Comparison of the Risk of Psychological and Cognitive Disorders Between Persistent and Nonpersistent Statin Users

被引:25
作者
Lilly, Steven M. [1 ,2 ]
Mortensen, Eric M. [1 ,2 ]
Frei, Christopher R. [3 ,4 ]
Pugh, Mary Jo [5 ,6 ]
Mansi, Ishak A. [1 ,2 ]
机构
[1] Vet Affairs North Texas Hlth Care Syst, Dept Internal Med, Dallas, TX 75216 USA
[2] Univ Texas SW Med Ctr Dallas, Dallas, TX 75390 USA
[3] Univ Texas Austin, Coll Pharm, Austin, TX 78712 USA
[4] Univ Texas Hlth Sci Ctr San Antonio, Sch Med, Pharmacotherapy Educ & Res Ctr, San Antonio, TX 78229 USA
[5] Vet Affairs South Texas Hlth Care Syst, Dept Epidemiol & Biostat, San Antonio, TX USA
[6] Univ Texas Hlth Sci Ctr San Antonio, San Antonio, TX 78229 USA
基金
美国国家卫生研究院;
关键词
TRIAL;
D O I
10.1016/j.amjcard.2014.07.010
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Despite their cardiovascular benefits, statin use has been associated with a wide array of actual or perceived psychological and cognitive adverse events. The objective of this study was to compare baseline characteristics and the risk of developing psychological and cognitive disorders between persistent and nonpersistent statin users. We performed a retrospective cohort study (October 1, 2003, to March 1, 2010) of 13,626 statin users in a regional US military health-care system. The persistence of statin use was defined by cumulative pharmacy fill data. Outcomes were the occurrence of psychological diseases during follow-up using prespecified groups based on International Classification of Diseases, Ninth Revision, codes: (1) schizophrenia and psychosis, (2) major depression and bipolar disorders, (3) all psychological diseases, and (4) dementia and cognitive disorders. Statin users who were nonpersistent at 2 years were younger, less likely to be men, and had fewer co-morbidities than persistent users. They were also more likely to be diagnosed with schizophrenia or psychosis (odds ratio [OR] 1.58, 95% confidence interval [CI] 1.20 to 2.10) and cognitive disorders (OR 1.56, 95% CI 1.19 to 2.03) during follow-up compared with persistent users. There was not an association between nonpersistence at 2 years and the development of depression and bipolar disorders (OR 0.99,95% CI 0.85 to 1.15) or combined psychological diseases (OR 0.97, 95% CI 0.86 to 1.09). Cumulative persistence with statin therapy as a continuous measure was associated with less risk of all outcomes. In conclusion, persistent statin users did not demonstrate an increase in the diagnosis of psychological disorders compared with nonpersistent users. Nonpersistent statin use was associated with a greater likelihood of being diagnosed with psychotic or cognitive disorders. Published by Elsevier Inc.
引用
收藏
页码:1035 / 1039
页数:5
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