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Obstetric antiphospholipid syndrome: early variations of angiogenic factors are associated with adverse outcomes

Authors :
Erick Mercier
Antonia Perez-Martin
Sylvie Bouvier
Ève Mousty
Isabelle Quéré
Eva Cochery-Nouvellon
Vincent Letouzey
Jean-Pierre Balducchi
Jean-Christophe Gris
Centre Hospitalier Universitaire de Nîmes (CHU Nîmes)
Caractéristiques féminines des dysfonctions des interfaces cardio-vasculaires (EA 2992)
Université Montpellier 1 (UM1)-Université de Montpellier (UM)
Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier)
Institut des Biomolécules Max Mousseron [Pôle Chimie Balard] (IBMM)
Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université de Montpellier (UM)-Ecole Nationale Supérieure de Chimie de Montpellier (ENSCM)
Source :
Haematologica, Haematologica, Ferrata Storti Foundation, 2017, 102 (5), pp.835-842. ⟨10.3324/haematol.2016.155184⟩
Publication Year :
2017
Publisher :
HAL CCSD, 2017.

Abstract

International audience; The prognostic value of angiogenic factors in newly pregnant women with obstetric antiphospholipid syndrome (oAPS) has not been documented. We observed 513 oAPS who experienced three consecutive spontaneous abortions before the 10th week of gestation or one fetal loss at or beyond the 10th week. We assessed the plasma concentrations of the proangiogenic factor placenta growth factor (PIGF) and of the antiangiogenic factor soluble fms-like tyrosine kinase-1 on the eve and on the 4th day of the low-molecular weight heparin-low-dose aspirin treatment. Placenta growth factor and fms-like tyrosine kinase-1 plasma concentrations showed marked increases. Treatment-associated variations of PIGF and of soluble fms-like tyrosine kinase-1 were antagonist risk factors for placenta-mediated complications (PMC) and for severe PMC, for fetal death, stillbirth and neonatal death. The ratio between PIGF increase and soluble fms-like tyrosine kinase-1 was a summary variable whose best cut-off values (1.944.10-2) had high negative predictive values for PMC (0.918) and may be used to help rule out the development of PMC in evolutive pregnancies after 19 completed weeks. The early variations of PIGF and soluble fms-like tyrosine kinase-1 concentrations in newly pregnant oAPS may help to detect patients at low risk of PMC. (clinicaltrials.gov identifier: 02855047).

Details

Language :
English
ISSN :
03906078 and 15928721
Database :
OpenAIRE
Journal :
Haematologica, Haematologica, Ferrata Storti Foundation, 2017, 102 (5), pp.835-842. ⟨10.3324/haematol.2016.155184⟩
Accession number :
edsair.doi.dedup.....5380dbb4dcbef0b79ef665b242db2550