Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan; Geriatric Mental Health Program, Centre for Addiction and Mental Health, Toronto, ON, Canada.
J Affect Disord. 2013 Nov;151(2):506-513. doi: 10.1016/j.jad.2013.06.035. Epub 2013 Jul 22.
It remains unclear regarding the contribution of each individual symptom in predicting the outcome in major depressive disorder (MDD). The objective of this analysis was to evaluate trajectories of individual symptoms over time to identify which specific depressive item(s) could predict subsequent clinical response.
The data of 2874 outpatients with nonpsychotic MDD who received citalopram for up to 14 weeks in the Sequenced Treatment Alternatives to Relieve Depression (STAR*D) trial were analyzed. Average trajectories of individual symptoms over time were estimated for remitters and non-remitters. Moreover, specific symptoms whose improvement at week 2 predicted remission were identified, using binary logistic regression analysis.
Trajectories were significantly different between remitters and non-remitters in all depressive symptoms. All depressive symptoms in the 16-item Quick Inventory of Depressive Symptomatology, Self-Report (QIDS-SR16) in the two groups, except for hypersomnia and weight change in non-remitters, substantially improved within 2 weeks and gradually continued to improve thereafter throughout the 14 weeks. Early improvements in the following five symptoms, in order of magnitude, in the QIDS-SR16 were significantly associated with remission: sad mood, negative self-view, feeling slowed down, low energy, and restlessness (P<0.001, P<0.001, P=0.001, P=0.004, P=0.021).
The participants were limited to the nonpsychotic MDD outpatients who received citalopram. Further, symptomatology was not evaluated at the very beginning of treatment.
While the data pertain to citalopram and replication is necessary for other antidepressants, early improvements in certain core depressive symptoms may serve as a predictor of subsequent remission.
目前尚不清楚在预测重度抑郁症(MDD)结局方面,个体症状的贡献如何。本分析旨在评估个体症状随时间的轨迹,以确定哪些特定的抑郁项目可以预测随后的临床反应。
对接受西酞普兰治疗长达 14 周的 2874 例非精神病性 MDD 门诊患者的 Sequenced Treatment Alternatives to Relieve Depression(STAR*D)试验数据进行了分析。估计了缓解者和非缓解者随时间推移的个体症状的平均轨迹。此外,使用二项逻辑回归分析,确定了第 2 周改善可预测缓解的特定症状。
缓解者和非缓解者的所有抑郁症状的轨迹均存在显著差异。两组人群中除非缓解者的嗜睡和体重变化外,16 项简明抑郁症状自评量表(QIDS-SR16)中的所有抑郁症状在 2 周内显著改善,并在随后的 14 周内逐渐改善。QIDS-SR16 中以下五个症状在早期改善的幅度,按顺序与缓解显著相关:悲伤情绪、消极的自我看法、动作缓慢、精力不足和烦躁不安(P<0.001,P<0.001,P=0.001,P=0.004,P=0.021)。
参与者仅限于接受西酞普兰治疗的非精神病性 MDD 门诊患者。此外,治疗开始时并未评估症状。
虽然这些数据适用于西酞普兰,且需要其他抗抑郁药的验证,但某些核心抑郁症状的早期改善可能是随后缓解的预测指标。