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GRAZIA PENNISI

Long-term liver-related outcomes and liver stiffness progression of statin usage in steatotic liver disease

  • Autori: Zhou X.-D.; Kim S.U.; Yip T.C.-F.; Petta S.; Nakajima A.; Tsochatzis E.; Boursier J.; Bugianesi E.; Hagstrom H.; Chan W.K.; Romero-Gomez M.; Calleja J.L.; de Ledinghen V.; Castera L.; Sanyal A.J.; Goh G.B.-B.; Newsome P.N.; Fan J.; Lai M.; Fournier-Poizat C.; Lee H.W.; Wong G.L.-H.; Armandi A.; Shang Y.; Pennisi G.; Llop E.; Yoneda M.; de Saint-Loup M.; Canivet C.M.; Lara-Romero C.; Gallego-Duran R.; Asgharpour A.; Teh K.K.-J.; Mahgoub S.; Chan M.S.-W.; Lin H.; Liu W.-Y.; Targher G.; Byrne C.D.; Wong V.W.-S.; Zheng M.-H.
  • Anno di pubblicazione: 2024
  • Tipologia: Articolo in rivista
  • OA Link: http://hdl.handle.net/10447/659258

Abstract

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.