Use of selective serotonin reuptake inhibitors and risk of developing first-time acute myocardial infarction

Citation
Cr. Meier et al., Use of selective serotonin reuptake inhibitors and risk of developing first-time acute myocardial infarction, BR J CL PH, 52(2), 2001, pp. 179-184
Citations number
42
Categorie Soggetti
Pharmacology,"Pharmacology & Toxicology
Journal title
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY
ISSN journal
03065251 → ACNP
Volume
52
Issue
2
Year of publication
2001
Pages
179 - 184
Database
ISI
SICI code
0306-5251(200108)52:2<179:UOSSRI>2.0.ZU;2-1
Abstract
Aims Selective serotonin reuptake inhibitors (SSRIs) have been associated w ith serotonin depletion in platelets, potentially leading to abnormal aggre gation and prolonged bleeding time. In view of the importance of serotonin in coronary thrombosis, and decreased platelet serotonin concentrations ass ociated with SSRIs, the present study was performed to test the hypothesis of a decreased risk of acute myocardial infarction (AMI) associated with SS RIs. Methods We conducted a population-based case-control analysis using the UK General Practice Research Database (GPRD). A total of 3319 patients aged 75 years or younger free of clinical conditions predisposing to ischaemic hea rt disease, with a first-time diagnosis of AMI between 1992 and 1997, and 1 3 139 controls without AMI matched to cases for age, sex, general practice attended, and calendar time were included. Conditional logistic regression was used to estimate relative risks. Results Adjusted odds ratios (with 95% CI) for current use of SSRIs, non-SS RIs, or other antidepressants, compared to the group of nonusers of antidep ressants were 0.9 (95% CI 0.5,1.8), 0.9 (95% CI 0.7,1.2), and 1.3 (95% CI 0 .6,2.8), respectively. As compared with nonuse of SSRIs, current use (regar dless of any other antidepressants used) resulted in an adjusted OR of 1.1 (95% CI 0.7,1.6). Conclusions The current analysis provides evidence that SSRI exposure does not substantially decrease the risk of developing first-time AMI in patient s free of factors predisposing to ischaemic heart disease. However, due to relatively small numbers of exposed subjects and the resulting wide confide nce intervals, further studies may be needed to document a lack of effect o f SSRIs in subjects without pre-existing diseases predisposing to AMI.