Platelet features allow to differentiate immune thrombocytopenia from inherited thrombocytopenia.


Journal

Annals of hematology
ISSN: 1432-0584
Titre abrégé: Ann Hematol
Pays: Germany
ID NLM: 9107334

Informations de publication

Date de publication:
Nov 2021
Historique:
received: 13 05 2021
accepted: 18 08 2021
pubmed: 15 9 2021
medline: 26 10 2021
entrez: 14 9 2021
Statut: ppublish

Résumé

Immune thrombocytopenia (ITP) is an acquired bleeding disorder, for which no specific diagnostic test exists. Inherited thrombocytopenia (IT) can mimic ITP and lead to unappropriated management with significant morbidity. Here, in small cohorts of these two disorders, we explored whether platelet sialylation and platelet activation could allow to discriminate the two conditions. We also aimed to confirm the value of immature platelet counts in this discrimination. Platelet sialylation and the expression level of P-selectin were assessed by multiparameter flow cytometry. Immature platelets were estimated on a Sysmex XN 9000 analyzer. No significant difference in platelet sialylation was observed between ITP and IT. Contrarily, platelet activation was significantly higher in ITP patients (p = 0.008). The immature platelet fraction, as previously demonstrated, was significantly lower in the ITP group compared to the IT group (p = 0.014). That statistical significance was achieved in this small pilot study suggests that the two easily available assays of immature platelet count and P-selectin expression could help physicians to reach the proper diagnosis in complex cases of thrombocytopenia.

Identifiants

pubmed: 34519886
doi: 10.1007/s00277-021-04651-4
pii: 10.1007/s00277-021-04651-4
doi:

Substances chimiques

P-Selectin 0
SELP protein, human 0
Sialic Acids 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2677-2682

Informations de copyright

© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Références

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Auteurs

Guillaume Bonnard (G)

Service d'Hématologie Biologique, Hôtel Dieu, CHU de Nantes, Nantes, France. gp.bonnard@gmail.com.
Centre de ressources et de compétences-Maladies hémorragiques constitutionnelles, CHU de Nantes, Nantes, France. gp.bonnard@gmail.com.
Service de Médecine Interne, Hôtel Dieu, CHU de Nantes, Nantes, France. gp.bonnard@gmail.com.

Antoine Babuty (A)

Service d'Hématologie Biologique, Hôtel Dieu, CHU de Nantes, Nantes, France.
Centre de ressources et de compétences-Maladies hémorragiques constitutionnelles, CHU de Nantes, Nantes, France.

Romain Collot (R)

Service D'Hématologie Clinique, Hôtel Dieu, CHU de Nantes, Nantes, France.

Domitille Costes (D)

Service D'Hématologie Clinique, Hôtel Dieu, CHU de Nantes, Nantes, France.

Nicolas Drillaud (N)

Service d'Hématologie Biologique, Hôtel Dieu, CHU de Nantes, Nantes, France.
Centre de ressources et de compétences-Maladies hémorragiques constitutionnelles, CHU de Nantes, Nantes, France.

Marion Eveillard (M)

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

Antoine Néel (A)

Service de Médecine Interne, Hôtel Dieu, CHU de Nantes, Nantes, France.

Alexandra Espitia (A)

Service de Médecine Interne, Hôtel Dieu, CHU de Nantes, Nantes, France.

Agathe Masseau (A)

Service de Médecine Interne, Hôtel Dieu, CHU de Nantes, Nantes, France.

Anaïs Wahbi (A)

Service de Médecine Interne, Hôtel Dieu, CHU de Nantes, Nantes, France.

Mohamed Hamidou (M)

Service de Médecine Interne, Hôtel Dieu, CHU de Nantes, Nantes, France.

Marie C Béné (MC)

Service d'Hématologie Biologique, Hôtel Dieu, CHU de Nantes, Nantes, France.
Centre de ressources et de compétences-Maladies hémorragiques constitutionnelles, CHU de Nantes, Nantes, France.

Marc Fouassier (M)

Service d'Hématologie Biologique, Hôtel Dieu, CHU de Nantes, Nantes, France.
Centre de ressources et de compétences-Maladies hémorragiques constitutionnelles, CHU de Nantes, Nantes, France.

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