Evidence map›Paper›PMID 42870927›Full record

SynthesisFrontiers in cardiovascular medicine2026

Cardiovascular outcomes of oral incretin-based drugs in type 2 diabetes: a GRADE-assessed meta-analysis of 67,679 patients.

Muhammad Faizan Ali, Omer Farooq Mohammed, Amina Suhail, Faisal Naseer, Nimra Shafi, Muhammad Usman Arshad, Omar Shazly, Muneeb Shad Mohmand, Husnain Ahmad, Noof K Binashikhbubkr and 5 more

Abstract readSystematic Review
In one paragraph

Synthesis in Frontiers in cardiovascular medicine, 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

15 authors.

Muhammad Faizan AliDepartment of Internal Medicine, HCA Healthcare Centerpoint Medical Center, Kansas City, MO, United States.
Omer Farooq MohammedFaculty of Medicine, Osmania Medical College, Hyderabad, India.
Amina SuhailDepartment of Medicine, Services Institute of Medical Sciences, Lahore, Pakistan.
Faisal NaseerDepartment of Medicine, Nishtar Medical University, Multan, Pakistan.
Nimra ShafiDepartment of Medicine, Arnot Ogden Medical Center, Elmira, NY, United States.
Muhammad Usman ArshadDepartment of Medicine, Shalamar Medical and Dental College, Lahore, Pakistan.
Omar ShazlyFaculty of Medicine, Ain Shams University, Cairo, Egypt.
Muneeb Shad MohmandDepartment of Medicine, Khyber Medical College, Peshawar, Pakistan.
Husnain AhmadDepartment of Medicine, Shalamar Medical and Dental College, Lahore, Pakistan.
Noof K BinashikhbubkrCollege of Medicine and Health Science, Hadhramout University, Hadhramout, Yemen.
Muhammad MaazDepartment of Medicine, Bacha Khan Medical College, Mardan, Pakistan.
Muhammad KhanDepartment of Medicine, Bacha Khan Medical College, Mardan, Pakistan.
Sivaram NeppalaDepartment of Cardiology, The University of Texas Health Science Center, San Antonio, TX, United States.
Mustafa Al-JarshawiNIHR Academy, National Institute for Health & Care Research, Leeds, United Kingdom.
Mohamed Fawzi HemidaDepartment of Internal Medicine, Alexandria Main University Hospital, Alexandria, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: While injectable GLP-1 receptor agonists like semaglutide have demonstrated clear cardiovascular benefits in type 2 diabetes mellitus (T2DM), the role of oral incretin-based therapies, including oral semaglutide and DPP-4 inhibitors-remains less well defined. Comprehensive evaluation of their cardiovascular efficacy is warranted. Research question: What are the cardiovascular outcomes associated with oral incretin-based therapies, specifically oral semaglutide and DPP-4 inhibitors, in patients with T2DM compared to placebo or standard care. Methods: We searched electronic databases for randomized controlled trials (RCTs). Meta-analysis was conducted in R version 4.4.3 using the "meta" and "metasens" packages. Statistical analysis was performed using R software and RStudio (version 4.4.2). We calculated pooled estimates using risk ratios (RR) with 95% confidence intervals (CIs). Results: A total of 9 studies comprising 67,679 patients were included, of which two evaluated oral semaglutide and the remaining seven assessed DPP-4 inhibitors. There was no significant reduction in all-cause mortality (RR 0.97, 95% CI 0.90-1.04, Conclusion: Oral incretin-based therapies were not associated with significant reductions in all-cause mortality, cardiovascular death, or MACE overall, though oral semaglutide showed a significant MACE benefit and reduced coronary revascularization on subgroup analysis. Non-fatal MI, fatal or non-fatal MI, non-fatal stroke, fatal or non-fatal stroke and hospitalization due to heart failure or unstable angina were unaffected, and oral semaglutide carried a higher risk of treatment discontinuation. These findings suggest no clear class-wide cardiovascular benefit of oral incretins, with signals specific to oral semaglutide warranting confirmation in dedicated trials. Systematic Review Registration: PROSPERO CRD420251113835.

Indexed as

cardiovascular diseasecardiovascular outcomesdiabetes mellitusincretin-based therapiesmeta-analysistype 2 diabetes mellitus

Identifiers

PMID42870927
PMCPMC13657929

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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.