Evidence map›Paper›PMID 42614039›Full record

SynthesisEndocrinology, diabetes & metabolism2026

Efficacy of Telmisartan in MASLD/NAFLD: A Systematic Review and Meta-Analysis of Randomized Controlled Trials.

Shayan Shojaei, Dorsa Shekouh, Asma Mousavi, Salma Rostamipourfard, Saeed Karami, Salar Azadnik, Salma Nozhat, Seyed Alireza Mirhosseini, Erfan Hashemi, Noureen Fatima and 3 more

Abstract readSystematic ReviewMeta-AnalysisReview
In one paragraph

Synthesis in Endocrinology, diabetes & metabolism, 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

13 authors.

Shayan ShojaeiCardiovascular Diseases Research Institute, Tehran University of Medical Sciences, Tehran, Iran.ORCID https://orcid.org/0000-0002-2614-2467
Dorsa ShekouhCardiovascular Research Center, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.ORCID https://orcid.org/0000-0001-7340-4805
Asma MousaviCardiovascular Diseases Research Institute, Tehran University of Medical Sciences, Tehran, Iran.ORCID https://orcid.org/0000-0002-8419-779X
Salma RostamipourfardCardiovascular Research Center, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.ORCID https://orcid.org/0000-0003-4906-6804
Saeed KaramiCardiovascular Research Center, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.ORCID https://orcid.org/0009-0005-6367-850X
Salar AzadnikDepartment of Internal Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.ORCID https://orcid.org/0000-0002-6825-5312
Salma NozhatDepartment of Cardiology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
Seyed Alireza MirhosseiniCardiovascular Research Center, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.ORCID https://orcid.org/0009-0000-3920-8640
Erfan HashemiDepartment of Surgery, University of Calgary, Alberta, Canada.ORCID https://orcid.org/0000-0002-9119-5143
Noureen FatimaDepartment of Medicine, Gujranwala Teaching Hospital, Gujranwala, Pakistan.ORCID https://orcid.org/0009-0000-3607-1167
Ali Fatehi HassanabadDepartment of Cardiac Sciences, Section of Cardiac Surgery, Libin Cardiovascular Institute, University of Calgary, Cumming School of Medicine, Calgary, Alberta, Canada.ORCID https://orcid.org/0000-0003-0650-0260
Mahsa BorjzadehgashtasebDepartment of Cardiology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.ORCID https://orcid.org/0009-0009-4060-5593
Alireza ArzhangzadehDepartment of Cardiology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.ORCID https://orcid.org/0000-0002-7466-7487

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundActivation of the renin-angiotensin-aldosterone system contributes to hepatic inflammation in metabolic dysfunction-associated steatotic liver disease (MASLD). Telmisartan, an angiotensin II receptor blocker with partial PPAR-γ agonistic activity, has been hypothesized to confer metabolic benefits; however, current clinical evidence has not consistently demonstrated such effects.

aimThis systematic review and meta-analysis evaluated the efficacy of telmisartan on metabolic, biochemical, and histological outcomes in MASLD.

methodsElectronic databases (PubMed, Embase, Web of Science, Scopus) were searched through 2026 for randomized controlled trials (RCTs) investigating telmisartan in adults with MASLD. Risk of bias was assessed using the RoB2 tool. Random-effects meta-analyses calculated pooled mean differences (MDs) with 95% confidence intervals (CIs).

resultsSix RCTs comprising 258 participants (126 telmisartan, 132 controls) met the inclusion criteria. Telmisartan treatment was associated with a modest reduction in fasting blood sugar compared with controls (MD = -2.78 mg/dL; 95% CI -5.17 to -0.39; p = 0.023); however, this finding was accompanied by substantial heterogeneity (I

conclusionCurrent evidence does not demonstrate consistent metabolic, biochemical, or histological benefits of telmisartan in MASLD. Although a modest reduction in fasting blood glucose was observed, substantial between-study heterogeneity and the modest effect size limit confidence in this finding.

Indexed as

Angiotensin II Type 1 Receptor BlockersMetabolic DiseasesNon-alcoholic Fatty Liver DiseaseTelmisartanHumansRandomized Controlled Trials as TopicTreatment OutcomeAngiotensin II Type 1 Receptor BlockersTelmisartanMASLDmeta‐analysistelmisartan

Identifiers

PMID42614039
PMCPMC13487458

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.