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dc.contributor.authorVelásquez Penagos, Jesús Arnulfo-
dc.contributor.authorBurwick, Richard-
dc.contributor.authorValencia, Catalina-
dc.contributor.authorVargas Rodríguez, Johanna Celina-
dc.contributor.authorSilva, Jaime-
dc.contributor.authorEdna Estrada, Francisco-
dc.contributor.authorGutiérrez Marín, Jorge Hernán-
dc.contributor.authorTrujillo Otálvaro, Juliana Marcela-
dc.contributor.authorGómez, Ana-
dc.contributor.authorRincón, Mónica-
dc.contributor.authorCabas, Carlos-
dc.contributor.authorQuintero, Álvaro-
dc.contributor.authorGonzález, Nataly-
dc.contributor.authorLenis Ballesteros, Viviana-
dc.contributor.authorTolosa Ardila, Jorge Enrique-
dc.date.accessioned2023-11-11T03:03:39Z-
dc.date.available2023-11-11T03:03:39Z-
dc.date.issued2018-
dc.identifier.issn0002-9378-
dc.identifier.urihttps://hdl.handle.net/10495/37235-
dc.description.abstractABSTRACT: Objective Complement activation occurs in normal pregnancy, but excess activation is associated with preeclampsia. Terminal complement activation generates C5b-9, the lytic membrane attack complex, which mediates organ damage. We hypothesize that activation of C5b-9 is increased in women with hypertensive disorders of pregnancy and adverse outcomes Study Design We assessed urine and plasma C5b-9 levels in hypertensive subjects from project COPA (COmplement and Preeclampsia in the Americas), an IRB approved, multi-center observational study, which enrolled subjects from 6 centers and 3 cities in Colombia (Bogotá, Cartagena and Medellín; Nov 15-Jul 16). Hypertensive subjects enrolled in blocks by gestational age ( ≤ or ≥ 34 weeks) and diagnosis (ACOG criteria): 1. chronic hypertension (CHTN); 2. gestational hypertension (GHTN); 3. preeclampsia (PE) and; 4. PE with severe features (PE-SF). COPA was powered for PE-SF (n=100). Clinical data, urine and plasma were collected by trained coordinators, with C5b-9 measured by enzyme linked immunosorbent assays (Human C5b-9 ELISA, BD Biosciences). Maternal and neonatal outcomes were assessed individually and as composite outcomes. Data were analyzed by Chi-square, t-test and logistic regression Results 293 subjects were evaluated [CHTN (n=42), GHTN (n=92), PE (n=58), PE-SF (n=101)]. Adverse maternal and neonatal outcomes, by plasma C5b-9 quartiles 1-4 (pC5b9, Q1-4), are shown in Table 1. Composite maternal outcomes were increased with low pC5b9 (Q1, ≤1443 ng/ml), particularly for those ≥ 34wks (OR 2.93, 95% CI 1.0-8.6, p=0.05). For neonates, preterm birth (PTB) was increased with lower pC5b9 levels (PTB, 2870 ± 1904 vs. term, 3572 ± 2262 ng/ml, p=0.006). Adverse outcomes, by urine C5b-9 (uC5b9) quartiles, are shown in Table 2. They were more common with high uC5b9 levels (Q4, ≥8.49 ng/ml), predominantly due to increased kidney injury (OR 3.0, 95%CI 1.1-8.4, p=0.036) and PTB (OR 2.0, 95% CI 1.2-3.5, p=0.01) Conclusion We describe a novel pattern of complement activation (low plasma / high urine C5b-9), which associates with adverse maternal and neonatal outcomes in women with hypertensive disorders of pregnancy. We postulate that excess complement activation results in kidney injury and depletion of complement factors in plasma, with resultant pregnancy complications.spa
dc.format.extent2spa
dc.format.mimetypeapplication/pdfspa
dc.language.isoengspa
dc.publisherElsevierspa
dc.type.hasversioninfo:eu-repo/semantics/publishedVersionspa
dc.rightsinfo:eu-repo/semantics/openAccessspa
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/2.5/co/*
dc.titleExcess complement activation is associated with adverse outcomes in women with hypertensive disorders of pregnancyspa
dc.typeinfo:eu-repo/semantics/articlespa
dc.publisher.groupNacer, Salud Sexual y Reproductivaspa
dc.identifier.doi10.1016/j.ajog.2017.10.265-
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85spa
dc.rights.accessrightshttp://purl.org/coar/access_right/c_abf2spa
dc.identifier.eissn1097-6868-
oaire.citationtitleAmerican Journal of Obstetrics and Gynecologyspa
oaire.citationstartpage205spa
oaire.citationendpage206spa
oaire.citationvolume218spa
oaire.citationissue1 Suplementospa
dc.rights.creativecommonshttps://creativecommons.org/licenses/by-nc-nd/4.0/spa
dc.publisher.placeNueva York, Estados Unidosspa
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1spa
dc.type.redcolhttps://purl.org/redcol/resource_type/ARTspa
dc.type.localArtículo de investigaciónspa
dc.subject.decsActivación de Complemento-
dc.subject.decsComplement Activation-
dc.subject.decsPreeclampsia-
dc.subject.decsPre-Eclampsia-
dc.subject.decsComplejo de Ataque a Membrana del Sistema Complemento-
dc.subject.decsComplement Membrane Attack Complex-
dc.description.researchgroupidCOL0061636spa
dc.relation.ispartofjournalabbrevAm. J. Obstet. Gynecol.spa
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