Effect of DDAVP on Platelet Activation and Platelet-Derived Microparticle Generation.


Journal

Hamostaseologie
ISSN: 2567-5761
Titre abrégé: Hamostaseologie
Pays: Germany
ID NLM: 8204531

Informations de publication

Date de publication:
Jun 2022
Historique:
pubmed: 18 6 2021
medline: 6 7 2022
entrez: 17 6 2021
Statut: ppublish

Résumé

 The way by which 1-deamino-8-D-arginine vasopressin (DDAVP) acts on platelets remains unclear. Data from the literature tend to show that there is no definite effect on platelet activation, but recent work has suggested that a subtype of platelets, activated by the combined action of collagen and thrombin, was triggered by DDAVP. Moreover, platelet microparticles (PMPs), which have been shown to be procoagulant, have rarely been studied in this context. The goal of this study was to analyze the effects of DDAVP on PMPs' release through platelet activation.  Fifteen out of 18 consecutive patients undergoing a therapeutic test with DDAVP were included. They were suffering from factor VIII deficiency or from von Willebrand disease. The expression of P-selectin and PAC-1 binding on platelets and the numbers of circulating PMPs were evaluated ex vivo before and after DDAVP infusion. Peripheral blood was collected on CTAD to limit artifactual platelet activation.  DDAVP induced a significant decrease of platelet counts and volume. Only small changes of P-selectin expression and PAC-1 binding were observed. Considering PMPs, two populations of patients could be defined, respectively, with (120%,  This study shows that DDAVP induces the generation/release of PMPs in some patients with factor VIII deficiency and von Willebrand disease 1 hour after DDAVP infusion.

Sections du résumé

BACKGROUND BACKGROUND
 The way by which 1-deamino-8-D-arginine vasopressin (DDAVP) acts on platelets remains unclear. Data from the literature tend to show that there is no definite effect on platelet activation, but recent work has suggested that a subtype of platelets, activated by the combined action of collagen and thrombin, was triggered by DDAVP. Moreover, platelet microparticles (PMPs), which have been shown to be procoagulant, have rarely been studied in this context. The goal of this study was to analyze the effects of DDAVP on PMPs' release through platelet activation.
METHODS METHODS
 Fifteen out of 18 consecutive patients undergoing a therapeutic test with DDAVP were included. They were suffering from factor VIII deficiency or from von Willebrand disease. The expression of P-selectin and PAC-1 binding on platelets and the numbers of circulating PMPs were evaluated ex vivo before and after DDAVP infusion. Peripheral blood was collected on CTAD to limit artifactual platelet activation.
RESULTS RESULTS
 DDAVP induced a significant decrease of platelet counts and volume. Only small changes of P-selectin expression and PAC-1 binding were observed. Considering PMPs, two populations of patients could be defined, respectively, with (120%,
CONCLUSION CONCLUSIONS
 This study shows that DDAVP induces the generation/release of PMPs in some patients with factor VIII deficiency and von Willebrand disease 1 hour after DDAVP infusion.

Identifiants

pubmed: 34139772
doi: 10.1055/a-1476-7768
doi:

Substances chimiques

P-Selectin 0
von Willebrand Factor 0
Arginine Vasopressin 113-79-1
Deamino Arginine Vasopressin ENR1LLB0FP

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

185-192

Commentaires et corrections

Type : ErratumIn

Informations de copyright

Thieme. All rights reserved.

Déclaration de conflit d'intérêts

The authors declare that they have no conflict of interest.

Auteurs

Matthieu Persyn (M)

Service d'Hématologie Biologique, CHU de Nantes, Nantes, France.

Nicolas Athanase (N)

Service d'Hématologie Biologique, CHU de Nantes, Nantes, France.

Marc Trossaërt (M)

Service d'Hématologie Biologique, CHU de Nantes, Nantes, France.
Centre de Traitement de l'Hémophilie, CHU de Nantes, Nantes, France.

Marianne Sigaud (M)

Service d'Hématologie Biologique, CHU de Nantes, Nantes, France.
Centre de Traitement de l'Hémophilie, CHU de Nantes, Nantes, France.

Catherine Ternisien (C)

Service d'Hématologie Biologique, CHU de Nantes, Nantes, France.
Centre de Traitement de l'Hémophilie, CHU de Nantes, Nantes, France.

Marie C Béné (MC)

Service d'Hématologie Biologique, CHU de Nantes, Nantes, France.

Marc Fouassier (M)

Service d'Hématologie Biologique, CHU de Nantes, Nantes, France.
Centre de Traitement de l'Hémophilie, CHU de Nantes, Nantes, France.

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Classifications MeSH