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创伤性脑损伤中的主动反应抑制与皮质下灰质完整性

Proactive Response Inhibition and Subcortical Gray Matter Integrity in Traumatic Brain Injury.

作者信息

Hermans Lize, Beeckmans Kurt, Michiels Karla, Lafosse Christophe, Sunaert Stefan, Coxon James P, Swinnen Stephan P, Leunissen Inge

机构信息

1 Movement Control and Neuroplasticity Research Group, Biomedical Sciences Group, KU Leuven, Belgium.

2 Center for Epilepsy and Acquired Brain Injury (CEPOS), Duffel, Belgium.

出版信息

Neurorehabil Neural Repair. 2017 Mar;31(3):228-239. doi: 10.1177/1545968316675429. Epub 2016 Oct 28.

Abstract

BACKGROUND

Traumatic brain injury (TBI) has been associated with impairments in inhibiting prepotent motor responses triggered by infrequent external signals (ie, reactive inhibition). It is unclear whether proactive preparation to inhibit upcoming responses is also affected (ie, proactive inhibition). Successful inhibition relies on frontosubcortical interactions; therefore, impairments might be linked with gray matter atrophy in subcortical structures.

OBJECTIVE

We investigated reactive and proactive inhibition in TBI and control groups, and their relationship with subcortical gray matter.

METHODS

Participants performed a response inhibition task in which the probability of stopping was manipulated. Reactive inhibition was measured as the stop-signal reaction time (SSRT) when the probability of stopping was low. Proactive inhibition was measured as the change in SSRT and in go response time with increasing probability of stopping. Subcortical gray matter structures were automatically segmented with FSL-FIRST. Group differences in subregional volume and associations with reactive and proactive inhibition efficiency were investigated using shape analysis.

RESULTS

Reactive inhibition was impaired in TBI, as indicated by longer SSRTs. Moreover, the degree of atrophy in subregions of subcortical structures was predictive for SSRT in TBI. In contrast, proactive inhibition was not affected because both groups showed no response time slowing as a function of stopping probability. Proactive inhibition efficiency could be predicted by local volume in the anterior left putamen, bilateral pallidum, and right thalamus in controls but not in TBI.

CONCLUSIONS

Our results reveal that proactive inhibition seems unaffected in TBI and that volume of subregions of subcortical nuclei is predictive for response inhibition proficiency and of clinical relevance in TBI.

摘要

背景

创伤性脑损伤(TBI)与抑制由不常见外部信号触发的优势运动反应(即反应性抑制)受损有关。尚不清楚对即将到来的反应进行主动抑制准备是否也会受到影响(即主动性抑制)。成功的抑制依赖于额叶皮质下相互作用;因此,损伤可能与皮质下结构的灰质萎缩有关。

目的

我们研究了TBI组和对照组的反应性和主动性抑制,以及它们与皮质下灰质的关系。

方法

参与者执行一项反应抑制任务,其中停止的概率是可操纵的。当停止概率较低时,反应性抑制通过停止信号反应时间(SSRT)来衡量。主动性抑制通过随着停止概率增加SSRT和去反应时间的变化来衡量。使用FSL-FIRST自动分割皮质下灰质结构。使用形状分析研究亚区域体积的组间差异以及与反应性和主动性抑制效率的关联。

结果

TBI组的反应性抑制受损,表现为SSRT更长。此外,皮质下结构亚区域的萎缩程度可预测TBI组的SSRT。相比之下,主动性抑制未受影响,因为两组均未表现出反应时间随停止概率而减慢。在对照组中,主动性抑制效率可通过左侧前壳核、双侧苍白球和右侧丘脑的局部体积来预测,但在TBI组中则不然。

结论

我们的结果表明,TBI患者的主动性抑制似乎未受影响,皮质下核团亚区域的体积可预测反应抑制能力及TBI的临床相关性。

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