Minzenberg Michael J, Yoon Jong H, Cheng Yaoan, Carter Cameron S
Department of Psychiatry, University of California, San Francisco School of Medicine, and San Francisco Veterans Affairs Medical Center, San Francisco, CA, USA.
Department of Psychiatry, Stanford University School of Medicine, and Palo Alto Veterans Affairs Medical Center, Palo Alto, CA, USA.
Neuropsychopharmacology. 2016 Apr;41(5):1231-40. doi: 10.1038/npp.2015.271. Epub 2015 Sep 2.
Control-related cognitive processes such as rule selection and maintenance are associated with cortical oscillations in the gamma range, and modulated by catecholamine neurotransmission. Control-related gamma power is impaired in schizophrenia, and an understudied treatment target. It remains unknown whether pro-catecholamine pharmacological agents augment control-related gamma oscillations in schizophrenia. We tested the effects of 4-week fixed-dose daily adjunctive modafinil (MOD) 200 mg, in a randomized double-blind, placebo-controlled, parallel-groups design. Twenty-seven stable schizophrenia patients performed a cognitive control task during EEG, at baseline and after 4 weeks of treatment. EEG data underwent time-frequency decomposition with Morlet wavelets to determine power of 4-80 Hz oscillations. The modafinil group (n=14), relative to placebo group (n=13), exhibited enhanced oscillatory power associated with high-control rule selection in the gamma range after treatment, with additional effects during rule maintenance in gamma and sub-gamma ranges. MOD-treated patients who exhibited improved task performance with treatment also showed greater treatment-related delay period gamma compared with MOD-treated patients without improved performance. This is the first evidence in schizophrenia of augmentation of cognition-related gamma oscillations by an FDA-approved agent with therapeutic potential. Gamma oscillations represent a novel treatment target in this disorder, and modulation of catecholamine signaling may represent a viable strategy at this target.
与控制相关的认知过程,如规则选择和维持,与伽马范围内的皮层振荡相关,并受儿茶酚胺神经传递的调节。与控制相关的伽马功率在精神分裂症中受损,是一个研究不足的治疗靶点。目前尚不清楚儿茶酚胺类药物是否能增强精神分裂症患者与控制相关的伽马振荡。我们采用随机双盲、安慰剂对照、平行组设计,测试了为期4周、每日固定剂量200毫克的阿得拉(MOD)的效果。27名病情稳定的精神分裂症患者在脑电图监测下,于基线期和治疗4周后进行认知控制任务。脑电图数据采用Morlet小波进行时频分解,以确定4-80赫兹振荡的功率。与安慰剂组(n=13)相比,阿得拉组(n=14)在治疗后,与高控制规则选择相关的伽马范围内的振荡功率增强,在伽马和亚伽马范围内的规则维持过程中还有额外效果。与治疗后任务表现未改善的阿得拉治疗患者相比,治疗后任务表现改善的阿得拉治疗患者在与治疗相关的延迟期伽马方面也表现出更强的功率。这是FDA批准的具有治疗潜力的药物增强精神分裂症患者认知相关伽马振荡的首个证据。伽马振荡是这种疾病的一个新的治疗靶点,调节儿茶酚胺信号可能是针对这个靶点的一个可行策略。