Evidence map›Paper›PMID 42440238›Full record

ArticleJournal of endocrinological investigation2026

Comparative effectiveness of subcutaneous GLP-1 receptor agonists versus SGLT2 inhibitors on metabolic and hepatic outcomes in T2DM with MASLD: a propensity score-matched study.

Barbara Toffoli, Matteo Sirignano, Valeria Bonato, Giulia Fusaro, Erica Russo, Valerio Velardi, Lory Saveria Crocè, Bruno Fabris, Riccardo Candido, Stella Bernardi

Abstract readComparative Study
In one paragraph

Article in Journal of endocrinological investigation, 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

10 authors.

Barbara ToffoliDepartment of Medical Surgical and Health Sciences, University of Trieste, Ospedale Di Cattinara 447, 34149, Trieste, Italy.
Matteo SirignanoDepartment of Medical Surgical and Health Sciences, University of Trieste, Ospedale Di Cattinara 447, 34149, Trieste, Italy.
Valeria BonatoDepartment of Medical Surgical and Health Sciences, University of Trieste, Ospedale Di Cattinara 447, 34149, Trieste, Italy.
Giulia FusaroDepartment of Medical Surgical and Health Sciences, University of Trieste, Ospedale Di Cattinara 447, 34149, Trieste, Italy.
Erica RussoDepartment of Medical Surgical and Health Sciences, University of Trieste, Ospedale Di Cattinara 447, 34149, Trieste, Italy.
Valerio VelardiDepartment of Medical Surgical and Health Sciences, University of Trieste, Ospedale Di Cattinara 447, 34149, Trieste, Italy.
Lory Saveria CrocèDepartment of Medical Surgical and Health Sciences, University of Trieste, Ospedale Di Cattinara 447, 34149, Trieste, Italy.
Bruno FabrisDepartment of Medical Surgical and Health Sciences, University of Trieste, Ospedale Di Cattinara 447, 34149, Trieste, Italy.
Riccardo Candido *Department of Medical Surgical and Health Sciences, University of Trieste, Ospedale Di Cattinara 447, 34149, Trieste, Italy.
Stella Bernardi *Department of Medical Surgical and Health Sciences, University of Trieste, Ospedale Di Cattinara 447, 34149, Trieste, Italy. stella.bernardi@asugi.sanita.fvg.it.ORCID http://orcid.org/0000-0002-7429-3075

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsMetabolic dysfunction-associated steatotic liver disease (MASLD) frequently coexists with type 2 diabetes mellitus (T2DM), complicating its management. In this population, we aimed to compare the effectiveness of subcutaneous GLP-1 receptor agonists (scGLP-1RA) to SGLT2 inhibitors (SGLT2i) on metabolic and hepatic parameters, while investigating the influence of GLP1R and PNPLA3 genetic variants on treatment response.

methodsThis retrospective study included patients with T2DM starting scGLP-1RA or SGLT2i, balanced through Propensity Score Matching (PSM) to account for baseline clinical differences. Clinical and biochemical data were compared at baseline and after one year of treatment. Genotyping was performed for PNPLA3 (rs738409) and GLP1R (rs761387, rs6923761) polymorphisms. Multivariable linear regression was used to identify independent predictors of HbA1c, BMI, and transaminase reduction.

resultsBoth drug classes significantly improved glycemic control and BMI. However, scGLP-1RA demonstrated superior efficacy in HbA1c and BMI reduction compared to SGLT2i (β = -0.349, p = 0.001; β = -0.711, p = 0.045). In MASLD subgroups (baseline ALT > 35 U/L or hepatic steatosis), only scGLP-1RA led to a significant reduction in ALT levels (p = 0.02). Multivariable analysis identified the GLP1R rs761387 G allele as an independent predictor of a blunted glycemic response (β = -0.277, p = 0.018).

conclusionsIn a real-world setting, scGLP-1RA showed higher potency than SGLT2i on metabolic and hepatic parameters. These findings support the preferential use of scGLP-1RA in patients with T2DM and MASLD and are consistent with current international recommendations. The association between GLP1R rs761387 variant and HbA1c reduction sheds light on the impact of this variant on treatment response. Further studies are needed to validate this genetic predictor in broader populations.

Indexed as

Diabetes Mellitus, Type 2Fatty LiverGlucagon-Like Peptide-1 Receptor AgonistsSodium-Glucose Transporter 2 InhibitorsAgedBiomarkersBlood GlucoseFemaleFollow-Up StudiesGlucagon-Like Peptide-1 ReceptorGlycated HemoglobinHumansHypoglycemic AgentsMaleMiddle AgedPrognosisBiomarkersBlood GlucoseGLP1R protein, humanGlucagon-Like Peptide-1 ReceptorGlucagon-Like Peptide-1 Receptor AgonistsGlycated Hemoglobinhemoglobin A1c protein, humanHypoglycemic AgentsSodium-Glucose Transporter 2 InhibitorsALTGLP-1RALIVERMASLDrs761387SGLT2iSNPT2DM

Identifiers

PMID42440238
PMCPMC13627211

What OpenQuestion 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 OpenQuestion graph.