Mood Disorder Psychopharmacology Unit, University Health Network, Toronto, ON, Canada; Canadian Rapid Treatment Center of Excellence, Mississauga, ON, Canada; Brain and Cognition Discovery Foundation, Toronto, ON, Canada; Department of Psychiatry, University of Toronto, Toronto, ON, Canada; Department of Pharmacology and Toxicology, University of Toronto, Toronto, ON, Canada.
Mood Disorder Psychopharmacology Unit, University Health Network, Toronto, ON, Canada; Canadian Rapid Treatment Center of Excellence, Mississauga, ON, Canada.
J Affect Disord. 2021 Sep 1;292:714-719. doi: 10.1016/j.jad.2021.05.090. Epub 2021 Jun 20.
The efficacy of monoamine-based antidepressants in adults with major depressive disorder (MDD) is attenuated in persons with greater pre-treatment functional impairment. Herein, we investigated whether pre-treatment functioning in outpatients with treatment-resistant depression (TRD) moderates response to intravenous (IV) ketamine.
Adults (N= 326; M = 45) with DSM-5-defined MDD or bipolar disorder and TRD received repeat-dose IV ketamine at a community-based clinic. Function was evaluated with the Sheehan Disability Scale (SDS), using total scores as well as scores on the subdomains of workplace/school, social life, and family life/home responsibilities. The primary dependent measure was change in depressive symptoms from pre-treatment to post-infusion 4, as measured by the Quick Inventory for Depressive Symptomatology-Self Report-16.
Total functional disability, as well as the subdomains of social life and family life/home responsibilities, significantly moderated response to IV ketamine (p = .003; p = .008; p = .008). Follow-up simple slopes analyses indicated a significant improvement in depressive symptoms across the functional domain spectrum (ps < .001). Above average functional disability (i.e., 1 SD > mean functional impairment within the sample) was associated with a greater change in depressive symptoms. Workplace function did not significantly moderate response to IV ketamine (p = .307), suggesting that individuals with significantly impaired workplace functioning may expect a similar response to ketamine as those with less workplace impairment.
Symptomatic benefit with IV ketamine was observed in patients with TRD and significant pre-treatment functional impairment. The foregoing result has implications for mechanism of action, cost-effectiveness, and patient selection in adults with TRD receiving IV ketamine.
在有更大治疗前功能障碍的患者中,基于单胺的抗抑郁药治疗成年人重度抑郁症(MDD)的疗效减弱。在此,我们研究了治疗抵抗性抑郁症(TRD)门诊患者的治疗前功能是否调节对静脉(IV)氯胺酮的反应。
符合 DSM-5 定义的 MDD 或双相障碍和 TRD 的成年人(N=326;M=45)在社区诊所接受重复剂量 IV 氯胺酮治疗。使用 Sheehan 残疾量表(SDS)评估功能,采用总分以及工作场所/学校、社会生活和家庭生活/家庭责任等亚域的分数。主要的因变量是从治疗前到输注后 4 时的抑郁症状变化,使用快速抑郁症状自评量表-自我报告 16 进行评估。
总功能障碍以及社会生活和家庭生活/家庭责任等亚域显著调节了 IV 氯胺酮的反应(p=0.003;p=0.008;p=0.008)。随访简单斜率分析表明,在整个功能域谱上抑郁症状都有显著改善(p<0.001)。高于平均的功能障碍(即,样本中平均功能障碍的 1 个标准差以上)与抑郁症状的变化更大相关。工作场所功能未显著调节 IV 氯胺酮的反应(p=0.307),这表明功能明显受损的工作场所的患者可能与功能受损较小的患者对氯胺酮有相似的反应。
在 TRD 且有显著治疗前功能障碍的患者中观察到 IV 氯胺酮的症状改善。上述结果对接受 IV 氯胺酮治疗的 TRD 成人的作用机制、成本效益和患者选择具有影响。