Long-term liver-related outcomes and liver stiffness progression of statin usage in steatotic liver disease
Author:
Zhou Xiao-DongORCID, Kim Seung UpORCID, Yip Terry Cheuk-FungORCID, Petta SalvatoreORCID, Nakajima Atsushi, Tsochatzis Emmanuel, Boursier JérômeORCID, Bugianesi ElisabettaORCID, Hagström HannesORCID, Chan Wah KheongORCID, Romero-Gomez ManuelORCID, Calleja José LuisORCID, de Lédinghen Victor, Castéra Laurent, Sanyal Arun J, Goh George Boon-Bee, Newsome Philip NORCID, Fan Jiangao, Lai Michelle, Fournier-Poizat Céline, Lee Hye WonORCID, Wong Grace Lai-HungORCID, Armandi AngeloORCID, Shang YingORCID, Pennisi GraziaORCID, Llop Elba, Yoneda Masato, Saint-Loup Marc de, Canivet Clemence MORCID, Lara-Romero Carmen, Gallego-Duràn Rocio, Asgharpour Amon, Teh Kevin Kim-Jun, Mahgoub Sara, Chan Mandy Sau-Wai, Lin Huapeng, Liu Wen-Yue, Targher GiovanniORCID, Byrne Christopher DORCID, Wong Vincent Wai-SunORCID, Zheng Ming-HuaORCID
Abstract
BackgroundStatins have multiple benefits in patients with metabolic-associated steatotic liver disease (MASLD).AimTo 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.MethodsThis 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.ResultsWe 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).ConclusionsStatin usage was associated with a relatively lower long-term risk of all-cause mortality, LREs and liver stiffness progression in patients with MASLD.
Funder
the Southampton National Institute for Health and Care Research (NIHR) Biomedical Research Centre National Key Research and Development Program of China National Natural Science Foundation of China
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