Long-term Statin Use and the Risk of Gallstone Disease: A Population-based Case-Control Study

被引:53
作者
Erichsen, Rune [1 ]
Froslev, Trine [1 ]
Lash, Timothy L. [1 ,2 ]
Pedersen, Lars [1 ]
Sorensen, Henrik Toft [1 ,2 ]
机构
[1] Aarhus Univ Hosp, Dept Clin Epidemiol, DK-8200 Aarhus N, Denmark
[2] Boston Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA USA
关键词
cholelithiasis; gallstones; hydroxymethylglutaryl-CoA reductase inhibitors; risk; HMG-COA REDUCTASE; CHOLESTEROL; SIMVASTATIN; INHIBITOR; BILE; CHOLECYSTECTOMY; PRAVASTATIN; PREVALENCE; METABOLISM; COHORT;
D O I
10.1093/aje/kwq361
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Most gallstones originate from cholesterol-supersaturated bile. Statins inhibit hepatic cholesterol biosynthesis and therefore may reduce the risk of gallstone disease. Population-based evidence, however, is sparse. Thus, the authors conducted a population-based case-control study using medical databases from northern Denmark (1.7 million inhabitants) to identify 32,494 cases of gallstones occurring between 1996 and 2008 and to identify age-, sex-, and county-matched population controls for each case. Cases and their matched controls who were exposed to lipid-lowering drugs were categorized as current users if their last prescription was redeemed < 90 days before the case's diagnosis date; otherwise, they were categorized as former users. Conditional logistic regression was used to estimate adjusted odds ratios and 95% confidence intervals for gallstone disease in patients treated with lipid-lowering drugs. In current users, the adjusted odds ratios associating statin use with the occurrence of gallstone disease were 1.17 (95% confidence interval (CI): 1.06, 1.30) for those who had 1-4 prescriptions, 0.89 (95% CI: 0.80, 0.97) for those who had 5-19 prescriptions, and 0.76 (95% CI: 0.69, 0.84) for those who had >= 20 total prescriptions. In former users, the corresponding adjusted odds ratios were 1.24 (95% CI: 1.11, 1.39), 0.97 (95% CI: 0.86, 1.10), and 0.79 (95% CI: 0.64, 0.97), respectively. The use of other lipid-lowering drugs showed no similar association.
引用
收藏
页码:162 / 170
页数:9
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