Investigation of thrombin generation assay to predict vaso-occlusive crisis in adulthood with sickle cell disease.

hemoglobinopathy hypercoagulability sickle cell disease thrombin generation assay vaso-occlusive crisis

Journal

Frontiers in cardiovascular medicine
ISSN: 2297-055X
Titre abrégé: Front Cardiovasc Med
Pays: Switzerland
ID NLM: 101653388

Informations de publication

Date de publication:
2022
Historique:
received: 25 02 2022
accepted: 20 09 2022
entrez: 24 10 2022
pubmed: 25 10 2022
medline: 25 10 2022
Statut: epublish

Résumé

Sickle cell disease (SCD) is an inherited hemoglobinopathy disorder. The main consequence is synthesis of hemoglobin S leading to chronic hemolysis associated with morbidity. The aim of this study was to investigate Thrombin Generation Assay (TGA) to assess hypercoagulability in SCD and TGA parameters as biomarkers of vaso-occlusive crisis (VOC) risk and hospitalization within 1 year. We performed TGA in platelet poor plasma (PPP) with 1 pM of tissue factor and 4 μM of phospholipid-standardized concentration, in duplicate for patients and controls. We measured thrombomodulin (TM), soluble endothelial Protein C Receptor and Tissue Factor Pathway Inhibitor (TFPI). A total of 113 adult patients with SCD, 83 at steady state and 30 during VOC, and 25 healthy controls matched on age and gender were included. Among the 83 patients at steady state, (36 S/S-1 S/β We have demonstrated a hypercoagulable state in SCD associated with chronic hemolysis. These preliminary findings suggest that TGA parameters, as ETP and peak, could be used to predict VOC development within 1 year.

Identifiants

pubmed: 36277754
doi: 10.3389/fcvm.2022.883812
pmc: PMC9579298
doi:

Types de publication

Journal Article

Langues

eng

Pagination

883812

Informations de copyright

Copyright © 2022 Feugray, Kasonga, Grall, Dumesnil, Benhamou, Brunel, Le Cam Duchez, Lahary and Billoir.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Guillaume Feugray (G)

Vascular Hemostasis Unit, CHU Rouen, Normandie Université, UNIROUEN, INSERM U1096, Rouen, France.

Fiston Kasonga (F)

Vascular Hemostasis Unit, CHU Rouen, Rouen, France.

Maximilien Grall (M)

Department of Internal Medicine, CHU Rouen, Rouen, France.

Cécile Dumesnil (C)

Department of Pediatric Onco-Hematology, CHU Rouen, Rouen, France.

Ygal Benhamou (Y)

Department of Internal Medicine, CHU Rouen, Normandie Université, UNIROUEN, INSERM U1096, Rouen, France.

Valery Brunel (V)

Department of General Biochemistry, CHU Rouen, Rouen, France.

Véronique Le Cam Duchez (V)

Vascular Hemostasis Unit, CHU Rouen, Normandie Université, UNIROUEN, INSERM U1096, Rouen, France.

Agnès Lahary (A)

Hematology Laboratory, CHU Rouen, Rouen, France.

Paul Billoir (P)

Vascular Hemostasis Unit, CHU Rouen, Normandie Université, UNIROUEN, INSERM U1096, Rouen, France.

Classifications MeSH