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托卡朋增强健康成年人的神经认知:神经基础与预测因素

Tolcapone-Enhanced Neurocognition in Healthy Adults: Neural Basis and Predictors.

作者信息

Bhakta Savita G, Light Gregory A, Talledo Jo A, Balvaneda Bryan, Hughes Erica, Alvarez Alexis, Rana Brinda K, Young Jared W, Swerdlow Neal R

机构信息

Department of Psychiatry, University of California, San Diego, La Jolla, California; Research Service MIRECC, VISN 22, Veterans Affairs San Diego Healthcare System, San Diego, California.

出版信息

Int J Neuropsychopharmacol. 2017 Dec 1;20(12):979-987. doi: 10.1093/ijnp/pyx074.

Abstract

BACKGROUND

Failure of procognitive drug trials in schizophrenia may reflect the clinical heterogeneity of schizophrenia, underscoring the need to identify biomarkers of treatment sensitivity. We used an experimental medicine design to test the procognitive effects of a putative procognitive agent, tolcapone, using an electroencephalogram-based cognitive control task in healthy subjects.

METHODS

Healthy men and women (n=27; ages 18-35 years), homozygous for either the Met/Met or Val/Val rs4680 genotype, received placebo and tolcapone 200 mg orally across 2 test days separated by 1 week in a double-blind, randomized, counterbalanced, within-subject design. On each test day, neurocognitive performance was assessed using the MATRICS Consensus Cognitive Battery and an electroencephalogram-based 5 Choice-Continuous Performance Test.

RESULTS

Tolcapone enhanced visual learning in low-baseline MATRICS Consensus Cognitive Battery performers (d=0.35) and had an opposite effect in high performers (d=0.5), and enhanced verbal fluency across all subjects (P=.03) but had no effect on overall MATRICS Consensus Cognitive Battery performance. Tolcapone reduced false alarm rate (d=0.8) and enhanced frontal P200 amplitude during correctly identified nontarget trials (d=0.6) in low-baseline 5 Choice-Continuous Performance Test performers and had opposite effects in high performers (d=0.5 and d=0.25, respectively). Tolcapone's effect on frontal P200 amplitude and false alarm rate was correlated (rs=-0.4, P=.05). All neurocognitive effects of tolcapone were independent of rs4680 genotype.

CONCLUSION

Tolcapone enhanced neurocognition and engaged electroencephalogram measures relevant to cognitive processes in specific subgroups of healthy individuals. These findings support an experimental medicine model for identifying procognitive treatments and provide a strong basis for future biomarker-informed procognitive studies in schizophrenia patients.

摘要

背景

治疗精神分裂症的促认知药物试验失败可能反映了精神分裂症的临床异质性,这突出了识别治疗敏感性生物标志物的必要性。我们采用实验医学设计,在健康受试者中使用基于脑电图的认知控制任务,来测试一种假定的促认知药物托卡朋的促认知作用。

方法

27名年龄在18 - 35岁之间、基因型为纯合子Met/Met或Val/Val rs4680的健康男性和女性,在一项双盲、随机、平衡、受试者内设计中,于相隔1周的2个测试日口服安慰剂和200毫克托卡朋。在每个测试日,使用MATRICS共识认知成套测验和基于脑电图的5选持续性操作测验评估神经认知表现。

结果

托卡朋增强了MATRICS共识认知成套测验低基线表现者的视觉学习能力(d = 0.35),而对高表现者有相反作用(d = 0.5),并增强了所有受试者的言语流畅性(P = 0.03),但对MATRICS共识认知成套测验的总体表现没有影响。托卡朋降低了低基线5选持续性操作测验表现者在正确识别的非目标试验中的误报率(d = 0.8),并增强了额叶P200波幅(d = 0.6),而对高表现者有相反作用(分别为d = 0.5和d = 0.25)。托卡朋对额叶P200波幅和误报率的影响具有相关性(rs = -0.4,P = 0.05)。托卡朋的所有神经认知作用均与rs4680基因型无关。

结论

托卡朋增强了神经认知,并在健康个体的特定亚组中影响了与认知过程相关的脑电图指标。这些发现支持了一种用于识别促认知治疗的实验医学模型,并为未来在精神分裂症患者中开展基于生物标志物的促认知研究提供了有力依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c30c/5716101/3839c8caabbb/pyx07401.jpg

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