Cystic fibrosis.

Bronchiectasis CFTR modulators Cystic fibrosis transmembrane conductance regulator (CFTR) Pseudomonas aeruginosa

Journal

Presse medicale (Paris, France : 1983)
ISSN: 2213-0276
Titre abrégé: Presse Med
Pays: France
ID NLM: 8302490

Informations de publication

Date de publication:
27 Jul 2023
Historique:
received: 31 05 2023
accepted: 19 07 2023
pubmed: 30 7 2023
medline: 30 7 2023
entrez: 29 7 2023
Statut: aheadofprint

Résumé

Cystic fibrosis (CF) is an autosomal recessive genetic disease caused by variants in the gene encoding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. CFTR dysfunction results in abnormal chloride and bicarbonate transport in epithelial cells, leading to a multiorgan disease dominated by respiratory and digestive manifestations. The respiratory disease, which is characterized by airway mucus plugging, chronic bacterial infection and progressive development of bronchiectasis, may lead to chronic respiratory failure, which is the main cause of premature death in people with CF. Over the past 50 years, major progress has been obtained by implementing multidisciplinary care, including nutritional support, airway clearance techniques and antibiotics in specialized CF centers. The past 10 years have further seen the progressive development of oral medications, called CFTR modulators, that partially restore ion transport and lead to a major improvement in clinical manifestations and lung function, presumably resulting in longer survival. Although an increasing proportion of people with CF are being treated with CFTR modulators, challenges remain regarding access to CFTR modulators due to their high cost, and their lack of marketing approval and/or effectiveness in people with rare CFTR variants. The anticipated increase in the number of adults with CF and their aging also challenge the current organization of CF care. The purpose of this review article is to describe current status and future perspective of CF disease and care.

Identifiants

pubmed: 37516246
pii: S0755-4982(23)00006-4
doi: 10.1016/j.lpm.2023.104169
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

104169

Informations de copyright

Copyright © 2023 Elsevier Masson SAS. All rights reserved.

Déclaration de conflit d'intérêts

Disclosure of interest IF. Clinical trials: acting as main investigator, coordinator or main experimenter for Abbvie, Bayer, Boehringer Ingelheim, GSK, Insmed, Vertex Pharmaceuticals, Zambon; One-off interventions: advisory activity for AbbVie, Boehringer Ingelheim, Kither Biotech, Vertex Pharmaceuticals; Substantial financial contributions to the budget of an institution you are responsible for European Cystic Fibrosis Society. PRB. Clinical trials: acting as main investigator, coordinator or main experimenter for Insmed; One-off interventions: advisory activity for Astra-Zeneca, Chiesi, GSK, Insmed, MSD, Viatris, Vertex, Zambon; Substantial financial contributions to the budget of an institution you are responsible for GSK, Vertex, Association Vaincre la Mucoviscidose, Société Française de la Mucoviscidose, Filière MUCO-CFTR.

Auteurs

Isabelle Fajac (I)

Department of Respiratory Medicine and National Cystic Fibrosis Reference Centre, Cochin Hospital, Assistance Publique Hôpitaux de Paris, 27 rue du faubourg Saint-Jacques, 75014 Paris, France; Université Paris Cité, Inserm U1016, Institut Cochin, 24 rue du faubourg Saint-Jacques, 75014 Paris, France; ERN-LUNG, CF Core Network, Frankfurt, Germany. Electronic address: isabelle.fajac@aphp.fr.

Pierre-Régis Burgel (PR)

Department of Respiratory Medicine and National Cystic Fibrosis Reference Centre, Cochin Hospital, Assistance Publique Hôpitaux de Paris, 27 rue du faubourg Saint-Jacques, 75014 Paris, France; Université Paris Cité, Inserm U1016, Institut Cochin, 24 rue du faubourg Saint-Jacques, 75014 Paris, France; ERN-LUNG, CF Core Network, Frankfurt, Germany. Electronic address: pierre-regis.burgel@aphp.fr.

Classifications MeSH