Wang Li Yueh, Huang Yi-Shin, Perng Chin-Lin, Huang Bryan, Lin Han-Chieh
Division of Gastroenterology and Hepatology, Department of Medicine, Taipei Veterans General Hospital and National Yang-Ming University School of Medicine, Taipei, Taiwan.
Division of Gastroenterology, Department of Medicine, Cardinal Tien Hospital, New Taipei City, Taiwan.
Br J Clin Pharmacol. 2016 Sep;82(3):823-30. doi: 10.1111/bcp.13009. Epub 2016 Jun 17.
Statin-induced liver injury (SILI) is quite rare, but may be severe. Little is known about the impact of chronic hepatitis B infection (CHBI) on SILI. We aimed to investigate the risk factors and outcome of SILI, with special reference to its interaction with CHBI.
Patients with SILI were recruited from our hospital, and three-to-one drug-matched controls were randomly selected. The clinical data of the patients were then compared.
A total of 108 patients with SILI and 324 controls were enrolled. The patients with SILI were both older and had a higher statin dose than the controls. There was no predilection of liver injury associated with the seven available statins. Among the SILI patients, there was no statistical difference between the baseline and peak liver enzyme tests, and latency and severity between hepatitis B carriers (n = 16) and non-carriers (n = 92). High dose of statin and age were the two independent risk factors of SILI (OR and 95% CI: 1.93, 1.08-3.35, P = 0.025, and 1.73, 1.07-2.80, P = 0.027, respectively). Permanent discontinuation of statin was noted in 50 (46.3%) patients with SILI due to severe SILI or recurrent hepatotoxicity after rechallenge of other statins.
High dose of statin and old age may increase patient susceptibility to SILI; however, CHBI and abnormal baseline liver tests are not risk factors of SILI. Nonetheless, SILI is still worthy of notice, because nearly half of the overt cases discontinued statin treatment due to severe hepatotoxicity in this study.
他汀类药物所致肝损伤(SILI)相当罕见,但可能很严重。关于慢性乙型肝炎感染(CHBI)对SILI的影响知之甚少。我们旨在研究SILI的危险因素和结局,特别关注其与CHBI的相互作用。
从我院招募SILI患者,并随机选择三比一的药物匹配对照。然后比较患者临床资料。
共纳入108例SILI患者和324例对照。SILI患者年龄更大且他汀类药物剂量高于对照。七种可用他汀类药物所致肝损伤无偏好性差异。在SILI患者中,乙肝携带者(n = 16)与非携带者(n = 92)之间的基线和峰值肝酶检测、潜伏期和严重程度无统计学差异。高剂量他汀类药物和年龄是SILI的两个独立危险因素(OR及95%CI分别为:1.93,1.08 - 3.35,P = 0.025;1.73,1.07 - 2.80,P = 0.027)。50例(46.3%)SILI患者因严重SILI或再次使用其他他汀类药物后复发性肝毒性而永久停用他汀类药物。
高剂量他汀类药物和高龄可能增加患者对SILI的易感性;然而,CHBI和基线肝检测异常不是SILI的危险因素。尽管如此,SILI仍值得关注,因为在本研究中近一半的显性病例因严重肝毒性而停用他汀类药物治疗。