Evidence map›Paper›PMID 41361413›Full record

ArticleScientific reports2025

Metabolic factors are associated with a higher risk of conventional adenoma in males during surveillance colonoscopy: findings from a South Australian cohort.

Meseret Derbew Molla, Erin L Symonds, Jean M Winter, Charles Cock, Molla M Wassie

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Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

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No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Meseret Derbew MollaCollege of Medicine and Public Health, Flinders Health and Medical Research Institute, Flinders University, Adelaide, South Australia. moll0130@flinders.edu.au.ORCID http://orcid.org/0000-0002-2622-522X
Erin L SymondsCollege of Medicine and Public Health, Flinders Health and Medical Research Institute, Flinders University, Adelaide, South Australia.
Jean M WinterCollege of Medicine and Public Health, Flinders Health and Medical Research Institute, Flinders University, Adelaide, South Australia.
Charles CockCollege of Medicine and Public Health, Flinders Health and Medical Research Institute, Flinders University, Adelaide, South Australia.
Molla M WassieCollege of Medicine and Public Health, Flinders Health and Medical Research Institute, Flinders University, Adelaide, South Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metabolic factors are associated with an increased risk of colorectal neoplasia, but whether metabolic factors impact individuals already considered at elevated risk of CRC due to a family or personal history of neoplasia is unknown. This study aimed to determine whether metabolic factors are associated with an increased risk of colorectal neoplasia in individuals undergoing surveillance colonoscopy in an Australian cohort. A retrospective cohort study design with a sample size of 2806 was implemented using colonoscopy and metabolic data from a hospital surveillance program. The association between self-reported metabolic factors (obesity, hypertension, type two diabetes (T2DM), dyslipidemia, and a cluster of these factors called metabolic syndrome (MetS)) and diagnosis of colorectal neoplasia, its advanced form, or histopathological subtypes at surveillance colonoscopy was analysed using logistic regression models. Metabolic factors that increased the odds of colorectal neoplasia diagnosis included obesity (adjusted odds ratio (AOR) = 1.61; 95% CI 1.06-2.44), T2DM (AOR = 1.40; 95% CI 1.09-1.80), and MetS (AOR = 1.47; 95%CI 1.10-1.99), with similar findings observed for the association with advanced colorectal neoplasia (obesity: AOR = 1.24; 95% CI 1.01-1.51; T2DM: AOR = 1.29; 95%CI 1.06-1.56; MetS: AOR = 1.45; 95% CI 1.18-1.80). These associations were driven by conventional adenomas (87% of all neoplasia) in males. No associations were observed between metabolic factors and colorectal neoplasia in females, nor for the odds of serrated polyps (p > 0.05). Obesity, T2DM and MetS were significant risk factors for the risk of conventional adenoma in a surveillance population, specifically in males. These metabolic disorders should be considered when determining the frequency of colonoscopy surveillance for males.

Indexed as

AdenomaColorectal NeoplasmsMetabolic SyndromeAdultAgedAustraliaColonoscopyDiabetes Mellitus, Type 2FemaleHumansMaleMiddle AgedObesityRetrospective StudiesRisk FactorsSouth AustraliaColorectal neoplasiaDiabetesMetabolic syndromeObesitySurveillance colonoscopy

Identifiers

PMID41361413
PMCPMC12796162

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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.