MRC Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, King's College London, United Kingdom.
J Affect Disord. 2011 Jul;132(1-2):112-20. doi: 10.1016/j.jad.2011.02.014. Epub 2011 Mar 15.
To investigate whether subtypes of depression predict differential outcomes of treatment with selective serotonin-reuptake inhibitor (SSRI) and a tricyclic antidepressant in major depression.
Among 811 adults with moderate-to-severe depression, melancholic, atypical, anxious and anxious-somatizing depression subtypes established at baseline were evaluated as predictors of outcome of treatment with flexible dosage of the SSRI escitalopram or the tricyclic antidepressant nortriptyline. The primary outcome measure was the Montgomery-Åsberg Depression Rating Scale (MADRS). Secondary outcome measures were the 17-item Hamilton Rating Scale for Depression (HRSD-17) and the Beck Depression Inventory (BDI).
Melancholic depression was associated with slightly worse outcomes among individuals treated with escitalopram, but did not affect outcome of treatment with nortriptyline. The interaction between melancholic depression and drug did not reach statistical significance for the primary outcome measure and significant results for secondary outcome measures were not robust in sensitivity analyses. Atypical depression was unrelated to outcome of treatment with either antidepressant. Anxious and anxious-somatizing depression did not predict outcome on the primary measure, but inconsistently predicted worse outcome in some secondary analyses.
Some participants were non-randomly allocated to drug. Therefore, drug-by-predictor interactions had to be validated in sensitivity analyses restricted to the 468 randomly allocated individuals.
Melancholic, atypical or anxious depression, are not sufficiently robust differential predictors of outcome to help clinician choose between SSRI and tricyclic antidepressants. There is a need to investigate other predictors of outcome.
探讨抑郁症亚型是否可以预测选择性 5-羟色胺再摄取抑制剂(SSRI)和三环类抗抑郁药治疗重度抑郁症的不同结局。
在 811 名中重度抑郁症患者中,根据基线时确定的忧郁型、非典型型、焦虑型和焦虑躯体化型抑郁亚型,评估其对 SSRI 依地普仑或三环类抗抑郁药去甲替林灵活剂量治疗结局的预测作用。主要结局指标为蒙哥马利-阿斯伯格抑郁评定量表(MADRS)。次要结局指标为汉密尔顿抑郁评定量表(HRSD-17)和贝克抑郁量表(BDI)。
忧郁型抑郁症与依地普仑治疗个体的结局略差相关,但不影响去甲替林的治疗结局。忧郁型抑郁症与药物之间的相互作用对主要结局指标没有达到统计学意义,而对次要结局指标的显著结果在敏感性分析中并不稳健。非典型型抑郁症与两种抗抑郁药的治疗结果无关。焦虑型和焦虑躯体化型抑郁症不能预测主要指标的治疗结果,但在一些次要分析中不一致地预测预后较差。
部分参与者未随机分配药物。因此,必须在仅对 468 名随机分配个体进行的敏感性分析中验证药物-预测因子相互作用。
忧郁型、非典型型或焦虑型抑郁症作为预后的预测因子并不稳健,无法帮助临床医生在 SSRI 和三环类抗抑郁药之间进行选择。需要进一步研究其他预后预测因子。