Use of selective serotonin reuptake inhibitors and the risk of breast cancer

被引:43
作者
Coogan, PF
Palmer, JR
Strom, BL
Rosenberg, L
机构
[1] Boston Univ, Slone Epidemiol Ctr, Boston, MA 02215 USA
[2] Univ Penn, Sch Med, Dept Med, Div Gen Internal Med, Philadelphia, PA 19104 USA
[3] Univ Penn, Sch Med, Ctr Clin Epidemiol & Biostat, Dept Biostat & Epidemiol, Philadelphia, PA 19104 USA
[4] Univ Penn, Sch Med, Ctr Educ Res Therapeut, Philadelphia, PA 19104 USA
关键词
antidepressive agents; breast neoplasms; case-control studies; pharmacoepidemiology;
D O I
10.1093/aje/kwi301
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Selective serotonin reuptake inhibitors (SSRIs) were introduced in 1987 and, by 1997, were prescribed to 58% of Americans receiving outpatient treatment for depression. In 1992, a study reported that one of the SSRIs, fluoxetine, accelerated the growth of mammary tumors in rodents. By use of data from 1988 to 2002 from their hospital-based, case-control surveillance study, the authors examined the relation between use of SSRIs and risk of breast cancer. Nurse interviewers administered standard questionnaires to patients admitted to hospitals in three US centers to obtain information on demographic, medical, and lifestyle factors and to elicit a history of drug use, including antidepressants. Cases comprised 2,138 women with primary invasive breast cancer, and controls comprised 2,858 women admitted with nonmalignant diagnoses unrelated to SSRI use. The authors used multivariate conditional logistic regression models to estimate odds ratios for breast cancer among regular users of SSRIs compared with nonusers. The odds ratio was 1.1 (95% confidence interval: 0.8, 1.7) for regular use of SSRIs and 0.7 (95% confidence interval: 0.4, 1.5) for use of 4 or more years. Odds ratios were not elevated for any specific SSRI. These data provide some assurance that the use of SSRIs does not increase the risk of breast cancer.
引用
收藏
页码:835 / 838
页数:4
相关论文
共 13 条
[1]   Use of antidepressant medications and the possible association with breast cancer risk [J].
Bahl, S ;
Cotterchio, M ;
Kreiger, N .
PSYCHOTHERAPY AND PSYCHOSOMATICS, 2003, 72 (04) :185-194
[2]  
BRANDES LJ, 1992, CANCER RES, V52, P3796
[3]   EVIDENCE THAT THE ANTIESTROGEN BINDING-SITE IS A HISTAMINE OR HISTAMINE-LIKE RECEPTOR [J].
BRANDES, LJ ;
MACDONALD, LM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1985, 126 (02) :905-910
[4]   STIMULATION OF INVIVO TUMOR-GROWTH AND PHORBOL ESTER-INDUCED INFLAMMATION BY N,N-DIETHYL-2-[4-(PHENYLMETHYL)PHENOXY] ETHANAMINE HCL, A POTENT LIGAND FOR INTRACELLULAR HISTAMINE-RECEPTORS [J].
BRANDES, LJ ;
BEECROFT, WA ;
HOGG, GR .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 179 (03) :1297-1304
[5]   Comparison of self reported and physician reported antidepressant medication use [J].
Cotterchio, M ;
Kreiger, N ;
Darlington, G ;
Steingart, A .
ANNALS OF EPIDEMIOLOGY, 1999, 9 (05) :283-289
[6]  
COTTERCHIO M, 2003, AM J EPIDEMIOL, V152, P951
[7]   Breast cancer risk among users of antidepressant medications [J].
González-Pérez, A ;
Rodríguez, LAG .
EPIDEMIOLOGY, 2005, 16 (01) :101-105
[8]  
Kelly JP, 1999, AM J EPIDEMIOL, V150, P861
[9]  
Moorman PG, 2003, EPIDEMIOLOGY, V14, P307, DOI 10.1097/00001648-200305000-00010
[10]   National trends in the outpatient treatment of depression [J].
Olfson, M ;
Marcus, SC ;
Druss, B ;
Elinson, L ;
Tanielian, T ;
Pincus, HA .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2002, 287 (02) :203-209