Evidence map›Paper›PMID 38668761›Full record

Trial reportDiabetologia2024

Discordance between mean glucose and time in range in relation to HbA

Sofia Sterner Isaksson, Henrik Imberg, Irl B Hirsch, Erik Schwarcz, Jarl Hellman, Magnus Wijkman, Jan Bolinder, Thomas Nyström, Helene Holmer, Sara Hallström and 4 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Diabetologia, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Observational
  6. Article
  7. Article
  8. Managing discordance between HbADiabetic medicine : a journal of the British Diabetic Association · 2025
    Review
  9. Article
  10. Article
  11. 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

14 authors.

Sofia Sterner IsakssonDepartment of Molecular and Clinical Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.ORCID http://orcid.org/0000-0002-1302-3629
Henrik ImbergDepartment of Molecular and Clinical Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.ORCID http://orcid.org/0000-0001-9447-663X
Irl B HirschUniversity of Washington, School of Medicine, Seattle, WA, USA.ORCID http://orcid.org/0000-0003-1675-8417
Erik SchwarczDepartment of Internal Medicine, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.ORCID http://orcid.org/0000-0003-1961-3192
Jarl HellmanDepartment of Medical Sciences, Uppsala University, Uppsala, Sweden.ORCID http://orcid.org/0000-0001-6187-5511
Magnus WijkmanDepartment of Internal Medicine and Department of Health, Medicine and Caring Sciences, Linköping University, Norrköping, Sweden.ORCID http://orcid.org/0000-0002-4757-9051
Jan BolinderDepartment of Medicine, Karolinska University Hospital Huddinge, Karolinska Institute, Stockholm, Sweden.ORCID http://orcid.org/0000-0003-0035-0142
Thomas NyströmDepartment of Clinical Science and Education, Karolinska Institutet, Södersjukhuset, Stockholm, Sweden.ORCID http://orcid.org/0000-0002-3462-7990
Helene HolmerDepartment of Medicine, Centralsjukhuset, Kristianstad, Sweden.ORCID http://orcid.org/0000-0003-0464-6485
Sara HallströmDepartment of Molecular and Clinical Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.ORCID http://orcid.org/0000-0002-1119-5267
Arndís F ÓlafsdóttirDepartment of Molecular and Clinical Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.ORCID http://orcid.org/0000-0002-2083-2512
Sofia PekkariDepartment of Molecular and Clinical Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.ORCID http://orcid.org/0000-0003-3877-6974
William PolonskyBehavioral Diabetes Institute, San Diego, CA, USA.
Marcus LindDepartment of Molecular and Clinical Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden. marcus.lind@gu.se.ORCID http://orcid.org/0000-0002-3796-9283

Funding

The Swedish State under the agreement between the Swedish government and the county councils, the ALF-agreement ALFGBG-966173
6 · The paper itself

Abstract

aims/hypothesisPrevious studies have shown that individuals with similar mean glucose levels (MG) or percentage of time in range (TIR) may have different HbA

methodsData from the randomised clinical GOLD trial (n=144) and the follow-up SILVER trial (n=98) of adults with type 1 diabetes followed for 2.5 years were analysed. A total of 596 paired HbA

resultsIn the GOLD trial, the mean age of the participants (± SD) was 44±13 years, 63 (44%) were female, and the mean HbA CONCLUSIONS/

interpretationInter-individual variations exist between MG and HbA

Indexed as

Blood GlucoseDiabetes Mellitus, Type 1Glycated HemoglobinAdultBlood Glucose Self-MonitoringFemaleHumansHypoglycemic AgentsMaleMiddle AgedBlood GlucoseGlycated Hemoglobinhemoglobin A1c protein, humanHypoglycemic AgentsContinuous glucose monitoringHbA1cMean glucoseTime in rangeType 1 diabetes

Identifiers

PMID38668761
PMCPMC11343832

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.