Thromb Haemost 1997; 77(06): 1096-1103
DOI: 10.1055/s-0038-1656119
Clinical Studies
Schattauer GmbH Stuttgart

Prospective Evaluation of the Prevalence of Haemostasis Abnormalities in Unexplained Primary Early Recurrent Miscarriages

The Nímes Obstetricians and Haematologists (NOHA) Study
Jean-Christophe Gris
1   The Consultations et Laboratoire d’Hématologie, CHU, Nimes
2   Laboratoire d’Hématologie, Faculté de Pharmacie, Montpellier
,
Sylvie Ripart-Neveu
3   Service de Gynécologie-Obstétrique, CHU NTmes
,
Claude Maugard
1   The Consultations et Laboratoire d’Hématologie, CHU, Nimes
,
Marie-Laure Tailland
3   Service de Gynécologie-Obstétrique, CHU NTmes
,
Sophie Brun
1   The Consultations et Laboratoire d’Hématologie, CHU, Nimes
,
Christophe Courtieu
3   Service de Gynécologie-Obstétrique, CHU NTmes
,
Christine Biron
4   Laboratoire d’Hématologie, CHU, Montpellier
,
Méderic Hoffet
3   Service de Gynécologie-Obstétrique, CHU NTmes
,
Bernard Hédon
5   Service de Gynécologie-Obstétrique, CHU, Montpellier, France
,
Pierre Marés
2   Laboratoire d’Hématologie, Faculté de Pharmacie, Montpellier
› Author Affiliations
Further Information

Publication History

Received 09 August 1996

Accepted after revision 06 March 1997

Publication Date:
12 July 2018 (online)

Summary

The prevalence of haemostasis abnormalities was evaluated in 500 consecutive women with unexplained primary recurrent miscarriages. Two matched reference groups with no antecedent of miscarriage were studied: 100 healthy mothers and 50 childless women.

In the prospective part of the study, we found 9.4% of the patients (95% C.I.: 6.8-12%) with an isolated factor XII deficiency, 7.4% of the patients (5.0-9.8%) with primary antiphopholipid antibodies, 47% of the patients (42.6-51.4%) with an insufficient response to the venous occlusion test and an isolated hypofibri- nolysis was found in 42.6% (38.2-47%) of the patients (reference groups: respectively 0/150, 3/150, 2/150, 2/150, pclO’3). Willebrand disease, fibrinogen deficiency, antithrombin, protein C or protein S deficiencies were not more frequent in recurrent aborters than in members of the reference groups. In the retrospective part of the study, cases of plasma resistance to activated protein C were not abnormally frequent.

Patients had higher Willebrand factor antigen (vWF), tissue-type plasminogen activator antigen (t-PA), plasminogen activator inhibitor activity (PAI) and D-dimers (D-Di) than the reference women. Values of vWF, t-PA, PAI and D-Di were altogether correlated but were not related to C-reactive protein concentrations. Among patients, those with an antiphospholipid syndrome and those with an insufficient response to the venous occlusion test had higher vWF, t-PA, PAI and D-Di values than the patients with none of the haemostasis-related abnormalities.

Thus, factor XII deficiency and hypofibrinolysis (mainly high PAI) are the most frequent haemostasis-related abnormalities found in unexplained primary recurrent aborters. In patients with antiphospholipid antibodies or hypofibrinolysis, there is a non-inflammatory ongoing chronic elevation of markers of endothelial stimulation associated with coagulation activation. This should allow to define subgroups of patients for future therapeutic trials.

 
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