased risk for pre-eclampsia. Angiogenic markers including soluble fms-like tyrosine kinase-1 (sFlt-1) and placental growth factor (PlGF) are altered in pregnancies complicated by FGR, but their utility for predicting pre-eclampsia in growth-restricted pregnancies is uncertain. This study aimed to evaluate the prognostic value of angiogenic markers for predicting the development of pre-eclampsia in pregnancies with FGR and suspected pre-eclampsia. Methods This was a retrospective study of singleton pregnancies with FGR, defined according to Delphi consensus criteria, which underwent sampling of sFlt-1 and PlGF for suspicion of pre-eclampsia at the Medical University of Vienna, Vienna, Austria, between 2013 and 2020. Women with an established diagnosis of pre-eclampsia at sampling were excluded. Cox regression analysis and logistic regression analysis were performed to evaluate the association of angiogenic markers with the development of pre-eclampsia at various timepoints. Results In this cohort of 93 women, pre-eclampsia was diagnosed in 14 (15.1%) women within 1 week after sampling, 21 (22.6%) within 2 weeks after sampling and 38 (40.9%) at any time after assessment. The sFlt-1/PlGF ratio consistently showed a stronger association with the development of pre-eclampsia compared to sFlt-1 or PlGF alone (pre-eclampsia within 1 week: area under the receiver-operating-characteristics curve, 0.87 vs 0.82 vs 0.72). Models including the sFlt-1/PlGF ratio were associated more strongly with pre-eclampsia hazard compared to models including sFlt-1 or PlGF alone (concordance index, 0.790 vs 0.759 vs 0.755). The risk classification capability of the sFlt-1/PlGF ratio decreased after the 2-week timepoint. The established cut-off value for the sFlt-1/PlGF ratio of < 38 was effective for ruling out pre-eclampsia within 2 weeks, with a negative predictive value of 0.933 and sensitivity of 0.952. Conclusions Use of the sFlt-1/PlGF ratio is preferrable to the use of PlGF alone for the prediction of pre-eclampsia in pregnancies with FGR. Established cut-offs for ruling out the development of pre-eclampsia in the short term seem to be effective in these patients. (c) 2023 The Authors. Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of International Society of Ultrasound in Obstetrics and Gynecology. | |
dc.description.indexedby | WOS | |
dc.description.indexedby | Scopus | |
dc.description.indexedby | PubMed | |
dc.description.issue | 5 | |
dc.description.publisherscope | International | |
dc.description.sponsoredbyTubitakEu | N/A | |
dc.description.volume | 63 | |
dc.identifier.doi | 10.1002/uog.27509 | |
dc.identifier.eissn | 1469-0705 | |
dc.identifier.issn | 0960-7692 | |
dc.identifier.quartile | Q1 | |
dc.identifier.scopus | 2-s2.0-85192056115 | |
dc.identifier.uri | https://doi.org/10.1002/uog.27509 | |
dc.identifier.uri | https://hdl.handle.net/20.500.14288/26309 | |
dc.identifier.wos | 1216321700003 | |
dc.keywords | Adverse maternal outcome | |
dc.keywords | Angiogenic marker | |
dc.keywords | Fetal growth restriction | |
dc.keywords | Placental growth factor | |
dc.keywords | Placental insufficiency | |
dc.keywords | Pre-eclampsia | |
dc.keywords | SFlt-1/PlGF ratio | |
dc.keywords | Soluble fms-like tyrosine kinase-1 | |
dc.language.iso | eng | |
dc.publisher | WILEY | |
dc.relation.ispartof | Ultrasound Obstet Gynecol | |
dc.subject | Medicine | |
dc.title | Prognostic value of angiogenic markers in pregnancies with fetal growth restriction | |
dc.type | Journal Article | |
dspace.entity.type | Publication | |
local.contributor.kuauthor | Kalafat, Erkan | |
local.publication.orgunit1 | SCHOOL OF MEDICINE | |
local.publication.orgunit2 | School of Medicine | |
relation.isOrgUnitOfPublication | d02929e1-2a70-44f0-ae17-7819f587bedd | |
relation.isOrgUnitOfPublication.latestForDiscovery | d02929e1-2a70-44f0-ae17-7819f587bedd | |
relation.isParentOrgUnitOfPublication | 17f2dc8e-6e54-4fa8-b5e0-d6415123a93e | |
relation.isParentOrgUnitOfPublication.latestForDiscovery | 17f2dc8e-6e54-4fa8-b5e0-d6415123a93e |
Files
Original bundle
1 - 1 of 1