The University of Southampton
University of Southampton Institutional Repository

Colorectal cancer in metabolic dysfunction-associated steatotic liver disease: an international Delphi consensus statement

Colorectal cancer in metabolic dysfunction-associated steatotic liver disease: an international Delphi consensus statement
Colorectal cancer in metabolic dysfunction-associated steatotic liver disease: an international Delphi consensus statement
Background: metabolic dysfunction-associated steatotic liver disease (MASLD) is the most common chronic liver disease worldwide. Epidemiological evidence indicates that MASLD is associated with an increased risk of developing colorectal cancer (CRC). MASLD and CRC share many common risk factors and pathophysiological mechanisms, but an optimal strategy for identifying and managing CRC risk in individuals with MASLD remains lacking.

Objective: this study aimed to achieve consensus on the risk of CRC in individuals with MASLD.

Design: a Delphi survey was conducted by a multidisciplinary panel of 35 international experts from diverse medical fields across Asia, Europe, North America, South America, Oceania and Africa. Experts evaluated 17 statements across three domains: epidemiology, pathogenesis and management.

Results: consensus was achieved on all 17 statements. MASLD is associated with an increased risk of CRC, and metabolic burden further increases this risk. Furthermore, the severity of MASLD is associated with worse outcomes in patients with MASLD and CRC. The gut–liver axis and gut dysbiosis play key roles in the development of MASLD and CRC, while leptin and adiponectin may also be involved. Weight loss with lifestyle interventions, early CRC screening, bariatric surgery and use of GLP-1 receptor agonists are highlighted as potential risk-reduction strategies.

Conclusion: the expert panel emphasises the need for greater clinical vigilance for CRC among individuals with MASLD. This consensus supports a paradigm shift towards earlier, risk-adapted screening and integrated metabolic management to reduce the burden of CRC in the MASLD population.



1468-3288
Wu, Chu-Tian
3f6b6506-ab76-477c-a8ec-e15a32ef09d3
Targher, Giovanni
e1e486a5-9203-443e-b91f-61ef88a7aa45
Byrne, Chrisopher D.
1370b997-cead-4229-83a7-53301ed2a43c
Younossi, Zobair M.
cefccab7-0806-4dab-8ba6-2e39d9577bbc
Armstrong, Matthew J.
ccf2b72f-884a-45af-b8f1-1a706d525bca
et al.
Wu, Chu-Tian
3f6b6506-ab76-477c-a8ec-e15a32ef09d3
Targher, Giovanni
e1e486a5-9203-443e-b91f-61ef88a7aa45
Byrne, Chrisopher D.
1370b997-cead-4229-83a7-53301ed2a43c
Younossi, Zobair M.
cefccab7-0806-4dab-8ba6-2e39d9577bbc
Armstrong, Matthew J.
ccf2b72f-884a-45af-b8f1-1a706d525bca

Wu, Chu-Tian, Targher, Giovanni and Byrne, Chrisopher D. , et al. (2026) Colorectal cancer in metabolic dysfunction-associated steatotic liver disease: an international Delphi consensus statement. Gut. (doi:10.1136/gutjnl-2025-337374).

Record type: Article

Abstract

Background: metabolic dysfunction-associated steatotic liver disease (MASLD) is the most common chronic liver disease worldwide. Epidemiological evidence indicates that MASLD is associated with an increased risk of developing colorectal cancer (CRC). MASLD and CRC share many common risk factors and pathophysiological mechanisms, but an optimal strategy for identifying and managing CRC risk in individuals with MASLD remains lacking.

Objective: this study aimed to achieve consensus on the risk of CRC in individuals with MASLD.

Design: a Delphi survey was conducted by a multidisciplinary panel of 35 international experts from diverse medical fields across Asia, Europe, North America, South America, Oceania and Africa. Experts evaluated 17 statements across three domains: epidemiology, pathogenesis and management.

Results: consensus was achieved on all 17 statements. MASLD is associated with an increased risk of CRC, and metabolic burden further increases this risk. Furthermore, the severity of MASLD is associated with worse outcomes in patients with MASLD and CRC. The gut–liver axis and gut dysbiosis play key roles in the development of MASLD and CRC, while leptin and adiponectin may also be involved. Weight loss with lifestyle interventions, early CRC screening, bariatric surgery and use of GLP-1 receptor agonists are highlighted as potential risk-reduction strategies.

Conclusion: the expert panel emphasises the need for greater clinical vigilance for CRC among individuals with MASLD. This consensus supports a paradigm shift towards earlier, risk-adapted screening and integrated metabolic management to reduce the burden of CRC in the MASLD population.



Text
Manuscript_gut - Accepted Manuscript
Available under License Creative Commons Attribution.
Download (177kB)
Text
Supplementary - Accepted Manuscript
Available under License Creative Commons Attribution.
Download (17kB)
Image
Figure 1 - Accepted Manuscript
Available under License Creative Commons Attribution.
Download (1MB)
Image
Figure 2 - Accepted Manuscript
Available under License Creative Commons Attribution.
Download (1MB)
Image
Figure 3 - Accepted Manuscript
Available under License Creative Commons Attribution.
Download (6MB)

Show all 5 downloads.

More information

Accepted/In Press date: 12 January 2026
e-pub ahead of print date: 21 January 2026

Identifiers

Local EPrints ID: 509513
URI: http://eprints.soton.ac.uk/id/eprint/509513
ISSN: 1468-3288
PURE UUID: 48843be0-d8e3-4c39-ab23-16d04570837c
ORCID for Chrisopher D. Byrne: ORCID iD orcid.org/0000-0001-6322-7753

Catalogue record

Date deposited: 24 Feb 2026 17:55
Last modified: 07 Mar 2026 02:49

Export record

Altmetrics

Contributors

Author: Chu-Tian Wu
Author: Giovanni Targher
Author: Zobair M. Younossi
Author: Matthew J. Armstrong
Corporate Author: et al.

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×