Lund University, Faculty of Medicine, Department of Clinical Sciences, Psychiatry, Lund, Sweden.
Department of Psychiatry, University of California San Francisco (UCSF) School of Medicine, San Francisco, CA, USA.
J Affect Disord. 2019 May 1;250:65-70. doi: 10.1016/j.jad.2019.02.063. Epub 2019 Feb 26.
BACKGROUND: Less than half of patients with major depressive disorder (MDD) respond to their first antidepressant trial. Our understanding of the underlying mechanisms of selective serotonin reuptake inhibitors (SSRIs) remains poor, and there is no reliable method of predicting treatment response. METHODS: Thirty-seven MDD subjects and 41 healthy controls, somatically healthy and medication-free for at least six weeks, were recruited, and plasma serotonin (5-HT) levels were assessed at baseline. Twenty-six of the MDD subjects were then treated in an open-label manner with clinically appropriate doses of sertraline for 8 weeks, after which plasma 5-HT levels were again assessed. Response to treatment was defined as an improvement of 50% or more on the Hamilton Depression Rating Scale. RESULTS: Non-responders to sertraline treatment had significantly lower pre-treatment 5-HT levels compared to both healthy controls and responders (F = 4.4, p = 0.004 and p = 0.036, respectively). There was a significant decrease in 5-HT levels over treatment in all MDD subjects (t = 6.2, p = 0.000003). The decrease was significantly more prominent in responders compared to non-responders (t = 2.1, p = 0.047). There was no significant difference in post-treatment 5-HT levels between responders and non-responders. LIMITATIONS: The study had a modest sample size. 5-HT levels in plasma may not reflect 5-HT levels in the brain. CONCLUSIONS: The results indicate that SSRI response may be facilitated by adequate baseline plasma 5-HT content and that successful SSRI treatment is associated with greater decreases in circulating 5-HT. Plasma 5-HT content may be a predictor of SSRI treatment outcome. Potential underlying mechanisms are discussed.
背景:不足半数的重度抑郁症(MDD)患者对其首次抗抑郁药物治疗有反应。我们对选择性 5-羟色胺再摄取抑制剂(SSRIs)的潜在机制的了解仍然有限,而且目前还没有可靠的方法来预测治疗反应。
方法:招募了 37 名 MDD 患者和 41 名健康对照者,他们身体健康,且至少六周内未服用任何药物。在基线时评估了他们的血浆 5-羟色胺(5-HT)水平。然后,26 名 MDD 患者以开放标签的方式接受临床适宜剂量的舍曲林治疗 8 周,之后再次评估血浆 5-HT 水平。治疗反应定义为汉密尔顿抑郁评定量表(Hamilton Depression Rating Scale)评分改善 50%或以上。
结果:舍曲林治疗无反应者的治疗前 5-HT 水平明显低于健康对照组和有反应者(F=4.4,p=0.004 和 p=0.036)。所有 MDD 患者的 5-HT 水平在治疗过程中均显著下降(t=6.2,p=0.000003)。与无反应者相比,有反应者的下降更为显著(t=2.1,p=0.047)。有反应者和无反应者之间的治疗后 5-HT 水平没有显著差异。
局限性:该研究样本量较小。血浆中的 5-HT 水平可能无法反映大脑中的 5-HT 水平。
结论:研究结果表明,SSRIs 的反应可能与基线时的血浆 5-HT 含量有关,且 SSRIs 的成功治疗与循环 5-HT 水平的显著降低有关。血浆 5-HT 含量可能是 SSRIs 治疗结果的预测指标。讨论了潜在的机制。
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