Evidence map›Paper›PMID 30894563›Full record

ArticleScientific reports2019

Glucose tolerance in Canadian and French cystic fibrosis adult patients.

Quitterie Reynaud, Valérie Boudreau, Sandrine Touzet, Katherine Desjardins, Stéphanie Poupon Bourdy, Emilie Blond, Yves Berthiaume, Rémi Rabasa-Lhoret, Isabelle Durieu

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.6field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 12 citations in OpenAlex.

  1. 20 years of the Montreal Cystic Fibrosis Related Diabetes Screening Cohort: key insights.European respiratory review : an official journal of the European Respiratory Society · 2025
    Review
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 2 countries.

Quitterie ReynaudCentre de référence Adulte de la Mucoviscidose, Service de médecine interne, Hospices civils de Lyon, F-69495, Pierre Bénite, France. quitterie.reynaud@chu-lyon.fr.ORCID 0000-0002-7055-053X
Valérie BoudreauMontreal Clinical Research Institute, Québec, Canada.
Sandrine TouzetHospices Civils de Lyon, Pôle de Santé Publique, Lyon, F-69003, France.
Katherine DesjardinsMontreal Clinical Research Institute, Québec, Canada.
Stéphanie Poupon BourdyHospices Civils de Lyon, Pôle de Santé Publique, Lyon, F-69003, France.
Emilie BlondService de Biochimie et Biologie Moléculaire, Hospices Civils de Lyon, F-69495, Pierre Bénite, France.
Yves BerthiaumeMontreal Clinical Research Institute, Québec, Canada.
Rémi Rabasa-LhoretMontreal Clinical Research Institute, Québec, Canada.
Isabelle DurieuCentre de référence Adulte de la Mucoviscidose, Service de médecine interne, Hospices civils de Lyon, F-69495, Pierre Bénite, France.
Université Claude Bernard Lyon 1 · FRCentre Hospitalier de l’Université de Montréal · CAMontreal Clinical Research Institute · CA

Funding

CIHR
6 · The paper itself

Abstract

Cystic fibrosis (CF)-related diabetes is associated with increased mortality. We analysed the clinical and glycemic profiles of two cohorts of patients treated according to the same guidelines in France and Canada. To investigate incidence differences in phenotypic and glucose abnormalities and to explore the evolution over a 4-year follow-up period, two cohorts of 224 Canadian and 147 French adult CF patients (≥18 years) without treated CF-related diabetes (CFRD) were followed over a 4 year period. In each of these groups, we investigated the longitudinal relationship between glucose tolerance and pulmonary function. An annual 2-hour oral glucose tolerance test was performed: fasting blood glucose (G0) and 2-h blood glucose (G2) were measured. Patients were classified at inclusion according to their glucose tolerance status: Normal glucose tolerant, abnormal glucose tolerant or de novo CFRD. Age, sex ratio and proportion of F508del homozygous patients were not statistically different between both cohorts. Canadian patients had better pulmonary function (median %FEV1 (IQR): 71.0 (55.0-82.0) vs. 64.0 (40.0-78.0), p < 0.001) and greater body mass index (BMI; median BMI in kg/m

Indexed as

AdultBlood GlucoseBody Mass IndexCanadaCystic FibrosisDiabetes MellitusFemaleForced Expiratory Flow RatesFranceGlucose IntoleranceGlucose Tolerance TestHumansInsulinMaleYoung AdultBlood GlucoseInsulin

Identifiers

PMID30894563
PMCPMC6427035
OpenAlexW2924899502

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.