Lean individuals with metabolic-dysfunction associated steatotic liver disease and gastrointestinal cancers risk: A retrospective cohort study.
Abstract
811 Background: Lean individuals with MASLD may represent a distinct subgroup at increased risk for gastrointestinal cancers, though evidence from real-world data remains limited. This study aimed to investigate the association between lean MASLD and GI cancer incidence using a large, multicenter retrospective cohort. Methods: We performed a population-based retrospective cohort study utilizing the TriNetX network, which compiles de-identified electronic health records from healthcare institutions across the United States. Patients with MASLD were classified as lean or non-lean (BMI ≥ 25) and were compared accordingly. The primary outcomes were gastrointestinal cancers and their subtypes, evaluated over a 5-year follow-up period using Cox proportional hazards models. Results: After 1:1 propensity score matching on demographics, comorbidities, labs, and medication use, 34,663 patients remained in each group with comparable characteristics. Over 5 years, lean individuals with MASLD exhibited significantly higher incidence of overall GI cancer compared to non-lean individuals (2.2% vs. 1.4%; HR 1.66, 95% CI: 1.48–1.87). Elevated risks were observed for esophageal cancer (HR 3.00, 95% CI: 1.80–4.99), gastric cancer (HR 2.96, 95% CI: 2.00–4.37), pancreatic cancer (HR 2.55, 95% CI: 2.00–3.26), colorectal cancer (HR 1.53, 95% CI: 1.13–2.06), biliary tract cancer (HR 1.76, 95% CI: 1.16–2.67), and unspecified GI cancers (HR 2.03, 95% CI: 1.17–3.53). Liver cancer rates were similar between groups (HR 1.05, 95% CI: 0.85–1.31). Conclusions: Lean MASLD was associated with a significantly increased risk of several gastrointestinal cancers, underscoring the need for tailored cancer surveillance strategies in this vulnerable subgroup. 5-year incidence of clinical outcome in lean and non-lean metabolic dysfunction-associated steatotic liver disease. Outcome MASLD leanEvents N (%) MASLD non-leanEvents N (%) Hazard Ratio (95% CI) p-value Gastrointestinal cancer 709 (2.2%) 455 (1.4%) 1.66 (1.48−1.87) <0.001 Subtypes Esophageal cancer 57 (0.2%) 20 (0.1%) 3.00 (1.80−4.99) <0.001 Gastric cancer 96 (0.3%) 34 (0.1%) 2.96 (2.00−4.37) <0.001 Liver cancer 163 (0.5%) 162 (0.5%) 1.05 (0.85−1.31) 0.652 Colorectal cancer 104 (0.3%) 71 (0.2%) 1.53 (1.13−2.06) 0.006 Pancreatic cancer 223 (0.7%) 92 (0.3%) 2.55 (2.00−3.26) <0.001 Biliary tract cancer 59 (0.2%) 35 (0.1%) 1.76 (1.16−2.67) 0.007 Unspecified site gastrointestinal cancer 37 (0.1%) 19 (0.1%) 2.03 (1.17−3.53) 0.010 CI: confidence interval; HR: hazard ratio.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (10)
Pojsakorn Danpanichkul
Texas Tech University, Lubbock, Texas, United States
Yanfang Pang
Department of Microbiology, Chiang Mai University, Chiang Mai, Thailand
Donghee Kim
Global Science Research Center for Systems Chemistry
Hector Garcia Pleitez
1Texas Tech University Health Sciences Center, Department of Internal Medicine, Lubbock, United States
Xiaoyi Zhang
J. Drew Payne
Department of Medicine, Texas Tech University Health Sciences Center, Lubbock, TX
Kanak Das
Division of Gastroenterology, Texas Tech University Health Sciences Center, Lubbock, TX
Karn Wijarnpreecha
Amit Singal
Department of Internal Medicine, UT Southwestern Medical Center, Dallas, TX
Ju Dong Yang