作者
Xiaodong Zhou,Seung Up Kim,Terry Cheuk‐Fung Yip,Salvatore Petta,Atsushi Nakajima,Emmanuel Tsochatzis,Jérôme Boursier,Elisabetta Bugianesi,Hannes Hagström,Wah‐Kheong Chan,Manuel Romero‐Gómez,José Luís Calleja,Victor de Lédinghen,Laurent Castéra,Arun J. Sanyal,George Boon‐Bee Goh,Philip N. Newsome,Jian‐Gao Fan,Michelle Lai,Céline Fournier‐Poizat,Hye Won Lee,Grace Lai‐Hung Wong,Angelo Armandi,Ying Shang,Grazia Pennisi,Elba Llop,Masato Yoneda,Marc de Saint-Loup,Clémence M. Canivet,Carmen Lara‐Romero,Rocío Gallego‐Durán,Amon Asgharpour,Kevin Kim‐Jun Teh,Sara Mahgoub,Mandy Sau-Wai Chan,Huapeng Lin,Wen‐Yue Liu,Giovanni Targher,Christopher D. Byrne,Vincent Wai‐Sun Wong,Ming‐Hua Zheng
摘要
Background Statins have multiple benefits in patients with metabolic-associated steatotic liver disease (MASLD). Aim To explore the effects of statins on the long-term risk of all-cause mortality, liver-related clinical events (LREs) and liver stiffness progression in patients with MASLD. Methods This cohort study collected data on patients with MASLD undergoing at least two vibration-controlled transient elastography examinations at 16 tertiary referral centres. Cox regression analysis was performed to examine the association between statin usage and long-term risk of all-cause mortality and LREs stratified by compensated advanced chronic liver disease (cACLD): baseline liver stiffness measurement (LSM) of ≥10 kPa. Liver stiffness progression was defined as an LSM increase of ≥20% for cACLD and from <10 kPa to ≥10 or LSM for non-cACLD. Liver stiffness regression was defined as LSM reduction from ≥10 kPa to <10 or LSM decrease of ≥20% for cACLD. Results We followed up 7988 patients with baseline LSM 5.9 kPa (IQR 4.6–8.2) for a median of 4.6 years. At baseline, 40.5% of patients used statins, and cACLD was present in 17%. Statin usage was significantly associated with a lower risk of all-cause mortality (adjusted HR=0.233; 95% CI 0.127 to 0.426) and LREs (adjusted HR=0.380; 95% CI 0.268 to 0.539). Statin usage was also associated with lower liver stiffness progression rates in cACLD (HR=0.542; 95% CI 0.389 to 0.755) and non-cACLD (adjusted HR=0.450; 95% CI 0.342 to 0.592), but not with liver stiffness regression (adjusted HR=0.914; 95% CI 0.778 to 1.074). Conclusions Statin usage was associated with a relatively lower long-term risk of all-cause mortality, LREs and liver stiffness progression in patients with MASLD.