Beneficial Effects of Statins on the Rates of Hepatic Fibrosis, Hepatic Decompensation, and Mortality in Chronic Liver Disease: A Systematic Review and Meta-Analysis

被引:80
|
作者
Kamal, Sehrish [1 ]
Khan, Muhammad Ali [1 ]
Seth, Ankur [1 ]
Cholankeril, George [1 ]
Gupta, Deepansh [1 ]
Singh, Utkarsh [1 ]
Kamal, Faisal [1 ]
Howden, Colin W. [1 ]
Stave, Christopher [2 ]
Nair, Satheesh [1 ]
Satapathy, Sanjaya K. [1 ]
Ahmed, Aijaz [3 ]
机构
[1] Univ Tennessee, Ctr Hlth Sci, Div Gastroenterol & Hepatol, Memphis, TN 38163 USA
[2] Stanford Univ, Lane Med Lib, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Div Gastroenterol & Hepatol, 750 Welch Rd,210 Palo Alto, Stanford, CA 94304 USA
来源
AMERICAN JOURNAL OF GASTROENTEROLOGY | 2017年 / 112卷 / 10期
关键词
TISSUE GROWTH-FACTOR; HEPATOCELLULAR-CARCINOMA; CIRRHOSIS; RISK; SIMVASTATIN; THERAPY; ATORVASTATIN; INHIBITION; SURVIVAL; QUALITY;
D O I
10.1038/ajg.2017.170
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
OBJECTIVES: Statins may improve outcomes in patients with chronic liver disease (CLD). We conducted a systematic review and meta-analysis to evaluate the impact of statins in the setting of CLD. METHODS: We searched several databases from inception to 17 October 2016 to identify comparative studies evaluating the role of statins in CLD. Outcomes of interest were the associations between statin use and progression of fibrosis, development of hepatic decompensation in cirrhosis, and mortality in CLD. Adjusted hazard ratios (HRs) were pooled and analyzed using a random effects model. Subgroup analyses were performed based on the method of detection for progression of hepatic fibrosis and quality of studies. RESULTS: We included 10 studies (1 randomized controlled trial and 9 observational) with 259,453 patients (54,441 statin users and 205,012 nonusers). For progression of hepatic fibrosis, pooled HR (95% confidence interval) was 0.49 (0.39-0.62). On subgroup analysis of studies using ICD-9 (The International Classification of Diseases, Ninth Revision) coding and a second method to detect cirrhosis, pooled HR was 0.58 (0.51-0.65); pooled HR for studies using ICD-9 coding only was 0.36 (0.29-0.44). For progression of fi brosis in patients with hepatitis C virus (HCV) infection, pooled HR was 0.52 (0.37-0.73). For hepatic decompensation in cirrhosis, pooled HR was 0.54 (0.46-0.65). For mortality, pooled HR based on observational studies was 0.67 (0.46-0.98); in the randomized controlled trial, HR was 0.39 (0.15-0.99). However, the quality of evidence for these associations is low as most included studies were retrospective in nature and limited by residual confounding. CONCLUSIONS: Statins may retard the progression of hepatic fi brosis, may prevent hepatic decompensation in cirrhosis, and may reduce all-cause mortality in patients with CLD. As the quality (certainty) of evidence is low, further studies are needed before statins can be routinely recommended.
引用
收藏
页码:1495 / 1505
页数:11
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