Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Department of Psychiatry, Warneford Hospital, University of Oxford, Oxford, UK.
Neuropsychopharmacology. 2023 Nov;48(12):1760-1768. doi: 10.1038/s41386-023-01676-3. Epub 2023 Jul 28.
There is concern regarding the impact of selective serotonin reuptake inhibitors (SSRIs) on suicidal behaviour. Using the target trial framework, we investigated the effect on suicidal behaviour of SSRI treatment following a depression diagnosis. We identified 162,267 individuals receiving a depression diagnosis aged 6-59 years during 2006-2018 in Stockholm County, Sweden, after at least 1 year without antidepressant dispensation. Individuals who initiated an SSRI within 28 days of the diagnosis were assigned as SSRI initiators, others as non-initiators. Intention-to-treat and per-protocol effects were estimated; for the latter, individuals were censored when they ceased adhering to their assigned treatment strategy. We applied inverse probability weighting (IPW) to account for baseline confounding in the intention-to-treat analysis, and additionally for treatment non-adherence and time-varying confounding in the per-protocol analysis. The suicidal behaviour risk difference (RD), and risk ratio (RR) between SSRI initiators and non-initiators were estimated at 12 weeks. In the overall cohort, we found an increased risk of suicidal behaviour among SSRI initiators (intention-to-treat RR = 1.50, 95% CI = 1.25, 1.80; per-protocol RR = 1.69, 95% CI = 1.20, 2.36). In age strata, we only found evidence of an increased risk among individuals under age 25, with the greatest risk among 6-17-year-olds (intention-to-treat RR = 2.90, 95% CI = 1.72, 4.91; per-protocol RR = 3.34, 95% CI = 1.59, 7.00). Our finding of an increased suicidal behaviour risk among individuals under age 25 reflects evidence from RCTs. We found no evidence of an effect in the high-risk group of individuals with past suicidal behaviour. Further studies with information on a wider array of confounders are called for.
人们担心选择性 5-羟色胺再摄取抑制剂(SSRIs)对自杀行为的影响。我们使用目标试验框架,研究了 SSRIs 治疗对抑郁症诊断后的自杀行为的影响。我们在瑞典斯德哥尔摩县确定了 162267 名年龄在 6-59 岁之间的个体,这些个体在至少 1 年未接受抗抑郁药治疗后,在 2006-2018 年期间被诊断患有抑郁症,且至少在 1 年内未接受抗抑郁药治疗。在诊断后 28 天内开始使用 SSRIs 的个体被分配为 SSRI 启动者,其他个体为非启动者。我们估计了意向治疗和按方案治疗的效果;对于后者,当个体停止遵守其分配的治疗策略时,对个体进行了删失。我们应用逆概率加权(IPW)来解释意向治疗分析中的基线混杂因素,并且在按方案治疗分析中还解释了治疗不依从性和随时间变化的混杂因素。在 12 周时,计算了 SSRI 启动者和非启动者之间自杀行为风险差异(RD)和风险比(RR)。在整个队列中,我们发现 SSRI 启动者的自杀行为风险增加(意向治疗 RR=1.50,95%CI=1.25,1.80;按方案治疗 RR=1.69,95%CI=1.20,2.36)。在年龄分层中,我们仅发现 25 岁以下个体的风险增加,其中 6-17 岁个体的风险最大(意向治疗 RR=2.90,95%CI=1.72,4.91;按方案治疗 RR=3.34,95%CI=1.59,7.00)。我们发现 25 岁以下个体自杀行为风险增加的结果反映了 RCTs 的证据。我们没有发现过去有自杀行为的高危人群有影响的证据。需要进一步研究,以获取更广泛的混杂因素信息。