Noordam Raymond, Aarts Nikkie, Leening Maarten J G, Tiemeier Henning, Franco Oscar H, Hofman Albert, Stricker Bruno H, Visser Loes E
Department of Internal Medicine, Erasmus MC-University Medical Center Rotterdam, Rotterdam, The Netherlands.
Department of Epidemiology, Erasmus MC-University Medical Center Rotterdam, P.O. Box 2040, 3000 CA, Rotterdam, The Netherlands.
Eur J Clin Pharmacol. 2016 Feb;72(2):211-8. doi: 10.1007/s00228-015-1972-2. Epub 2015 Nov 7.
Antidepressants, specifically selective serotonin reuptake-inhibiting antidepressants (SSRIs), decrease platelet activation and aggregation in in vitro experiments and could therefore decrease the risk of myocardial infarction (MI). However, prior studies addressing this hypothesis showed contradictory results. Our purpose was to investigate the association between the use of any antidepressant drug and incident MI among middle-aged and older adults.
We embedded a case-control study in the prospective Rotterdam Study (1991-2011). Controls were matched to MI cases based on sex and age at the same calendar date, and confounding factors were taken into account as time-varying covariates. The relative risk of MI during current and past use of an antidepressant was analyzed with conditional logistic regression with never use of antidepressant drugs as the reference category.
A total of 744 out of a cohort of 9499 study participants developed MI during follow-up. After statistical adjustment for traditional cardiovascular risk factors and depression, current use of any antidepressant was associated with a lower risk of MI (odds ratio (OR), 0.71; 95 % confidence interval (CI), 0.51-0.98) compared with never use of any antidepressant. SSRI use showed the lowest relative risk (OR, 0.65; 95 % CI, 0.41-1.02), albeit marginally not statistically significant. Past use of any of the antidepressant classes was not associated with a lower risk of MI.
Current use of antidepressants was associated with a lower risk of MI. Of the different classes, the use of SSRIs showed the lowest risk of MI, and therefore confirming the research hypothesis.
在体外实验中,抗抑郁药,特别是选择性5-羟色胺再摄取抑制型抗抑郁药(SSRI),可降低血小板的活性和聚集,因此可能降低心肌梗死(MI)风险。然而,此前针对这一假设的研究结果相互矛盾。我们的目的是研究在中老年人中使用任何抗抑郁药物与新发心肌梗死之间的关联。
我们在鹿特丹前瞻性研究(1991 - 2011年)中纳入了一项病例对照研究。根据相同日历日期的性别和年龄,将对照与心肌梗死病例进行匹配,并将混杂因素作为随时间变化的协变量加以考虑。以从未使用过抗抑郁药物为参照类别,采用条件逻辑回归分析当前和过去使用抗抑郁药期间发生心肌梗死的相对风险。
在9499名研究参与者的队列中,共有744人在随访期间发生心肌梗死。在对传统心血管危险因素和抑郁症进行统计学调整后,与从未使用过任何抗抑郁药相比,当前使用任何抗抑郁药与较低的心肌梗死风险相关(优势比(OR)为0.71;95%置信区间(CI)为0.51 - 0.98)。使用SSRI的相对风险最低(OR为0.65;95%CI为0.41 - 1.02),尽管在统计学上勉强不显著。过去使用任何一类抗抑郁药与较低的心肌梗死风险均无关联。
当前使用抗抑郁药与较低的心肌梗死风险相关。在不同类别中,使用SSRI的心肌梗死风险最低,从而证实了研究假设。