Yuan Yuan, Jiang Yong, Hu Chonghui, Wu Daixin, Chen Huimou, Tian Qing, He Rihua, Li Tingting, Huang Tianhao, Jiang Honghui, Zhong Wentao, Chen Yuan, Jiang Jiale, Zheng Shangyou, Chen Rufu
Guangdong Cardiovascular Institute, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, Guangdong, China.
Pancreas Center, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Southern Medical University, Guangzhou, Guangdong, China.
BMJ Open Gastroenterol. 2025 Jul 11;12(1):e001870. doi: 10.1136/bmjgast-2025-001870.
Liver diseases are established risk factors for hepatobiliary and pancreatic cancers. This study explores the relationship between liver disease and hepatobiliary-pancreatic cancers, focusing on transaminase levels and genetic susceptibility.
We conducted a large cohort study using data from 449 815 participants in the UK Biobank. Logistic regression models assessed cancer risks in liver disease versus control groups. The association between transaminase levels, polygenic risk scores (PRS), and hepatocellular carcinoma (HCC), intrahepatic cholangiocarcinoma (ICC), biliary tract cancer, and pancreatic cancer was examined. Two-sample Mendelian randomisation (MR) investigated the causal relationships between liver diseases and the four cancers.
Liver disease and elevated transaminase levels were significantly associated with increased cancer risks (p<0.001). Higher alanine transaminase and aspartate transaminase PRS were linked to increased HCC risk (HR=1.69, 95% CI 1.38 to 2.08; HR=1.79, 95% CI 1.46 to 2.19). MR analysis revealed a causal link between alcohol-associated liver disease (ALD) and both HCC (OR=1.379, 95% CI 1.109 to 1.714) and ICC (OR=1.429, 95% CI 1.130 to 1.807), while metabolic dysfunction-associated steatotic liver disease showed no significant associations.
Patients with liver diseases have a significantly higher risk of hepatobiliary and pancreatic cancers, and individuals with elevated transaminase levels also exhibit a genetic predisposition to HCC. ALD demonstrates significant causal relationships with HCC and ICC.
肝脏疾病是肝胆胰癌症已确定的风险因素。本研究探讨肝脏疾病与肝胆胰癌症之间的关系,重点关注转氨酶水平和遗传易感性。
我们使用英国生物银行中449815名参与者的数据进行了一项大型队列研究。逻辑回归模型评估了肝病组与对照组的癌症风险。研究了转氨酶水平、多基因风险评分(PRS)与肝细胞癌(HCC)、肝内胆管癌(ICC)、胆管癌和胰腺癌之间的关联。两样本孟德尔随机化(MR)研究了肝脏疾病与这四种癌症之间的因果关系。
肝脏疾病和转氨酶水平升高与癌症风险增加显著相关(p<0.001)。较高的丙氨酸转氨酶和天冬氨酸转氨酶PRS与HCC风险增加相关(HR=1.69,95%CI 1.38至2.08;HR=1.79,95%CI 1.46至2.19)。MR分析显示酒精性肝病(ALD)与HCC(OR=1.379,95%CI 1.109至1.714)和ICC(OR=1.429,95%CI 1.130至1.807)之间存在因果关系,而代谢功能障碍相关脂肪性肝病未显示出显著关联。
肝病患者患肝胆胰癌症的风险显著更高,转氨酶水平升高的个体也表现出对HCC的遗传易感性。ALD与HCC和ICC存在显著因果关系。