← Issue №11/ week of Sep 13, 2026/ the whole section, in full

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Colorectal guideline · Sep 7, 2026 · Gut · IF 24.6

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

Guideline / reviewMASLDcolorectal cancercolorectal cancer screeningguideline
Clinical takeawayHeighten CRC surveillance in MASLD patients; screening intensity should be informed by MASLD severity (worse outcomes with advanced disease), though specific severity-based intervals are not defined in this consensus. Coordinate with hepatology for risk-adapted screening strategy. Include metabolic management (weight loss, GLP-1 agonists where indicated, bariatric surgery where eligible); no proven CRC risk-reduction benefit from these interventions in MASLD is presented.
What it foundDelphi consensus: MASLD associates with increased CRC risk; severity of MASLD is associated with worse CRC outcomes, and metabolic burden further increases risk. Risk stratification by MASLD severity grade is not specified in this consensus. Quantitative risk elevation not specified.
ContextConfirms epidemiological association between MASLD and elevated CRC risk. Severity of MASLD is associated with worse CRC outcomes, suggesting it should inform surveillance strategy, but severity-based risk categories for screening are not defined. Expert agreement on gut-liver axis and dysbiosis provides mechanistic plausibility without clinical thresholds. Current practice applies standard CRC risk stratification without MASLD-specific adjustment.
Emergingsuggested applicable standard· American Association for the Study of Liver Diseases (AASLD), "AASLD Practice Guidance on the clinical assessment and management of nonalcoholic fatty liver disease," Hepatology 2023;77(5):1797-1835 (with the October 2024 resmetirom and November 2025 semaglutide Practice Guidance updates)

Decision at stakeCRC screening strategy and intensity for patients with MASLD

No single passage of this standard matched the paper closely enough to quote, so none is shown. The standard is cited above.

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Lifestyle modification is the foundation of MASLD treatment, centered on a tiered weight-loss ladder targeting 7-10% body-weight loss for NASH/fibrosis improvement via a Mediterranean dietary pattern, elimination of sugar-sweetened beverages, 150 min/week of moderate aerobic activity plus resistance training, and alcohol reduction toward abstinence. Pharmacotherapy and bariatric surgery are added on top of lifestyle when lifestyle alone is insufficient, but each is gated by disease stage, comorbidity, and eligibility rather than applied as generic escalation: resmetirom is indicated (in conjunction with diet and exercise) only for noncirrhotic MASH with moderate-to-advanced fibrosis (F2-F3) and is not recommended in cirrhosis; GLP-1 receptor agonists are directed to patients with coexisting type 2 diabetes and/or obesity, with semaglutide now guidance-supported for noncirrhotic MASH with F2-F3 fibrosis; pioglitazone is reserved for biopsy-proven MASH, with or without type 2 diabetes; vitamin E 800 IU/day is reserved for biopsy-proven MASH in patients without type 2 diabetes and without cirrhosis; and bariatric/metabolic surgery is an option only for patients meeting metabolic weight-loss-surgery eligibility (BMI ≥40 kg/m2, or ≥35 kg/m2 with comorbidities), cannot be considered primary therapy for compensated MASH cirrhosis, and carries increased operative risk in decompensated cirrhosis. Comorbidity management-CV risk, statins, diabetes, OSA screening, thyroid, vaccination-is integral to MASLD care.

American Association for the Study of Liver Diseases (AASLD), "AASLD Practice Guidance on the clinical assessment and management of nonalcoholic fatty liver disease," Hepatology 2023;77(5):1797-1835 (with the October 2024 resmetirom and November 2025 semaglutide Practice Guidance updates) · reviewed 2026-07-23 ↗
Wu CT … Zheng MH · Gut · IF 24.6 · PubMed ↗Permalink
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