Evidence map›Paper›PMID 40123275›Full record

ArticleHaemophilia : the official journal of the World Federation of Hemophilia2025

Clinical, Phenotypic and Genotypic Characteristics of Von Willebrand Disease in Afro-Caribbeans: Results From a Study in Martinique Island, French West Indies.

Marie-Daniéla Dubois, Olivier Nicolas Pierre-Louis, Serge Pierre-Louis, Pierre Boisseau, Cécile V Denis, Annabelle Dupont, Jenny Goudemand, Caterina Casari, Emmanuelle Jeanpierre, Christophe Zawadzki and 12 more

Abstract read
In one paragraph

Article in Haemophilia : the official journal of the World Federation of Hemophilia, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

22 authors.

Marie-Daniéla DuboisUR5_3 Pathologie Cardiaque, toxicité Environnementale et Envenimations (PC2E), CHU de Martinique (University Hospital of Martinique), Fort de France, France.
Olivier Nicolas Pierre-LouisUR5_3 Pathologie Cardiaque, toxicité Environnementale et Envenimations (PC2E), CHU de Martinique (University Hospital of Martinique), Fort de France, France.
Serge Pierre-LouisCentre de Ressources et de Compétences Maladies Hémorragiques Constitutionnelles, CHU de Martinique, Fort-de-France, France.
Pierre BoisseauService de Génétique Médicale, CHU de Nantes, Nantes, France.
Cécile V DenisLaboratory for Hemostasis, Inflammation & Thrombosis (HITh), Unité Mixte de Recherche 1176, Institut National de la Santé et de la Recherche Médicale, Université Paris-Saclay, Le Kremlin-Bicêtre, France.
Annabelle DupontUniv. Lille, Inserm, CHU Lille, Institut Pasteur de Lille, Lille, France.
Jenny GoudemandService d'hémostase et transfusion, Lille, France.
Caterina CasariLaboratory for Hemostasis, Inflammation & Thrombosis (HITh), Unité Mixte de Recherche 1176, Institut National de la Santé et de la Recherche Médicale, Université Paris-Saclay, Le Kremlin-Bicêtre, France.
Emmanuelle JeanpierreUniv. Lille, Inserm, CHU Lille, Institut Pasteur de Lille, Lille, France.
Christophe ZawadzkiUniv. Lille, Inserm, CHU Lille, Institut Pasteur de Lille, Lille, France.
Béatrice FerreyCentre de Ressources et de Compétences Maladies Hémorragiques Constitutionnelles, CHU de Martinique, Fort-de-France, France.
Johalène RaboutCentre de Ressources et de Compétences Maladies Hémorragiques Constitutionnelles, CHU de Martinique, Fort-de-France, France.
Pascal FuseauService d'Hématologie Biologique, CHU de Martinique, Fort-de-France, France.
Emelyne ChonvilleCentre de Ressources et de Compétences Maladies Hémorragiques Constitutionnelles, CHU de Martinique, Fort-de-France, France.
Franck MichelPharmacie CHU de Martinique, Fort-de-France, France.
Marie-Nadiège YerroCentre de Ressources et de Compétences Maladies Hémorragiques Constitutionnelles, CHU de Martinique, Fort-de-France, France.
Yves GruelLaboratoire d'Hématologie-Hémostase, CHRU de Tours, Hôpital Trousseau, Tours Cedex, France.
Olivier ChristopheLaboratory for Hemostasis, Inflammation & Thrombosis (HITh), Unité Mixte de Recherche 1176, Institut National de la Santé et de la Recherche Médicale, Université Paris-Saclay, Le Kremlin-Bicêtre, France.
Peter J LentingLaboratory for Hemostasis, Inflammation & Thrombosis (HITh), Unité Mixte de Recherche 1176, Institut National de la Santé et de la Recherche Médicale, Université Paris-Saclay, Le Kremlin-Bicêtre, France.ORCID https://orcid.org/0000-0002-7937-3429
Eustase JankyGynaecology, Obstetrics Department, University Hospital of Guadeloupe, Pointe-à-Pitre, France.
Sophie SusenUniv. Lille, Inserm, CHU Lille, Institut Pasteur de Lille, Lille, France.
Rémi NeviereUR5_3 Pathologie Cardiaque, toxicité Environnementale et Envenimations (PC2E), CHU de Martinique (University Hospital of Martinique), Fort de France, France.ORCID https://orcid.org/0000-0002-7966-0110

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSeveral cohort studies have investigated the molecular basis of von Willebrand disease (VWD); very few have focused on the Afro-Caribbean population.

objectivesTo determine the genotypic and phenotypic characterization of VWD in a large cohort of Afro-Caribbean patients living in Martinique. MATERIALS AND

methodsA total of 31 families comprising 63 Afro-Caribbean patients with VWD were enrolled. A standardized questionnaire and blood samples were collected for biological and molecular genetic analyses of von Willebrand factor (VWF). The impact of new missense variants has been predicted by in silico studies.

resultsThe median age of patients was 53 years (range 9-99). The most frequent symptoms were menorrhagia (49%), easy bruising (44%) and prolonged bleeding after tooth extraction (42%). Fifteen patients (24%) had quantitative deficiencies of VWF, of whom 13 (21%) were assigned as VWD-type 1, 1 (1%) as VWD-type 1C and 1 (2%) as VWD-type 3. Forty-five patients were diagnosed with VWD-type 2 (qualitative defects of VWF) (71%). VWD-type 2A was the most frequent, with 36 patients. Seven patients had VWD-type 2M and two patients had VWD-type 2B. Three patients (5%) had an indeterminate effect of the VWF defect due to ISTH BAT at 0. Forty-eight different VWF variants, including 4 novel variants, were identified in 63 patients. The variants consisted of 34 (71%) missense, 7 (15%) synonymous, 3 (6%) frameshifts, 2 (4%) small deletions and 2 (4%) gene conversions.

conclusionsThis study emphasizes the unique distribution of genotypes in our cohort of Afro-Caribbean VWD patients living in Martinique. ESSENTIALS: Genotype-phenotype correlation was assessed in VWD Afro-Caribbean patients with one or more VWF variants. Menorrhagia, easy bruising and prolonged bleeding after tooth extraction are common in VWD patients. Efforts to increase the awareness and diagnosis of VWD have contributed to a better identification of patients with bleeding disorders.

Indexed as

von Willebrand DiseasesAdolescentAdultAgedAged, 80 and overBlack PeopleCaribbean PeopleChildFemaleGenotypeHumansMaleMartiniqueMiddle AgedPhenotypevon Willebrand Factorvon Willebrand FactorbleedingDNA sequencinggenotype‐phenotype relationshipsvariantsvon Willebrand diseasevon Willebrand factor

Identifiers

PMID40123275
PMCPMC12175117

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.