Impact of 1h oral glucose tolerance test on the clinical status of adult cystic fibrosis patients over a 4-year period.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2021
Historique:
received: 28 08 2020
accepted: 27 01 2021
entrez: 18 3 2021
pubmed: 19 3 2021
medline: 27 8 2021
Statut: epublish

Résumé

To report the clinical profile associated with G60 and I60 over a 4-year prospective observational period in 2 large cohorts of adult patients with CF. 319 patients were included (210 Canadian and 119 French) and classified according to their inclusion G60 (≥ or < 11.1 mmol/L) and the median inclusion I60 (≥ or < 24 mU/I). Forced expiratory volume in 1 second (FEV1), body mass index (BMI) were collected on OGTT days. Linear mixed regression models were used to assess the effect of G60 and I60. High G60 was not associated to a lower FEV1 at inclusion and the follow-up decline was not higher in the high G60 group (Coefficient [95% CI]: -3.4 [-7.4;0.6], p = 0.0995.). There was no significant association between BMI and G60. Patients with high I60 tended to have a higher mean BMI (+0.5 kg/m2 [0.0 to 1.1], p = 0.05) but no interaction over time was observed. High G60 is not associated with a lower lung function at inclusion nor its decline over a 4-year follow-up. High I60 is slightly associated to a higher weight at inclusion, but not with BMI evolution over time in adult patients.

Identifiants

pubmed: 33735186
doi: 10.1371/journal.pone.0246897
pii: PONE-D-20-26936
pmc: PMC7971459
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0246897

Subventions

Organisme : CIHR
Pays : Canada

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Valérie Boudreau (V)

Montreal Clinical Research Institute, Québec, Canada.
Département de nutrition et de Médecine, Université de Montréal, Montréal, Québec, Canada.

Quitterie Reynaud (Q)

Centre de référence Adulte de la Mucoviscidose, Service de médecine interne, Hospices civils de Lyon, F-69495 Pierre Bénite, France.
Université de Lyon, Équipe d'Accueil Health Services and Performance Research (HESPER) 7425, Lyon, France.

Angélique Denis (A)

Pôle de Santé Publique, Hospices Civils de Lyon, Lyon, France.
Équipe d'Accueil Health Services and Performance Research (HESPER) 7425, Université de Lyon, Lyon, France.

Johann Colomba (J)

Montreal Clinical Research Institute, Québec, Canada.
Département de nutrition et de Médecine, Université de Montréal, Montréal, Québec, Canada.

Sandrine Touzet (S)

Pôle de Santé Publique, Hospices Civils de Lyon, Lyon, France.
Équipe d'Accueil Health Services and Performance Research (HESPER) 7425, Université de Lyon, Lyon, France.

Katherine Desjardins (K)

Montreal Clinical Research Institute, Québec, Canada.

Stéphanie Poupon Bourdy (SP)

Pôle de Santé Publique, Hospices Civils de Lyon, Lyon, France.
Équipe d'Accueil Health Services and Performance Research (HESPER) 7425, Université de Lyon, Lyon, France.

Isabelle Durieu (I)

Centre de référence Adulte de la Mucoviscidose, Service de médecine interne, Hospices civils de Lyon, F-69495 Pierre Bénite, France.
Université de Lyon, Équipe d'Accueil Health Services and Performance Research (HESPER) 7425, Lyon, France.

Rémi Rabasa-Lhoret (R)

Montreal Clinical Research Institute, Québec, Canada.
Département de nutrition et de Médecine, Université de Montréal, Montréal, Québec, Canada.
Cystic fibrosis clinic, Centre Hospitalier de l'Université de Montréal, Montréal, Québec, Canada.

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