Statin use and risk of basal cell carcinoma

被引:12
作者
Asgari, Maryam A. [1 ,2 ]
Tang, Jean [2 ,5 ]
Epstein, Ervin H., Jr. [5 ]
Chren, Mary-Margaret [2 ,4 ]
Warton, E. Margaret [1 ]
Quesenberry, Charles P., Jr. [1 ]
Go, Alan S. [1 ,3 ]
Friedman, Gary D. [1 ,6 ]
机构
[1] Kaiser Permanente No Calif, Div Res, Oakland, CA 94612 USA
[2] Univ Calif San Francisco, Dept Dermatol, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Biostat Epidemiol & Med, San Francisco, CA 94143 USA
[4] San Francisco VA Med Ctr, Hlth Serv Res Enhancement Award Program, San Francisco, CA USA
[5] Childrens Hosp, Oakland Res Inst, Oakland, CA USA
[6] Stanford Univ, Sch Med, Dept Hlth Res & Policy, Stanford, CA 94305 USA
关键词
basal cell carcinoma; pharmacoepidemiology; skin cancer; statin; NONMELANOMA SKIN-CANCER; FOLLOW-UP; METAANALYSIS; SIMVASTATIN; PREVENTION; LOVASTATIN; REGRESSION; EZETIMIBE;
D O I
10.1016/j.jaad.2009.02.011
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Objective: We examined the association between statin use and basal cell carcinoma (BCC) risk. Methods: We identified all members of a large integrated health care delivery system with a diagnosis of a histologically proven BCC in 1997. Subsequent BCCs were identified through 2006 from health plan electronic pathology records. Longitudinal exposure to statins and other lipid-lowering agents was determined from automated pharmacy records. We used extended Cox regression to examine the independent association between receipt of statin therapy (ever vs never, cumulative duration) and risk of subsequent BCC. To minimize confounding by indication, we conducted sensitivity analyses in the subset of individuals considered eligible for lipid-lowering therapy based on national guidelines. Results: Among 12,123 members given a diagnosis of BCC who had no prior statin exposure, 6381 developed a subsequent BCC during follow-up. Neither "ever use of statins" (adjusted hazard ratio 1.02, 95% confidence interval: 0.92-1.12) or Cumulative duration of statin (adjusted hazard ratio 1.02/year, 95% confidence interval: 0.99-1.11) was associated With subsequent BCC after adjustment for age, sex, and health care use. Risk estimates did not change appreciably when the analysis was limited to the Subset of individuals who met eligibility criteria for initiating statin therapy. There was also no significant association between use of non-statin antilipemics and subsequent BCC (adjusted hazard ratio 1.10, 95% confidence interval: 0.76-1-58). Limitations: No information was available for BCC risk factors, Such as sun sensitivity and sun exposure. Conclusions: Among a large cohort of individuals with BCC, statin therapy was not significantly associated with risk of subsequent BCC. (J Am Acad Dermatol 2009;61:66-72.)
引用
收藏
页码:66 / 72
页数:7
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