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
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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.</p><p><strong>Results: </strong>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). 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引用次数: 0
摘要
背景:目的:探讨他汀类药物对代谢相关性脂肪性肝病(MASLD)患者全因死亡、肝脏相关临床事件(LREs)和肝脏僵化进展的长期风险的影响:这项队列研究收集了在16家三级转诊中心接受至少两次振动控制瞬态弹性成像检查的MASLD患者的数据。通过Cox回归分析,研究了他汀类药物的使用与全因死亡和LREs长期风险之间的关系,并按代偿性晚期慢性肝病(cACLD)进行了分层:基线肝硬度测量值(LSM)≥10 kPa。肝硬度进展的定义是:cACLD 和 LRE 的肝硬度测量值增加≥20%:我们对基线 LSM 为 5.9 kPa(IQR 4.6-8.2)的 7988 名患者进行了中位 4.6 年的随访。基线时,40.5% 的患者使用他汀类药物,17% 的患者存在 cACLD。使用他汀类药物与较低的全因死亡风险(调整后HR=0.233;95% CI 0.127至0.426)和LRE风险(调整后HR=0.380;95% CI 0.268至0.539)明显相关。使用他汀类药物还与cACLD(HR=0.542;95% CI 0.389至0.755)和非cACLD(调整后HR=0.450;95% CI 0.342至0.592)肝硬变进展率降低有关,但与肝硬变回归无关(调整后HR=0.914;95% CI 0.778至1.074):使用他汀类药物与MASLD患者相对较低的全因死亡率、LRE和肝硬变进展的长期风险相关。
Long-term liver-related outcomes and liver stiffness progression of statin usage in steatotic liver disease.
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.
期刊介绍:
Gut is a renowned international journal specializing in gastroenterology and hepatology, known for its high-quality clinical research covering the alimentary tract, liver, biliary tree, and pancreas. It offers authoritative and current coverage across all aspects of gastroenterology and hepatology, featuring articles on emerging disease mechanisms and innovative diagnostic and therapeutic approaches authored by leading experts.
As the flagship journal of BMJ's gastroenterology portfolio, Gut is accompanied by two companion journals: Frontline Gastroenterology, focusing on education and practice-oriented papers, and BMJ Open Gastroenterology for open access original research.