Venous thrombosis and predictors of relapse in eosinophil-related diseases.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
18 03 2021
Historique:
received: 30 11 2020
accepted: 08 03 2021
entrez: 19 3 2021
pubmed: 20 3 2021
medline: 12 10 2021
Statut: epublish

Résumé

Eosinophils have widespread procoagulant effects. Eosinophilic cardiovascular toxicity mostly consists of endomyocardial damage or eosinophilic vasculitis, while reported cases of venous thrombosis (VT) are scarce. We aimed to report on the clinical features and treatment outcomes of patients with unexplained VT and eosinophilia, and to identify predictors of relapse. This retrospective, multicenter, observational study included patients aged over 15 years with VT, concomitant blood eosinophilia ≥ 1G/L and without any other moderate-to-strong contributing factors for VT. Fifty-four patients were included. VT was the initial manifestation of eosinophil-related disease in 29 (54%) patients and included pulmonary embolism (52%), deep venous thrombosis (37%), hepatic (11%) and portal vein (9%) thromboses. The median [IQR] absolute eosinophil count at VT onset was 3.3G/L [1.6-7.4]. Underlying eosinophil-related diseases included FIP1L1-PDGFRA-associated chronic myeloid neoplasm (n = 4), Eosinophilic Granulomatosis with Polyangiitis (n = 9), lymphocytic (n = 1) and idiopathic (n = 29) variants of hypereosinophilic syndrome. After a median [IQR] follow-up of 24 [10-62] months, 7 (13%) patients had a recurrence of VT. In multivariate analysis, persistent eosinophilia was the sole variable associated with a shorter time to VT relapse (HR 7.48; CI95% [1.94-29.47]; p = 0.015). Long-term normalization of eosinophil count could prevent the recurrence of VT in a subset of patients with unexplained VT and eosinophilia ≥ 1G/L.

Identifiants

pubmed: 33737704
doi: 10.1038/s41598-021-85852-9
pii: 10.1038/s41598-021-85852-9
pmc: PMC7973521
doi:

Substances chimiques

FIP1L1 protein, human 0
mRNA Cleavage and Polyadenylation Factors 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

6388

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Auteurs

Valériane Réau (V)

Department of Internal and Geriatric Medicine, Henri Mondor Hospital, Assistance Publique-Hôpitaux de Paris, Créteil, France.
National Reference Center for Hypereosinophilic Syndromes, CEREO, France.

Alexandre Vallée (A)

Department of Clinical Research and Innovation (DRCI), Hôpital Foch, 92150, Suresnes, France.

Benjamin Terrier (B)

Department of Internal Medicine, National Referral Center for Systemic and Autoimmune Diseases, Cochin Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.

Aurélie Plessier (A)

Department of Hepatology, Beaujon Hospital, Assistance Publique-Hôpitaux de Paris, Clichy, France.

Noémie Abisror (N)

Department of Internal Medicine, Saint Antoine Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.

Félix Ackermann (F)

National Reference Center for Hypereosinophilic Syndromes, CEREO, France.
Department of Internal Medicine, Hôpital Foch, 40, rue Worth, 92151, Suresnes Cedex, France.

Ruben Benainous (R)

Department of Internal Medicine, Avicenne Hospital, Assistance Publique-Hôpitaux de Paris, Bobigny, France.

Gérôme Bohelay (G)

Department of Dermatology, Avicenne Hospital, Assistance Publique-Hôpitaux de Paris, Bobigny, France.

Marie-Laure Chabi-Charvillat (ML)

Department of Radiology, Foch Hospital, Suresnes, France.

Divi Cornec (D)

Department of Rheumatology, Brest University Hospital, Brest, France.

Anne-Claire Desbois (AC)

Department of Internal Medicine, Pitié-Salpêtrière Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.

Stanislas Faguer (S)

Department of Nephrology, Toulouse University Hospital, Toulouse, France.

Nathalie Freymond (N)

Department of Pulmonology, Lyon University Hospital, Lyon, France.

Antoine Gaillet (A)

National Reference Center for Hypereosinophilic Syndromes, CEREO, France.
Department of Internal Medicine, Hôpital Foch, 40, rue Worth, 92151, Suresnes Cedex, France.

Mohamed Hamidou (M)

Department of Internal Medicine, Hôtel-Dieu University Hospital, Nantes, France.

Martin Killian (M)

Department of Internal Medicine, Saint-Etienne University Hospital, Saint-Etienne, France.

Sylvain Le Jeune (S)

Department of Internal Medicine, Avicenne Hospital, Assistance Publique-Hôpitaux de Paris, Bobigny, France.

Anne Marchetti (A)

Department of Dermatology, Lyon-Sud Hospital, Pierre-Bénite, France.

Guy Meyer (G)

Pulmonology and Intensive Care Service, Georges Pompidou European Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.

Francisco Osorio-Perez (F)

Department of Internal Medicine, Dax-Côte D'Argent Hospital, Dax, France.

Kewin Panel (K)

National Reference Center for Hypereosinophilic Syndromes, CEREO, France.
Department of Internal Medicine, Hôpital Foch, 40, rue Worth, 92151, Suresnes Cedex, France.

Pierre-Emmanuel Rautou (PE)

Department of Hepatology, Beaujon Hospital, Assistance Publique-Hôpitaux de Paris, Clichy, France.

Julien Rohmer (J)

National Reference Center for Hypereosinophilic Syndromes, CEREO, France.
Department of Internal Medicine, Hôpital Foch, 40, rue Worth, 92151, Suresnes Cedex, France.

Nicolas Simon (N)

Department of Internal Medicine, Grenoble Alpes University Hospital, Grenoble, France.

Colas Tcherakian (C)

Department of Pulmonology, Foch Hospital, Suresnes, France.

Marc Vasse (M)

Department of Clinical Biology, Foch Hospital, Suresnes, France.
UMR-S INSERM 1176, Université Paris-Saclay, Le Kremlin-Bicêtre, France.

Elina Zuelgaray (E)

Department of Dermatology, Saint Louis, Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.

Guillaume Lefevre (G)

National Reference Center for Hypereosinophilic Syndromes, CEREO, France.
Department of Internal Medicine, Lille University Hospital, Lille, France.

Jean-Emmanuel Kahn (JE)

National Reference Center for Hypereosinophilic Syndromes, CEREO, France.
Department of Internal Medicine, Ambroise Paré Hospital, Assistance Publique-Hôpitaux de Paris, Boulogne-Billancourt, France.

Matthieu Groh (M)

National Reference Center for Hypereosinophilic Syndromes, CEREO, France. m.groh@hopital-foch.com.
Department of Internal Medicine, Hôpital Foch, 40, rue Worth, 92151, Suresnes Cedex, France. m.groh@hopital-foch.com.

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