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dc.contributorUniv Mayor, Fac Dent, Dept Stat, Chilees
dc.contributor.authorChaparro, Alejandra
dc.contributor.authorMonckeberg, Maximiliano
dc.contributor.authorRealini, Ornella
dc.contributor.authorHernández, Marcela
dc.contributor.authorParam, Fernanda
dc.contributor.authorRamírez, Valeria
dc.contributor.authorKusanovic, Juan
dc.contributor.authorRomero, Roberto
dc.contributor.authorRice, Gregory
dc.contributor.authorIllanes, Sebastian E.
dc.contributor.authorAlbers, Daniela [Univ Mayor, Fac Dent, Dept Stat, Chile]
dc.date.accessioned2023-12-01T20:27:39Z
dc.date.available2023-12-01T20:27:39Z
dc.date.issued2021-05-13
dc.identifier.citationChaparro, A., Monckeberg, M., Realini, O., Hernández, M., Param, F., Albers, D., ... & Illanes, S. E. (2021). Gingival crevicular placental alkaline phosphatase is an early pregnancy biomarker for pre-eclampsia. Diagnostics, 11(4), 661.es
dc.identifier.issneISSN 2075-4418
dc.identifier.otherWOS: 000642976900001
dc.identifier.otherPMID: 33916883
dc.identifier.urihttps://repositorio.umayor.cl/xmlui/handle/sibum/9095
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8067553/pdf/diagnostics-11-00661.pdf
dc.identifier.urihttps://doi.org/10.3390%2Fdiagnostics11040661
dc.identifier.urihttps://digitalcommons.fiu.edu/cgi/viewcontent.cgi?article=1625&context=all_faculty
dc.identifier.urihttps://www.mdpi.com/2075-4418/11/4/661/pdf?version=1617940980
dc.description.abstractEarly and innovative diagnostic strategies are required to predict the risk of developing pre-eclampsia (PE). The purpose of this study was to evaluate the performance of gingival crevicular fluid (GCF) placental alkaline phosphatase (PLAP) concentrations to correctly classify women at risk of PE. A prospectively collected, retrospectively stratified cohort study was conducted, with 412 pregnant women recruited at 11-14 weeks of gestation. Physical, obstetrical, and periodontal data were recorded. GCF and blood samples were collected for PLAP determination by ELISA assay. A multiple logistic regression classification model was developed, and the classification efficiency of the model was established. Within the study cohort, 4.3% of pregnancies developed PE. GCF-PLAP concentration was 3- to 6-fold higher than in plasma samples. GCF-PLAP concentrations and systolic blood pressure were greater in women who developed PE (p = 0.015 and p < 0.001, respectively). The performance of the multiparametric model that combines GCF-PLAP concentration and the levels of systolic blood pressure (at 11-14 weeks gestation) showed an association of systolic blood pressure and GCF-PLAP concentrations with the likelihood of developing PE (OR:1.07; 95% CI 1.01-1.11; p = 0.004 and OR:1.008, 95% CI 1.000-1.015; p = 0.034, respectively). The model had a sensitivity of 83%, a specificity of 72%, and positive and negative predictive values of 12% and 99%, respectively. The area under the receiver operating characteristic (AUC-ROC) curve was 0.77 and correctly classified 72% of PE pregnancies. In conclusion, the multivariate classification model developed may be of utility as an aid in identifying pre-symptomatic women who subsequently develop PE.es
dc.description.sponsorshipThe present study was supported by a Grant (FONDEF IDeA ID16I10452) from the "Fund to Encourage Scientific and Technological Development (FONDEF), Ministry of Education, Government of Chile", Moneda 1375, Santiago de Chile. Dr. Romero was supported, in part, by the Perinatology Research Branch, Division of Obstetrics and Maternal-Fetal Medicine, Division of Intramural Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, U.S. Department of Health and Human Services (NICHD/NIH/DHHS), and, in part, with Federal funds from NICHD/NIH/DHHS under Contract No. HHSN275201300006C.es
dc.format.extent12 p., PDFes
dc.language.isoen_USes
dc.publisherMDPIes
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chilees
dc.titleGingival Crevicular Placental Alkaline Phosphatase Is an Early Pregnancy Biomarker for Pre-Eclampsiaes
dc.typeArtículo o Paperes
umayor.indizadorCOTes
umayor.indexadoWeb of Sciencees
umayor.indexadoPUBMEDes
dc.identifier.doi10.3390/diagnostics11040661
umayor.indicadores.wos-(cuartil)Q2
umayor.indicadores.scopus-(scimago-sjr)SCIMAGO/ INDICE H: 52
umayor.indicadores.scopus-(scimago-sjr)SJR 0,67


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