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Multiple Imputation for Multivariate Missing-Data Problems: A Data Analyst's Perspective.多元缺失数据问题的多重填补:数据分析师视角
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Paired associative stimulation increases motor cortex excitability more effectively than theta-burst stimulation.配对联想刺激比 theta 爆发刺激更有效地增加运动皮层兴奋性。
Clin Neurophysiol. 2012 Nov;123(11):2220-6. doi: 10.1016/j.clinph.2012.03.081. Epub 2012 May 18.
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Exploring the effect of inducing long-term potentiation in the human motor cortex on motor learning.探索在人类运动皮层诱导长时程增强对运动学习的影响。
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Distinct maturation profiles of perisomatic and dendritic targeting GABAergic interneurons in the mouse primary visual cortex during the critical period of ocular dominance plasticity.在视主导可塑性的关键期,小鼠初级视觉皮层中,囊泡靶向和树突靶向 GABA 能中间神经元表现出不同的成熟模式。
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Correlation between cortical plasticity, motor learning and BDNF genotype in healthy subjects.健康受试者皮质可塑性、运动学习与 BDNF 基因型的相关性。
Exp Brain Res. 2011 Jul;212(1):91-9. doi: 10.1007/s00221-011-2700-5. Epub 2011 May 3.
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GABA-related transcripts in the dorsolateral prefrontal cortex in mood disorders.心境障碍患者外侧前额叶皮质中的 GABA 相关转录本。
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Decreased BDNF, trkB-TK+ and GAD67 mRNA expression in the hippocampus of individuals with schizophrenia and mood disorders.精神分裂症和心境障碍患者海马脑源性神经营养因子、trkB-TK+ 和 GAD67mRNA 表达降低。
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抑郁个体与健康对照者的神经可塑性比较。

Neuroplasticity in depressed individuals compared with healthy controls.

机构信息

1] School of Psychiatry, University of New South Wales, Sydney, NSW, Australia [2] Black Dog Institute, Sydney, NSW, Australia.

出版信息

Neuropsychopharmacology. 2013 Oct;38(11):2101-8. doi: 10.1038/npp.2013.126. Epub 2013 May 16.

DOI:10.1038/npp.2013.126
PMID:23676792
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3773676/
Abstract

Several lines of evidence suggest that neuroplasticity is impaired in depression. This study aimed to compare neuroplasticity in 23 subjects with DSM-IV major depressive episode and 23 age- and gender-matched healthy controls, using an objective test that is independent of subject effort and motivation. Neuroplasticity was assessed in the motor cortex using a brain stimulation paradigm known as paired associative stimulation (PAS), which induces transient changes in motor cortical function. Motor cortical excitability was assessed before and after PAS using single-pulse transcranial magnetic stimulation (TMS) to induce motor evoked potentials (MEPs) in a hand muscle. After PAS, MEP amplitudes significantly increased in healthy controls compared with depressed subjects (P=0.002). The functional significance of motor cortical changes was assessed using a motor learning task-a computerized version of the rotor pursuit task. Healthy controls also performed better on motor learning (P=0.02). BDNF blood levels and genotype were assayed to determine any relationship with motor cortical plasticity. However, PAS results did not correlate with motor learning, nor appear to be related to BDNF measures. The significance of these findings is that it provides one of the first direct demonstrations of reduced neuroplasticity in depressed subjects, using an objective test.

摘要

有几条证据表明,抑郁症患者的神经可塑性受到损害。本研究旨在使用一种客观的测试方法来比较 23 名符合 DSM-IV 重性抑郁发作的患者和 23 名年龄和性别匹配的健康对照者的神经可塑性,这种测试方法独立于被试的努力和动机。通过一种称为配对关联刺激(PAS)的脑刺激范式来评估运动皮层的神经可塑性,该范式可引起运动皮层功能的短暂变化。使用单脉冲经颅磁刺激(TMS)在手肌肉中诱发运动诱发电位(MEPs),在 PAS 之前和之后评估运动皮层兴奋性。与抑郁患者相比,健康对照组在 PAS 后 MEP 幅度明显增加(P=0.002)。使用运动学习任务(转子追踪任务的计算机版本)评估运动皮层变化的功能意义。健康对照组在运动学习方面也表现更好(P=0.02)。测定了 BDNF 血液水平和基因型,以确定其与运动皮层可塑性的任何关系。然而,PAS 的结果与运动学习无关,也似乎与 BDNF 测量无关。这些发现的意义在于,它提供了使用客观测试方法首次直接证明抑郁患者神经可塑性降低的证据之一。