IF 12.9 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Tzu-I Chen, Ming-Huang Chen, Szu-Ching Yin, Chih-Jo Lin, Tram Kim Lam, Chia-Wei Huang, Yi-Ting Chen, Xia-Rong Liu, Yun-Zheng Gao, Wan-Lun Hsu, Hsuan-Yu Chen, Ta-Sen Yeh, Jill Koshiol, Mei-Hsuan Lee
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引用次数: 0

摘要

背景和目的:这是一项基于人群的大规模队列研究:这项基于人群的大规模队列研究探讨了代谢综合征与胆管癌(包括肝内和肝外胆管癌)风险之间的关系:共有 4,932,211 名年龄≥40 岁的成年人参加了政府发起的健康体检项目(2012-2017 年),该项目收集了生活方式数据、人体测量数据和生化检验数据。随访一直持续到2021年,并与国家癌症和死亡登记处进行数据连接,以确定胆管癌的发生率并获得生命状态信息。Fine 和 Gray 模型考虑了竞争风险。在 35,879,371 人年的随访期间,共发现 6,117 例胆管癌病例,发病率为每 100,000 人年 17.05 例(95% CI:15.90-18.20)。患有代谢综合征的人肝内和肝外胆管癌的发病率都明显较高(P结论:代谢综合征与胆管癌风险之间的正相关表明,控制代谢风险因素可减少肝内和肝外胆管癌的发生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Associations between metabolic syndrome and cholangiocarcinoma risk: A large-scale population-based cohort study.

Background and aims: This large-scale, population-based cohort study examined the associations between metabolic syndrome and cholangiocarcinoma risk, including its intra- and extra-hepatic forms.

Approach and results: A total of 4,932,211 adults aged ≥40 years participated in a government-initiated health checkup program (2012-2017), which collected lifestyle data, anthropometric measurements, and biochemical tests. Follow-up continued until 2021, with data linkage to National Cancer and Death Registries to ascertain the occurrence of cholangiocarcinoma and obtain vital status information. Fine and Gray models accounted for competing risks. During 35,879,371 person-years of follow-up, 6,117 cholangiocarcinoma cases were identified, with an incidence rate of 17.05 (95% CI: 15.90-18.20) per 100,000 person-years. Individuals with metabolic syndrome had significantly higher incidences of both intra- and extra-hepatic cholangiocarcinoma (p<0.0001). The multivariate-adjusted hazard ratio (HR) for cholangiocarcinoma among those with metabolic syndrome was 1.20 (1.14-1.27). Stratification analyses by age, sex, liver enzyme levels, and comorbidities consistently demonstrated an increased cholangiocarcinoma risk among individuals with metabolic syndrome. A dose-response relationship was observed, with a higher number of metabolic components correlating with an elevated cholangiocarcinoma risk, even after accounting for all-cause mortality as a competing risk. The adjusted subdistribution HRs ranged from 1.16 (95% CI: 1.02-1.32) for individuals with one metabolic component to 1.67 (95% CI: 1.45-1.94) for those with five (p for trend <0.0001).

Conclusions: The positive association between metabolic syndrome and cholangiocarcinoma risk suggests that managing metabolic risk factors might reduce the occurrence of both intra- and extra-hepatic cholangiocarcinoma.

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来源期刊
Hepatology
Hepatology 医学-胃肠肝病学
CiteScore
27.50
自引率
3.70%
发文量
609
审稿时长
1 months
期刊介绍: HEPATOLOGY is recognized as the leading publication in the field of liver disease. It features original, peer-reviewed articles covering various aspects of liver structure, function, and disease. The journal's distinguished Editorial Board carefully selects the best articles each month, focusing on topics including immunology, chronic hepatitis, viral hepatitis, cirrhosis, genetic and metabolic liver diseases, liver cancer, and drug metabolism.
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