Evidence map›Paper›PMID 39980820›Full record

ReviewHealth science reports2025

Association Between GLP1 RAs Use and Risk of Colorectal Cancer: A Systematic Review and Meta-Analysis.

Ganesh Bushi, Shilpa Gaidhane, Suhas Ballal, Sanjay Kumar, Mahakshit Bhat, Shilpa Sharma, M Ravi Kumar, Aashna Sinha, Mahalaqua Nazli Khatib, Nishant Rai and 3 more

Abstract readReview
In one paragraph

Review in Health science reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–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

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
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  4. Article
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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

13 authors.

Ganesh BushiCenter for Global Health Research, Saveetha Medical College and Hospital, Saveetha Institute of Medical and Technical Sciences Saveetha University Chennai Tamil Nadu India.ORCID https://orcid.org/0000-0002-0397-7904
Shilpa GaidhaneOne Health Centre, Jawaharlal Nehru Medical College, Datta Meghe Institute of Higher Education Wardha Maharashtra India.
Suhas BallalDepartment of Chemistry and Biochemistry, School of Sciences JAIN (Deemed to be University) Bangalore Karnataka India.
Sanjay KumarDepartment of Allied Healthcare and Sciences Vivekananda Global University Jaipur Rajasthan India.
Mahakshit BhatDepartment of Medicine, National Institute of Medical Sciences NIMS University Rajasthan Jaipur Rajasthan India.
Shilpa SharmaChandigarh Pharmacy College, Chandigarh Group of Colleges-Jhanjeri Mohali Punjab India.
M Ravi KumarDepartment of Chemistry Raghu Engineering College Visakhapatnam Andhra Pradesh India.
Aashna SinhaUttaranchal Institute of Pharmaceutical Sciences, Division of Research and Innovation Uttaranchal University Dehradun Uttarakhand India.
Mahalaqua Nazli KhatibDivision of Evidence Synthesis, Global Consortium of Public Health and Research, Datta Meghe Institute of Higher Education Wardha Maharashtra India.
Nishant RaiDepartment of Biotechnology Graphic Era (Deemed to be University) Dehradun Uttarakhand India.
Sanjit SahSR Sanjeevani Hospital Kalyanpur Siraha Nepal.ORCID 0009-0008-5017-083X
Sorabh LakhanpalSchool of Pharmaceutical Sciences Lovely Professional University Phagwara Punjab India.
Muhammed ShabilUniversity Center for Research and Development, Chandigarh University Mohali Punjab India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Objective: As the global prevalence of type 2 diabetes mellitus (T2DM) continues to rise, addressing its associated health risks, including colorectal cancer (CRC), is important. This study examines the relationship between the use of glucagon-like peptide-1 receptor agonists (GLP-1RAs) and the risk of CRC in comparison with other antidiabetic therapies. Methods: We conducted a systematic search of PubMed, Embase, and Web of Science up to August 10, 2024, following PRISMA guidelines. Data extraction and screening were performed using Nested Knowledge software. Meta-analysis random effect model pooled Risk ratios (RRs) calculated using was performed using R v4.4 statistical software g. The protocol was registered with PROSPERO. Results: Out of 1825 identified studies, five met the inclusion criteria, involving 2,047,256 T2DM patients assessing CRC risk. GLP-1RAs were associated with a significant reduction in CRC risk compared to thiazolidinediones (RR: 0.82, 95% CI: 0.68-0.96), insulin (RR: 0.57, 95% CI: 0.32-0.81), and SGLT2 inhibitors (RR: 0.77, 95% CI: 0.59-0.95). Comparisons with sulfonylureas, DPP-4 inhibitors, and metformin were not statistically significant. A potential protective effect against alpha-glucosidase inhibitors was observed (RR: 0.59, 95% CI: 0.18-1.00) but requires further investigation. Conclusion: The use of GLP-1RAs in T2DM is linked to a reduced risk of CRC compared to several standard antidiabetic therapies. These findings underscore the importance of considering long-term cancer risks in diabetes management and highlight the need for continued research to fully understand the implications of GLP-1RA use in T2DM patients.

Indexed as

colorectal cancerglucagon‐like peptide‐1 receptor agonistsmeta‐analysissystematic review

Identifiers

PMID39980820
PMCPMC11839483

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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.