Evidence map›Paper›PMID 41366535›Full record

Trial reportDiabetologia2026

Empagliflozin improves beta cell function independently of relief of glucotoxicity in patients with type 2 diabetes: results from a randomised cross-over study with insulin as comparator.

Roopameera Thirumathyam, Erik A Richter, Gerrit van Hall, Nicoline R Andersen, Per L Madsen, Jens J Holst, Sten Madsbad, Nils B Jørgensen

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Diabetologia, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Roopameera ThirumathyamDepartment of Endocrinology, Hvidovre Hospital, Hvidovre, Denmark.ORCID http://orcid.org/0000-0001-8386-4864
Erik A RichterDepartment of Nutrition, Exercise and Sports, University of Copenhagen, Copenhagen, Denmark.ORCID http://orcid.org/0000-0002-6850-3056
Gerrit van HallDepartment of Clinical Biochemistry, Rigshospitalet, Copenhagen, Denmark.ORCID http://orcid.org/0000-0002-2519-8127
Nicoline R AndersenDepartment of Nutrition, Exercise and Sports, University of Copenhagen, Copenhagen, Denmark.ORCID http://orcid.org/0000-0002-1512-2727
Per L MadsenDepartment of Nutrition, Exercise and Sports, University of Copenhagen, Copenhagen, Denmark.ORCID http://orcid.org/0000-0001-8655-4458
Jens J HolstDepartment of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.ORCID http://orcid.org/0000-0001-6853-3805
Sten MadsbadDepartment of Endocrinology, Hvidovre Hospital, Hvidovre, Denmark.ORCID http://orcid.org/0000-0002-5017-1815
Nils B JørgensenDepartment of Endocrinology, Hvidovre Hospital, Hvidovre, Denmark. nils.bruun.joergensen@regionh.dk.ORCID http://orcid.org/0000-0002-5764-6377

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aims/hypothesisSodium-glucose co-transporter 2 (SGLT2) inhibitors improve beta cell function in individuals with type 2 diabetes. It has been suggested this is due to relief of glucotoxicity, but the mechanism is unknown. The objective of the present study was to evaluate the effect of the SGLT2 inhibitor empagliflozin, compared with NPH insulin treatment, on beta cell function, and, secondarily, on insulin sensitivity.

methodsIn this open-label, randomised, cross-over study, 17 individuals with non-insulin-treated type 2 diabetes were randomised to receive 5 weeks of treatment with either empagliflozin or insulin titrated to a similar level of glycaemic control as with empagliflozin before crossing over to the other treatment. Key inclusion criteria included age ≥18 years, BMI ≥ 28 kg/m

resultsAll participants who completed the study were included in the analyses. With equipoised glycaemic control, insulin concentrations were higher during insulin treatment than during empagliflozin treatment. bGS and insulin sensitivity were higher during empagliflozin treatment than during insulin treatment. The disposition index thus improved during empagliflozin treatment compared with insulin treatment. CONCLUSIONS/

interpretationWith similar glycaemic control, insulin sensitivity was higher and beta cell function improved during empagliflozin compared with insulin treatment, possibly due to a disinhibitory effect of lower insulin concentrations.

trial registrationEudraCT 2017-002101-35.

fundingThis study was supported by Boehringer Ingelheim. Additional funding was provided by the Grosserer L.F. Foghts Fond, Charlottenlund, Denmark.

Indexed as

Benzhydryl CompoundsDiabetes Mellitus, Type 2GlucosidesHypoglycemic AgentsInsulinInsulin-Secreting CellsAdultAgedBlood GlucoseCross-Over StudiesFemaleHumansInsulin, IsophaneInsulin ResistanceMaleMiddle AgedBenzhydryl CompoundsBlood GlucoseempagliflozinGlucosidesHypoglycemic AgentsInsulinInsulin, IsophaneSodium-Glucose Transporter 2 InhibitorsBeta cell functionGlucotoxicityHyperinsulinaemiaInsulinSodium–glucose co-transporter 2 inhibitionType 2 diabetes

Identifiers

PMID41366535
PMCPMC12881062

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Registered trials

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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.