Zhao Ming, Han Xinyu, Fan Hong, Liang Chenyu, Wang Haili, Zhang Xin, Zhao Shuzhen, Guo Chengnan, Liu Zhenqiu, Zhang Tiejun
Shanghai Institute of Infectious Disease and Biosecurity, School of Public Health, Fudan University, Shanghai, China.
Department of Epidemiology, School of Public Health, Fudan University, Shanghai, China.
Liver Int. 2025 Apr;45(4):e16136. doi: 10.1111/liv.16136. Epub 2024 Oct 18.
Metabolic dysfunction-associated steatotic liver disease (MASLD) is linked to various intrahepatic and extrahepatic diseases, but its association with severe infectious disease remains to be investigated.
We analysed data from the Shanghai Suburban Adult Cohort and Biobank, encompassing participants enrolled in 2016 and 2017 with available abdominal ultrasonography data, and followed them up until December 2022 (median follow-up = 5.71 years). We categorised the participants into the MASLD group and those without steatotic liver disease (non-SLD). Multivariable-adjusted Cox regression was used to estimate hazard ratios (HR) for severe infections in patients with MASLD compared to the non-SLD group. Cumulative incidences were calculated while accounting for competing risks (non-infection-related deaths). Mediation analyses were performed to explore the roles of cardiometabolic risk factors in the association between MASLD and severe infections.
Among the 33 072 eligible participants (mean age 56.37 years; 38.20% male), 11 908 (36.01%) were diagnosed with MASLD at baseline. Severe infections occurred in 912 (7.66%) MASLD patients and 1258 (5.94%) non-SLD. The rate of severe infections per 1000 person-years was higher in MASLD patients (13.58) than in comparators (10.48) (fully adjusted HR 1.18, 95% CI 1.07-1.30). The most frequent infections in MASLD were respiratory (7.25/1000 person-years) and urinary tract infections (2.61/1000 person-years). The 5-year cumulative incidence of severe infections was 6.79% (95% CI 6.36-7.26) in MASLD and 5.08% (95% CI 4.79-5.38) in comparators. Cardiometabolic risk factors, including waist circumference, triglycerides and HbA1C, partially mediate the association between MASLD and severe infections.
Patients with MASLD were at significantly higher risk of incident severe infections compared to the non-SLD group. Future studies are needed to elucidate the mechanisms linking MASLD to severe infections.
代谢功能障碍相关脂肪性肝病(MASLD)与多种肝内和肝外疾病相关,但其与严重感染性疾病的关联仍有待研究。
我们分析了上海郊区成人队列和生物样本库的数据,纳入了2016年和2017年登记且有可用腹部超声数据的参与者,并随访至2022年12月(中位随访时间 = 5.71年)。我们将参与者分为MASLD组和无脂肪性肝病(非SLD)组。采用多变量调整的Cox回归来估计MASLD患者与非SLD组相比发生严重感染的风险比(HR)。计算累积发病率时考虑了竞争风险(非感染相关死亡)。进行中介分析以探讨心脏代谢危险因素在MASLD与严重感染关联中的作用。
在33072名符合条件的参与者中(平均年龄56.37岁;38.20%为男性),11908名(36.01%)在基线时被诊断为MASLD。912名(7.66%)MASLD患者和1258名(5.94%)非SLD患者发生了严重感染。MASLD患者每1000人年的严重感染率(13.58)高于对照组(10.48)(完全调整后的HR为1.18,95%CI为1.07 - 1.30)。MASLD中最常见的感染是呼吸道感染(7.25/1000人年)和尿路感染(2.61/1000人年)。MASLD患者严重感染的5年累积发病率为6.79%(95%CI为6.36 - 7.26),对照组为5.08%(95%CI为4.79 - 5.38)。包括腰围、甘油三酯和糖化血红蛋白在内的心脏代谢危险因素部分介导了MASLD与严重感染之间的关联。
与非SLD组相比,MASLD患者发生严重感染的风险显著更高。未来需要开展研究以阐明MASLD与严重感染之间的关联机制。