Experience and expectations of pharmacogenetic tests in France.

Genome sequencing Genomic medicine Pharmacogenetics

Journal

Therapie
ISSN: 1958-5578
Titre abrégé: Therapie
Pays: France
ID NLM: 0420544

Informations de publication

Date de publication:
17 Jul 2023
Historique:
received: 24 02 2023
revised: 06 07 2023
accepted: 13 07 2023
medline: 30 7 2023
pubmed: 30 7 2023
entrez: 29 7 2023
Statut: aheadofprint

Résumé

Although French genomic medicine is reaching a turning point in its history and the implementation of genome sequencing in routine is being implemented as part of the France Genomic Medicine 2025 Plan (FGMP), many questions about secondary data management remain to be addressed. In particular, the use of pharmacogenetic (PGx) information that can be extracted from genome data is a concern. We sought to analyze the opinion of French health professionals on their desire to have access to this information. For this purpose, we created a 22-item questionnaire on the experiences, attitudes, expectations, and knowledge of French physicians and pharmacists about PGx. We collected the responses in different groups and determined a knowledge score with the last 3 questions of the questionnaire. Then, we built a prediction model for this score and determined which factors may influence it. Half of the responders were physicians (158/311) and the other half were pharmacists (153/311), and the majority of them worked in a hospital (265/311). Almost two third (62.7%, 195/311) of the responders thought that pharmacogenetic data should be communicated with genomic results for the primary indication within the framework of FGMP, and 89.1% (277/311) of them that PGx tests could be an interesting tool to optimize patients' drug therapy in the future. Only 11.2% (35/311) of the responders reached the maximum knowledge score, while 25.4% (76/311) had already prescribed or recommended a PGx test. This study identified a need for training for French physicians and pharmacists in PGx, particularly given the interest of health professionals in it.

Identifiants

pubmed: 37516659
pii: S0040-5957(23)00103-8
doi: 10.1016/j.therap.2023.07.002
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2023. Published by Elsevier Masson SAS.

Auteurs

Simon Verdez (S)

UMR1231 GAD team, Genetics of Developmental Disorders, Inserm - université Bourgogne-Franche Comté, 21000 Dijon, France; Unité fonctionnelle innovation en diagnostic génomique des maladies rares, FHU-TRANSLAD, CHU de Dijon Bourgogne, 21000 Dijon, France. Electronic address: simon.verdez@chu-dijon.fr.

Marc Bardou (M)

Centre d'investigation clinique, module épidémiologie clinique/essais cliniques, CHU de Dijon, 21000 Dijon, France; Inserm CIC1432, 21000 Dijon, France.

Yannis Duffourd (Y)

UMR1231 GAD team, Genetics of Developmental Disorders, Inserm - université Bourgogne-Franche Comté, 21000 Dijon, France; Unité fonctionnelle innovation en diagnostic génomique des maladies rares, FHU-TRANSLAD, CHU de Dijon Bourgogne, 21000 Dijon, France.

Maxime Luu (M)

Inserm CIC1432, 21000 Dijon, France; Centre d'investigation clinique, module plurithématique, CHU de Dijon, 21000 Dijon, France.

Christel Thauvin-Robinet (C)

UMR1231 GAD team, Genetics of Developmental Disorders, Inserm - université Bourgogne-Franche Comté, 21000 Dijon, France; Unité fonctionnelle innovation en diagnostic génomique des maladies rares, FHU-TRANSLAD, CHU de Dijon Bourgogne, 21000 Dijon, France; Centre de référence maladies rares « déficiences intellectuelles de causes rares », centre de génétique, FHU-TRANSLAD, CHU de Dijon Bourgogne, 21000 Dijon, France; Centre de référence maladies rares « anomalies du développement et syndromes malformatifs », centre de génétique, FHU-TRANSLAD, CHU de Dijon Bourgogne, 21000 Dijon, France.

Laurence Faivre (L)

UMR1231 GAD team, Genetics of Developmental Disorders, Inserm - université Bourgogne-Franche Comté, 21000 Dijon, France; Unité fonctionnelle innovation en diagnostic génomique des maladies rares, FHU-TRANSLAD, CHU de Dijon Bourgogne, 21000 Dijon, France; Centre de référence maladies rares « déficiences intellectuelles de causes rares », centre de génétique, FHU-TRANSLAD, CHU de Dijon Bourgogne, 21000 Dijon, France; Centre de référence maladies rares « anomalies du développement et syndromes malformatifs », centre de génétique, FHU-TRANSLAD, CHU de Dijon Bourgogne, 21000 Dijon, France.

Nicolas Picard (N)

Service de pharmacologie et toxicologie, université de Limoges, Inserm U1248, CHU de Limoges, 87042 Limoges, France.

Classifications MeSH