神经生理病变:范围综述

David N. Taylor DC
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引用次数: 0

摘要

目的本研究的目的是检查功能神经学中有关神经生理病变的文献的参考程度。方法检索2010年至2021年3月的文献。搜索词包括中枢敏化、中枢敏化综合征、致伤性疼痛、冷痛觉过敏、热痛觉过敏、机械性痛觉过敏、动态机械异常性痛、时间汇总、空间汇总和下行抑制。定性综合总结了研究结果,包括脊柱推拿的临床条件和效果。结果共纳入30项研究,其中7项高水平研究(荟萃分析或系统评价),22项随机对照研究,1项范围评价。研究结果表明,在各种紊乱、实验诱导的刺激和治疗的神经元群体中,存在中枢整合状态的变化。目前的文献表明,中央整合状态(CIS)随着病理的发生而具有可塑性,并且不同的保守非药物治疗会改变CIS。结论本综述提示生理性损伤中存在的一群神经元的CIS静息状态的变化可能会随着包括手法治疗在内的各种治疗而改变。本综述的研究结果支持了非药物性保守治疗可能影响神经生理病变的假设。然而,研究是异质性的,缺乏证据表明靶向治疗不同神经元区域的临床结果可以治疗特定的疾病状态。
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The Neurophysiological Lesion: A Scoping Review

Objective

The purpose of this study was to examine the extent of the literature on the neurophysiological lesion as referenced in functional neurology.

Methods

A literature search was performed within the period from 2010 to March 2021. Search terms included central sensitization, central sensitivity syndrome, nociplastic pain, cold hyperalgesia, heat hyperalgesia, mechanical hyperalgesia, dynamic mechanical allodynia, temporal summation, spatial summation, and descending inhibition. A qualitative synthesis summarized the research findings, including clinical conditions and effect of spinal manipulation.

Results

There were 30 studies, which included 7 high-level studies (meta-analysis or systematic reviews), 22 randomized controlled studies, and 1 scoping review. The findings suggest the existence of the changes in the central integrated state of a population of neurons with various disorders, experimentally induced stimulation, and treatment. The current literature suggests plasticity of the central integrative state (CIS) with the onset of pathologies and the changes in the CIS with different conservative nonpharmacologic treatments.

Conclusions

This review suggests changes in the resting state of the CIS of a population of neurons that exist in the physiologic lesion may change in response to various therapies, including manipulative therapy. The findings from this review provide support of the hypothesis that nonpharmacologic conservative care may affect the neurophysiological lesion. However, studies were heterogeneous and evidence was lacking in the translation of targeting the therapies to distinct neuronal areas for clinical outcomes to treat specific disease states.

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