Evidence map›Paper›PMID 40682262›Full record

ArticleJournal of diabetes science and technology2025

Increased Glycemic Variability in Patients With Chronic Pancreatitis and Diabetes Compared to Type 2 Diabetes.

Line Davidsen, Morten Hasselstrøm Jensen, Thomas Kronborg, Stine Hangaard, Peter Vestergaard, Asbjørn Mohr Drewes, Filip Krag Knop, Simon Lebech Cichosz, Søren Schou Olesen

Abstract read
In one paragraph

Article in Journal of diabetes science and technology, 2025. 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
–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

2 citing papers in PubMed.

  1. Article
  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.

Line DavidsenCentre for Pancreatic Diseases and Mech-Sense, Department of Gastroenterology and Hepatology, Aalborg University Hospital, Aalborg, Denmark.ORCID 0000-0002-1120-8144
Morten Hasselstrøm JensenDepartment of Health Science and Technology, Aalborg University, Aalborg, Denmark.ORCID 0000-0002-6649-8644
Thomas KronborgDepartment of Health Science and Technology, Aalborg University, Aalborg, Denmark.ORCID 0000-0002-2693-0527
Stine HangaardDepartment of Health Science and Technology, Aalborg University, Aalborg, Denmark.ORCID 0000-0003-0395-3563
Peter VestergaardClinical Institute, Aalborg University, Aalborg, Denmark.
Asbjørn Mohr DrewesCentre for Pancreatic Diseases and Mech-Sense, Department of Gastroenterology and Hepatology, Aalborg University Hospital, Aalborg, Denmark.
Filip Krag KnopCenter for Clinical Metabolic Research, Gentofte Hospital, University of Copenhagen, Hellerup, Denmark.
Simon Lebech CichoszDepartment of Health Science and Technology, Aalborg University, Aalborg, Denmark.ORCID 0000-0002-3484-7571
Søren Schou OlesenCentre for Pancreatic Diseases and Mech-Sense, Department of Gastroenterology and Hepatology, Aalborg University Hospital, Aalborg, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGlycemic variability in diabetes secondary to pancreatic diseases (pancreatic diabetes) remains unclear. We compared glycemic control and variability in patients with pancreatic diabetes and a matched group of individuals with type 2 diabetes using continuous glucose monitoring (CGM).

methodsWe included 30 patients with chronic pancreatitis and insulin-treated secondary diabetes and 30 individuals with insulin-treated type 2 diabetes (matched on HbA1c, age, and sex). Participants wore a blinded CGM for 20±2 days. Glycemic variability was assessed using coefficient of variation (CV), standard deviation (SD), mean amplitude of glycemic excursions (MAGE), and continuous overall net glycemic action (CONGA) at 1 and 2-hour intervals. Glycemic control was evaluated based on time spent in predefined glucose ranges: >250 mg/dL, 181 to 250 mg/dL, 70 to 180 mg/dL (target range), 54 to 69 mg/dL, and <54 mg/dL. CGM parameters were compared between groups.

resultsAll CGM-derived measures of glycemic variability (CV, SD, MAGE, CONGA1, and CONGA2) were significantly higher in patients with chronic pancreatitis and diabetes compared to individuals with type 2 diabetes (

conclusionPatients with pancreatic diabetes have higher glycemic variability than individuals with type 2 diabetes despite comparable levels of HbA1c.

Indexed as

continuous glucose monitoringglycemic variabilityhypoglycemiapancreatic diabetes

Identifiers

PMID40682262
PMCPMC12276207

What Socratic holds

Textmetadata
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 Socratic graph.