Moon Joon Ho, Jeong Seogsong, Jang Heejoon, Lee Dong Hyeon, Joo Sae Kyung, Koo Bo Kyung, Xia Qiang, Sha Meng, Chang Yoosoo, Kim Won
Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea; Division of Endocrinology and Metabolism, Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Department of Biomedical Informatics, Korea University College of Medicine, Seoul, Korea.
Clin Gastroenterol Hepatol. 2025 May 8. doi: 10.1016/j.cgh.2025.01.042.
We investigated the association between subtypes of steatotic liver disease (SLD) and 23 site-specific cancers in a nationwide cohort of young Korean adults.
From a nationwide health screening database in Korea, 2,877,245 young adults 20-39 years of age between 2013 and 2014 were included and followed up until December 31, 2022. Individuals were categorized into non-SLD, metabolic dysfunction-associated steatotic liver disease (MASLD), MASLD with increased alcohol intake (MetALD), and alcohol-associated liver disease (ALD) groups. Hepatic steatosis was defined as a fatty liver index ≥30. The primary outcome was all cancers, while secondary outcomes included 23 site-specific cancers. Cox proportional hazards regression models were used to estimate hazard ratios (HRs).
During 22,819,681 person-years of follow-up, 46,729 incident cancer cases developed. The MASLD (HR, 1.19; 95% confidence interval [CI], 1.16-1.22; P < .001) MetALD (HR, 1.12; 95% CI, 1.07-1.18; P < .001), and ALD (HR, 1.21; 95% CI, 1.12-1.31; P < .001) groups had a higher risk of all cancers compared with the non-SLD group. Most obesity-related cancers showed increased risk in individuals with either MASLD or MetALD. There was an increasing trend in all-cancer risk with increasing number of cardiometabolic risk factors among MASLD. Alcohol consumption had a modest effect on overall cancer risk, with varying effects on specific cancer types.
Young adults with MASLD, MetALD, or ALD are at increased risk of developing early-onset cancer.
我们在一个韩国年轻成年人的全国队列中,研究了脂肪性肝病(SLD)亚型与23种特定部位癌症之间的关联。
从韩国全国健康筛查数据库中,纳入了2013年至2014年间20 - 39岁的2877245名年轻成年人,并随访至2022年12月31日。个体被分为非SLD、代谢功能障碍相关脂肪性肝病(MASLD)、酒精摄入增加的MASLD(MetALD)和酒精性肝病(ALD)组。肝脂肪变性定义为脂肪肝指数≥30。主要结局是所有癌症,次要结局包括23种特定部位癌症。使用Cox比例风险回归模型来估计风险比(HRs)。
在22819681人年的随访期间,发生了46729例新发癌症病例。与非SLD组相比,MASLD组(HR,1.19;95%置信区间[CI],1.16 - 1.22;P <.001)、MetALD组(HR,1.12;95% CI,1.07 - 1.18;P <.001)和ALD组(HR,1.21;95% CI,1.12 - 1.31;P <.001)患所有癌症的风险更高。大多数与肥胖相关的癌症在患有MASLD或MetALD的个体中风险增加。在MASLD中,随着心血管代谢危险因素数量的增加,所有癌症的风险呈上升趋势。饮酒对总体癌症风险有适度影响,对特定癌症类型的影响各不相同。
患有MASLD、MetALD或ALD的年轻成年人患早发性癌症的风险增加。