Suppr超能文献

丙型肝炎患者中他汀类药物肝毒性的发生率。

Incidence of statin hepatotoxicity in patients with hepatitis C.

作者信息

Khorashadi Shirin, Hasson Noelle K, Cheung Ramsey C

机构信息

Pharmacy Service, VA Palo Alto Health Care System, Palo Alto, California 94304, USA.

出版信息

Clin Gastroenterol Hepatol. 2006 Jul;4(7):902-7; quiz 806. doi: 10.1016/j.cgh.2006.03.014. Epub 2006 May 11.

Abstract

BACKGROUND AND AIMS

Statins are considered contraindicated in patients with chronic liver disease. Our objective was to determine the risk of developing hepatotoxicity from statin therapy in hyperlipidemic patients with hepatitis C.

METHODS

Changes in liver biochemistry values within 12 months compared with baseline were determined in 3 cohorts matched for age, sex, and body mass index: (I) 166 anti-hepatitis C virus (HCV)-positive hyperlipidemic veterans who were initiated on statin therapy; (II) 332 anti-HCV-positive veterans who had not received statin therapy; and (III) 332 anti-HCV-negative hyperlipidemic veterans who were initiated on statin therapy. An increase in liver biochemistry values was defined as mild-moderate or severe as proposed in a previous study on statin hepatotoxicity in a non-hepatitis C population.

RESULTS

In patients with hepatitis C, statin therapy (cohort I) was associated with a higher incidence of mild-moderate liver biochemistry value increases compared with those not on statin therapy (cohort II) (22.9% vs 13.3%, respectively, P = .009), but a lower incidence of severe increases (1.2% vs 6.6%, respectively, P = .015). Among patients started on statin therapy (cohorts I and III), the incidence of mild-moderate liver biochemistry value increases (22.9% vs 16.3%, respectively, P = .094), severe increases (1.2% vs 1%, respectively, P = .874), or discontinuation of statin therapy as a result of hepatotoxicity (21.6% vs 9.2%, respectively, P = .147) were similar in hepatitis C-positive and hepatitis C-negative patients.

CONCLUSIONS

Statin therapy was not associated with a higher risk of severe hepatotoxicity in patients with chronic hepatitis C and appeared safe.

摘要

背景与目的

他汀类药物被认为对慢性肝病患者禁忌使用。我们的目的是确定丙型肝炎高脂血症患者接受他汀类药物治疗发生肝毒性的风险。

方法

在年龄、性别和体重指数匹配的3组人群中,确定与基线相比12个月内肝脏生化指标的变化:(I)166例开始接受他汀类药物治疗的抗丙型肝炎病毒(HCV)阳性高脂血症退伍军人;(II)332例未接受他汀类药物治疗的抗HCV阳性退伍军人;(III)332例开始接受他汀类药物治疗的抗HCV阴性高脂血症退伍军人。肝脏生化指标升高按照先前一项关于非丙型肝炎人群他汀类药物肝毒性的研究中所提议的标准,分为轻度 - 中度或重度。

结果

在丙型肝炎患者中,与未接受他汀类药物治疗的患者(第II组)相比,他汀类药物治疗(第I组)与轻度 - 中度肝脏生化指标升高的发生率更高相关(分别为22.9%对13.3%,P = 0.009),但重度升高的发生率较低(分别为1.2%对6.6%,P = 0.015)。在开始接受他汀类药物治疗的患者(第I组和第III组)中,丙型肝炎阳性和丙型肝炎阴性患者的轻度 - 中度肝脏生化指标升高的发生率(分别为22.9%对16.3%,P = 0.094)、重度升高的发生率(分别为1.2%对1%,P = 0.874)或因肝毒性而停用他汀类药物的发生率(分别为21.6%对9.2%,P = 0.147)相似。

结论

他汀类药物治疗与慢性丙型肝炎患者发生严重肝毒性的较高风险无关,且似乎是安全的。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验