Risk of ovarian cancer according to use of antidepressants, phenothiazines, and benzodiazepines (United States)

Citation
Pf. Coogan et al., Risk of ovarian cancer according to use of antidepressants, phenothiazines, and benzodiazepines (United States), CANC CAUSE, 11(9), 2000, pp. 839-845
Citations number
14
Categorie Soggetti
Envirnomentale Medicine & Public Health
Journal title
CANCER CAUSES & CONTROL
ISSN journal
09575243 → ACNP
Volume
11
Issue
9
Year of publication
2000
Pages
839 - 845
Database
ISI
SICI code
0957-5243(200011)11:9<839:ROOCAT>2.0.ZU;2-C
Abstract
Objectives: An association of increased risk of ovarian cancer with use of antidepressants or benzodiazepine tranquilizers has been reported from a ca se-control study. We assessed the association between ovarian cancer risk a nd the use of tricyclic antidepressants, selective serotonin reuptake inhib itors (SSRIs), phenothiazine antipsychotics, and benzodiazepines, in data f rom the Case-Control Surveillance Study. Methods: From 1976 through 1998, data were collected from hospital patients in Boston, New York, Philadelphia, and Baltimore based on demographic fact ors, reproductive and medical history, and medication use. In the present a nalyses, cases of epithelial ovarian cancer (n = 748) were compared with ca ncer controls (n = 1496) and noncancer controls admitted for trauma and acu te infection (n = 1496). We estimated Mantel-Haenszel odds ratios adjusted for age, study center, and year of interview. Results: Odds ratios for regular use (at least 4 days/week for at least 1 m onth) were compatible with 1.0 for every drug class. For tricyclics and ben zodiazepines the upper 95% confidence limits were less than 1.6. For phenot hiazines the upper limit was 2.6 with cancer controls and 1.4 with noncance r controls. Only five cases used SSRIs, yielding unstable results. Odds rat ios were not increased among women who had used any drug class for at least 5 years, nor among women who had first used them 10 or more years previous ly. Conclusions: These data do not support an association between regular use o f any of the drugs under study with ovarian cancer risk.