Evidence map›Paper›PMID 34917485›Full record

ArticleJournal of clinical & translational endocrinology2022

Cystic fibrosis-related diabetes: Prevalence, screening, and diagnosis.

Swapnil Khare, Marisa Desimone, Nader Kasim, Christine L Chan

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical & translational endocrinology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

25 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Evolving nutrition therapy in cystic fibrosis: Adapting to the CFTR modulator era.Nutrition in clinical practice : official publication of the American Society for Parenteral and Enteral Nutrition · 2025
    Review
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  10. Review
  11. Racial inequities and rareJournal of clinical & translational endocrinology · 2024
    Article
  12. Heliyon · 2024
    Article
  13. Review
  14. Review
  15. Review
  16. Review
  17. Article
  18. Artificial Intelligence Techniques to Predict the Airway Disorders Illness: A Systematic Review.Archives of computational methods in engineering : state of the art reviews · 2023
    Review
  19. Article
  20. 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

4 authors at 4 institutions in 1 country.

Swapnil KhareDivision of Endocrinology, Diabetes and Metabolism, Indiana University-Purdue University, Indianapolis, IN, United States.
Marisa DesimoneDivision of Endocrinology, Diabetes and Metabolism SUNY, Upstate Medical University, Syracuse, NY, United States.
Nader KasimDivision of Pediatric Endocrinology, Michigan State University, Helen Devos Children's Hospital/Spectrum Health, Grand Rapids, MI, United States.
Christine L ChanDepartment of Pediatrics, Division of Pediatric Endocrinology, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Helen DeVos Children's Hospital · USIndiana University – Purdue University Indianapolis · USSUNY Upstate Medical University · USUniversity of Colorado Anschutz Medical Campus · US

Funding

University of Colorado Anschutz Medical Campus DRCP30DK116073 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI LORI SUSSEL · 2020 to 2026
$10.8M
NIDDK NIH HHS P30 DK116073
6 · The paper itself

Abstract

Cystic fibrosis-related diabetes (CFRD) is the most common comorbidity in patients with cystic fibrosis (CF). Prevalence of CFRD increases with age and is greater with severe mutations. Other risk factors associated with CFRD are female sex, pancreatic insufficiency, liver disease, need for gastrostomy tube feedings, history of bronchopulmonary aspergillosis, and poor pulmonary function. CFRD is related to worse clinical outcomes and increased mortality. Early diagnosis and treatment have been shown to improve clinical outcomes. Screening for CFRD is recommended with an annual oral glucose tolerance test (OGTT) starting at age 10 years. Diagnosis of CFRD is made by standard American Diabetes Association (ADA) criteria during baseline health. CFRD can also be diagnosed in individuals with CF during acute illness, while on enteral feeds, and after transplant. In this review we will discuss the epidemiology of CFRD and provide an overview of the advantages and pitfalls of current screening and diagnostic tests for CFRD.

Indexed as

1hG, 1 h glucose2hG, 2 h glucoseA1c, Hemoglobin A1cCF, Cystic FibrosisCFRD, Cystic Fibrosis Related DiabetesContinuous glucose monitoringCystic fibrosis-related diabetesFPG, Fasting Plasma GlucoseHemoglobin A1cOGTT, Oral glucose tolerance testingOral glucose tolerance testPrevalenceScreeningT1DM, Type 1 diabetes mellitusT2DM, Type 2 diabetes mellitus

Identifiers

PMID34917485
PMCPMC8669384
OpenAlexW4200328378

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.