Evidence map›Paper›PMID 29329721›Full record

ArticleJournal of cystic fibrosis : official journal of the European Cystic Fibrosis Society2018

Quantifying fluctuation in glucose levels to identify early changes in glucose homeostasis in cystic fibrosis.

Rossa Brugha, Marie Wright, Suzie Nolan, Nicola Bridges, Siobhán B Carr

Registry-linked trialOpen access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04275479 (Endocrine Diabetes Screening in Patients With Shwachman-Diamond Syndrome DIABETES/ ENDOCRINE SURVEILLANCE IN SDS), which is not on this map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 22% 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.

NCT04275479 terminatednot on this mapstarted 2020, after this paper: background citation

Endocrine Diabetes Screening in Patients With Shwachman-Diamond Syndrome DIABETES/ ENDOCRINE SURVEILLANCE IN SDS

TypeobservationalSponsorWashington University School of MedicineRan2020 to 2022Enrolled11ConditionsShwachman-Diamond SyndromeArmsOral Glucose Tolerance Test, Modified Oral Glucose Tolerance Test, Modified Mixed Meal Tolerance Test, Continuous Glucose Monitor, Food Diary
3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Demographic factors associated with within-individual variability of lung function for adults with cystic fibrosis: A UK registry study.Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society · 2024
    Article
  5. Review
  6. Observational
  7. Observational
  8. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Rossa BrughaPaediatric Respiratory Medicine, Royal Brompton Hospital, London, UK; National Heart and Lung Institute, Imperial College London, London, UK. Electronic address: r.brugha@imperial.ac.uk.
Marie WrightPaediatric Respiratory Medicine, Royal Brompton Hospital, London, UK.
Suzie NolanPaediatric Dietetics, Royal Brompton Hospital, London, UK.
Nicola BridgesPaediatric Endocrinology, Chelsea and Westminster Hospital, London, UK.
Siobhán B CarrPaediatric Respiratory Medicine, Royal Brompton Hospital, London, UK.
Royal Brompton Hospital · GBChelsea and Westminster Hospital · GB

Funding

Department of Health
6 · The paper itself

Abstract

backgroundCystic fibrosis related diabetes (CFRD) is associated with increased morbidity in CF. Variability in physiological systems is associated with dysfunctional homeostasis. We examined whether fluctuation in glucose is a marker of CFRD or "pre-diabetes".

methodsUsing a machine learning approach, we compared glucose IQR to current diagnostic criteria in a review of continuous glucose monitoring data.

resultsAnalysis was performed on 248 studies from 142 children. Calculated IQR (cIQR) was increased between children with CFRD, normal glucose homeostasis and indeterminate status (p<0.0001) and impaired glucose tolerance (p<0.05, Kruskal-Wallis test). In subjects who developed CFRD (n=20), cIQR increased between baseline and diagnosis (1.4mmol/L versus 2.4mmol/L, p<0.0001, Wilcoxon test). Area under the curve for CFRD on the basis of cIQR was 0.865 (p<0.0001). Neither episodes of hypoglycaemia nor cIQR at baseline predicted CFRD.

conclusionsGlucose fluctuation on CGMS can be quantified by calculating the IQR. This information may improve early recognition of abnormal glucose homeostasis.

Indexed as

Blood GlucoseCystic FibrosisDiabetes MellitusPrediabetic StateAdolescentChildEarly DiagnosisFemaleHumansMaleMonitoring, PhysiologicPediatricsUnited KingdomBlood GlucoseContinuous glucose monitoringCystic fibrosisCystic fibrosis related diabetes

Identifiers

PMID29329721
OpenAlexW2784006074

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.