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Association of metabolic dysfunction‐associated fatty liver disease with gallstone development: A longitudinal study

医学 优势比 内科学 脂肪肝 代谢综合征 胆结石 置信区间 胃肠病学 疾病 内分泌学 肥胖
作者
Masahiro Sogabe,Toshiya Okahisa,Miwako Kagawa,Motoko Sei,Kaizo Kagemoto,Hironori Tanaka,Yoshifumi Kida,Fumika Nakamura,Tetsu Tomonari,Koichi Okamoto,Hiroshi Miyamoto,Yasushi Sato,Masahiko Nakasono,Tetsuji Takayama
出处
期刊:Journal of Gastroenterology and Hepatology [Wiley]
卷期号:39 (4): 754-761 被引量:2
标识
DOI:10.1111/jgh.16483
摘要

Abstract Background and Aim The influence of metabolic dysfunction‐associated fatty liver disease on gallstone development remains unclear. We aimed to investigate the longitudinal association between metabolic dysfunction‐associated fatty liver disease and gallstone development in both men and women. Methods This observational cohort study included 5398 patients without gallstones who underwent > 2 health check‐ups between April 1, 2014, and March 31, 2020. A generalized estimation equation model was used to analyze the association between metabolic dysfunction‐associated fatty liver disease and gallstone development according to repeated measures at baseline and most recent stage. Results After adjustment, the odds ratios of metabolic dysfunction‐associated fatty liver disease for gallstone development in men and women were 3.019 (95% confidence interval [CI]: 1.901–4.794) and 2.201 (95% CI: 1.321–3.667), respectively. Among patients aged ≥ 50 years, the odds ratio for gallstone development was significantly enhanced with increasing metabolic dysfunction‐associated fatty liver disease component numbers in both sexes; however, no significance was observed in those aged < 50 years. Other significant risk factors for gallstone development were age (odds ratio: 1.093, 95% CI: 1.060–1.126) and waist circumference (odds ratio: 1.048, 95% CI: 1.018–1.079) in men and age (odds ratio: 1.035, 95% CI: 1.003–1.067) and current smoking (odd ratio: 5.465, 95% CI: 1.881–15.88) in women. Conclusion Although the risk factors for gallstone development differed between sexes, metabolic dysfunction‐associated fatty liver disease was common. Paying attention to an increase in the number of metabolic dysfunction‐associated fatty liver disease components in patients aged ≥ 50 years is important for gallstone prevention.

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