Evidence map›Paper›PMID 27048248›Full record

ArticleDiabetologia2016

Changes in beta cell function occur in prediabetes and early disease in the Lepr (db) mouse model of diabetes.

Oanh H Do, Jenny E Gunton, Herbert Y Gaisano, Peter Thorn

Open access · hybridAbstract read
In one paragraph

Article in Diabetologia, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
6.0field-weighted citation impact, top 4% 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

23 citing papers in PubMed, 45 citations in OpenAlex.

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  5. Lessons from a model: early glucagon dysfunction in type 2 diabetes.Pflugers Archiv : European journal of physiology · 2025
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  9. The Emerging Role of Prediabetes and Its Management: Focus on L-Arginine and a Survey in Clinical Practice.High blood pressure & cardiovascular prevention : the official journal of the Italian Society of Hypertension · 2023
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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 2 countries.

Oanh H DoSchool of Biomedical Sciences, University of Queensland, St Lucia, Brisbane, QLD, 4072, Australia.
Jenny E GuntonWestmead Hospital, Sydney, NSW, 2145, Australia.
Herbert Y GaisanoSchool of Medicine, University of Toronto, Toronto, ON, M5S 1A8, Canada.
Peter ThornSchool of Biomedical Sciences, University of Queensland, St Lucia, Brisbane, QLD, 4072, Australia. p.thorn@uq.edu.au.
The University of Queensland · AUThe University of Sydney · AUUniversity of Toronto · CAWestmead Hospital · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aims/hypothesisType 2 diabetes is a progressive disease that increases morbidity and the risk of premature death. Glucose dysregulation, such as elevated fasting blood glucose, is observed prior to diabetes onset. A decline in beta cell insulin secretion contributes to the later stages of diabetes, but it is not known what, if any, functional beta cell changes occur in prediabetes and early disease.

methodsThe Lepr (db) mouse (age 13-18 weeks) was used as a model of type 2 diabetes and a two-photon granule fusion assay was used to characterise the secretory response of pancreatic beta cells.

resultsWe identified a prediabetic state in db/db mice where the animals responded normally to a glucose challenge but have elevated fasting blood glucose. Isolated islets from prediabetic animals secreted more and were bigger. Insulin secretion, normalised to insulin content, was similar to wild type but basal insulin secretion was elevated. There was increased glucose-induced granule fusion with a high prevalence of granule-granule fusion. The glucose-induced calcium response was not changed but there was altered expression of the exocytic machinery. db/db animals at the next stage of disease had overt glucose intolerance. Isolated islets from these animals had reduced insulin secretion, reduced glucose-induced granule fusion events and decreased calcium responses to glucose. CONCLUSIONS/

interpretationBeta cell function is altered in prediabetes and there are further changes in the progression to early disease.

Indexed as

AnimalsDiabetes Mellitus, Type 2Disease Models, AnimalExocytosisFemaleFluorescent Antibody TechniqueInsulinInsulin-Secreting CellsMaleMiceMicroscopy, Electron, ScanningPrediabetic StateReal-Time Polymerase Chain ReactionInsulinBeta cellCompound exocytosisExocytosisInsulin granulesIsletsPrediabetesProgression

Identifiers

PMID27048248
PMCPMC4869737
OpenAlexW2329809781

What Socratic 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 Socratic graph.