Evidence map›Paper›PMID 40486129›Full record

ArticleClinical hypertension2025

The impact of renin-angiotensin system inhibitors on colorectal neoplasm development.

Yoo Min Han, Ji Min Choi, Tae-Min Rhee, Su-Yeon Choi, Heesun Lee

Abstract read
In one paragraph

Article in Clinical hypertension, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Yoo Min HanDivision of Gastroenterology, Department of Internal Medicine, Seoul National University Hospital Healthcare System Gangnam Centre, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0001-5580-8427
Ji Min ChoiDivision of Gastroenterology, Department of Internal Medicine, Seoul National University Hospital Healthcare System Gangnam Centre, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0001-8611-4647
Tae-Min RheeDivision of Cardiology, Department of Internal Medicine, Seoul National University Hospital Healthcare System Gangnam Centre, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0002-0504-0736
Su-Yeon ChoiDivision of Cardiology, Department of Internal Medicine, Seoul National University Hospital Healthcare System Gangnam Centre, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0001-9977-4740
Heesun LeeDivision of Cardiology, Department of Internal Medicine, Seoul National University Hospital Healthcare System Gangnam Centre, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0003-4037-3955

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Renin-angiotensin system (RAS) inhibitors have shown potential chemopreventive effects against colorectal cancer (CRC). However, little is known about the impact of RAS inhibitors on the risk of colorectal precancerous lesions. Methods: Preclinically, we established mouse models of colitis-associated colon cancer and xenografts: vehicle, 1 mg/kg, 5 mg/kg enalapril groups. Body weight, colon length, and colorectal tumor size were evaluated on the euthanization day. Clinically, we retrospectively recruited 8,388 asymptomatic adults undergoing their first-ever colonoscopy for health check-ups (index cohort). From the index cohort, we selected individuals undergoing follow-up colonoscopy (follow-up cohort). The study outcome was incidental and recurrent colorectal neoplasms, including CRC. We evaluated the prevalence and risk of colorectal neoplasms associated with RAS inhibitor use of ≥ 1 year. Results: In the experimental study, enalapril administration significantly attenuated weight loss and colon shortening, reduced tumor numbers in colitis-associated colon cancer models, and decreased tumor volume in the xenografts. In the index cohort, while the initial analysis showed a positive association with the RAS inhibitor use (unadjusted odds ratio [OR], 1.22), this shifted toward an inverse trend after adjusting for confounders (adjusted OR, 0.91). During follow-up (median, 41.0 months), incidental and recurrent colorectal neoplasms were less common in the RAS inhibitor group (32.6%) than in the other anti-hypertensives group (39.1%) ( Conclusions: Long-term, regular use of RAS inhibitors independently reduces the risk of colorectal neoplasms, irrespective of dosage or drug type. Given their potential chemopreventive effects on colorectal neoplasms, RAS inhibitors may serve as a preventive strategy starting from the precancerous stage.

Indexed as

ChemopreventionColorectal cancerRAS inhibitorTranslational research

Identifiers

PMID40486129
PMCPMC12145888

What Socratic holds

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LicenceCC BY-NC
Read underepoch 390

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 Socratic graph.