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Long-Term Risk of Inflammatory Bowel Disease With MASLD: A Large-Scale Prospective Cohort Study in UK Biobank
Qian Zhang1, Fang Xu1, Zuyao Wang1
1Department of Gastroenterology, Beijing Friendship Hospital, Capital Medical University, National Clinical Research Center for Digestive Disease, Beijing Digestive Diseases Center, Beijing Key Laboratory for Precancerous Lesion of Digestive Disease, Beijing, China.
Metabolic dysfunction-associated steatotic liver disease (MASLD), including pure MASLD and MetALD, is linked to a higher risk of developing inflammatory bowel disease (IBD). The risk increases with more cardiometabolic risk factors present.
Area of Science:
- Hepatology and Gastroenterology
- Metabolic Disorders
- Epidemiology
Background:
- Global epidemics of metabolic dysfunction-associated steatotic liver disease (MASLD) and inflammatory bowel disease (IBD) are worsening.
- Understanding the link between MASLD and IBD is crucial for public health.
- Investigating the role of cardiometabolic risk factors (CMRFs) in this association is important.
Purpose of the Study:
- To prospectively examine the association between MASLD, its subtypes, and CMRFs with the long-term risk of incident IBD.
- To analyze the risk for specific IBD types, ulcerative colitis (UC) and Crohn's disease (CD).
- To determine if the number of CMRFs influences the risk of developing IBD.
Main Methods:
- Utilized UK Biobank data, including over 400,000 participants.
- Defined MASLD using fatty liver index and at least one CMRF, adhering to AASLD/EASL criteria.
- Classified MASLD into pure MASLD and MetALD (MASLD with increased alcohol intake).
- Employed multivariable Cox regression to analyze associations with incident IBD over a median 13.0-year follow-up.
Main Results:
- 37.6% of participants had MASLD at baseline.
- MASLD was significantly associated with a higher risk of incident IBD (HR=1.39), UC (HR=1.34), and CD (HR=1.51).
- Both pure MASLD and MetALD showed increased IBD risk.
- The risk of incident IBD progressively increased with a higher number of CMRFs (ptrend < 0.001).
Conclusions:
- MASLD, encompassing both pure MASLD and MetALD, is associated with an elevated risk of developing IBD, including UC and CD.
- The presence of multiple CMRFs amplifies the risk of incident IBD.
- These findings highlight the interconnectedness of metabolic health and gastrointestinal inflammatory conditions.
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