Long-term liver-related outcomes and liver stiffness progression of statin usage in steatotic liver disease
Authors
Xiao-Dong 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-Gomez ; José Luis Calleja ; Victor de Lédinghen ; Laurent Castéra ; Arun J Sanyal ; George Boon-Bee Goh ; Philip N Newsome ; Jiangao 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 ; Clemence M Canivet ; Carmen Lara-Romero ; Rocio Gallego-Duràn ; 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 ; VCTE-Prognosis Study Group
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.