Experimental Therapeutics and Pathophysiology Branch, National Institute of Mental Health, National Institutes of Health, Bethesda, Maryland 20892, USA.
JAMA Psychiatry. 2013 Mar;70(3):280-90. doi: 10.1001/2013.jamapsychiatry.60.
The need for improved treatment options for patients with major depressive disorder (MDD) is critical. Faster-acting antidepressants and biomarkers that predict clinical response will facilitate treatment. Scopolamine produces rapid antidepressant effects and thus offers the opportunity to characterize potential biomarkers of treatment response within short periods.
To determine if baseline brain activity when processing emotional information can predict treatment response to scopolamine in MDD.
A double-blind, placebo-controlled, crossover study together with repeated functional magnetic resonance imaging, acquired as participants performed face-identity and face-emotion working memory tasks.
National Institute of Mental Health Division of Intramural Research Programs.
Fifteen currently depressed outpatients meeting DSM-IV criteria for recurrent MDD and 21 healthy participants, between 18 and 55 years of age.
The magnitude of treatment response to scopolamine (percentage of change in the Montgomery-Asberg Depression Rating Scale score between study end and baseline) was correlated with blood oxygen level-dependent (BOLD) signal associated with each working memory component (encode, maintenance, and test) for both identity and emotion tasks. Treatment response also was correlated with change in BOLD response (scopolamine vs baseline). Baseline activity was compared between healthy and MDD groups.
Baseline BOLD response in the bilateral middle occipital cortex, selectively during the stimulus-processing components of the emotion working memory task (no correlation during the identity task), correlated with treatment response magnitude. Change in BOLD response following scopolamine administration in overlapping areas in the middle occipital cortex while performing the same task conditions also correlated with clinical response. Healthy controls showed higher activity in the same visual regions than patients with MDD during baseline.
These results implicate cholinergic and visual processing dysfunction in the pathophysiology of MDD and suggest that neural response in the visual cortex, selectively to emotional stimuli, may provide a useful biomarker for identifying patients who will respond favorably to scopolamine.
clinicaltrials.gov Identifier: NCT00055575.
对于患有重度抑郁症(MDD)的患者,改善治疗选择至关重要。起效更快的抗抑郁药和预测临床反应的生物标志物将有助于治疗。东莨菪碱可产生快速的抗抑郁作用,因此有机会在短时间内确定治疗反应的潜在生物标志物。
确定处理情绪信息时的基线大脑活动是否可以预测 MDD 患者对东莨菪碱的治疗反应。
一项双盲、安慰剂对照、交叉研究,同时进行重复功能磁共振成像,参与者在执行面孔身份和面孔情绪工作记忆任务时进行。
美国国立卫生研究院精神分裂症与神经发育障碍分部。
15 名目前患有符合 DSM-IV 标准的复发性 MDD 的门诊患者和 21 名年龄在 18 至 55 岁之间的健康参与者。
东莨菪碱治疗反应的幅度(研究结束时与基线相比,蒙哥马利-阿斯伯格抑郁评定量表评分的变化百分比)与身份和情绪任务的每个工作记忆成分(编码、维持和测试)相关的血氧水平依赖(BOLD)信号相关。治疗反应还与 BOLD 反应的变化(东莨菪碱与基线相比)相关。将健康组和 MDD 组之间的基线活动进行比较。
双侧中枕叶皮层在情绪工作记忆任务的刺激处理成分期间的基线 BOLD 反应(在身份任务期间无相关性)与治疗反应幅度相关。在执行相同任务条件时,中枕叶皮层重叠区域中给予东莨菪碱后 BOLD 反应的变化也与临床反应相关。在基线时,健康对照组在相同的视觉区域表现出比 MDD 患者更高的活动。
这些结果表明,MDD 的病理生理学中存在胆碱能和视觉处理功能障碍,并表明视觉皮层对情绪刺激的神经反应可能提供一种有用的生物标志物,用于识别对东莨菪碱反应良好的患者。
clinicaltrials.gov 标识符:NCT00055575。