功能性神经障碍和慢性疼痛的共享神经特征:多模态叙事回顾。

IF 2.1 Q3 CLINICAL NEUROLOGY
BMJ Neurology Open Pub Date : 2025-07-13 eCollection Date: 2025-01-01 DOI:10.1136/bmjno-2025-001032
Siddarth Kannan, Kajal Patel, Daniela Di Basilio, Antonia Kirkby, Manoj Sivan, Anthony Jones, Rajiv Mohanraj, Abhijit Das
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引用次数: 0

摘要

背景:功能性神经障碍(FND)经常与慢性疼痛(CP)共存,特别是伤害性和伤害性(原发性)疼痛障碍。由于其相似的临床和流行病学概况,相当大的重叠意味着共享的潜在机制。虽然标准的神经成像和电生理测试通常在FND和原发性疼痛疾病中显示正常结果,但最近神经成像技术的进步已经开始识别这两种疾病共同的神经生物标志物,尽管这些发现仍处于初步阶段,需要进一步探索。方法:采用脑电图、脑磁图、功能磁共振成像、正电子发射断层扫描和单光子发射计算机断层扫描等方法,对FND和慢性疼痛的神经活动进行了详细的文献回顾。鉴于所审查的研究的多样性,综合呈现叙述。结果:尽管方法上存在差异,但聚合数据表明FND和CP的神经网络都受到了破坏。共同的发现包括:(1)感觉运动网络的过度激活,(2)默认模式网络(自我参照思维的关键区域)的活动改变,(3)情绪处理区域的功能障碍,尤其是前扣带皮层和脑岛。丘脑皮质节律异常被认为是一个潜在的统一概念,其特征是异常的θ波和β波振荡增强CP的痛觉,并引发FND的功能性症状。这两种情况都表现出减少的α振荡,可能会放大感官敏感性和情绪反应。结论:这篇综述强调了共同的神经异常(三重网络模型),并将丘脑皮质节律异常作为一种新的解释框架,将FND和CP联系起来。未来的研究应该针对共存疾病的人群,为创新治疗铺平道路,包括催眠和神经调节/神经反馈。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Shared neural signatures in Functional Neurological Disorder and Chronic Pain: a multimodal narrative review.

Background: Functional neurological disorder (FND) frequently co-exists with chronic pain (CP), notably nociceptive and nociplastic (primary) pain disorders. The considerable overlap implies shared underlying mechanisms because of their similar clinical and epidemiological profiles. Although standard neuroimaging and electrophysiological tests typically show normal results in both FND and primary pain disorders, recent advancements in neuroimaging techniques have begun identifying neural biomarkers common to both conditions, though these findings remain preliminary and require further exploration.

Method: We performed a detailed literature review of studies investigating neural activity in FND and chronic pain using electroencephalogram, magneto-encephalography, functional MRI, positron emission tomography and single photon emission computed tomography. Given the diverse nature of the reviewed studies, the synthesis is presented narratively.

Results: Despite methodological differences, convergent data suggest disrupted neural networks across both FND and CP. Common findings include (1) hyperactivation of sensorimotor networks, (2) altered activity within the default mode network-a critical region for self-referential thought-and (3) dysfunction in emotional processing regions, notably the anterior cingulate cortex and insula. Thalamocortical dysrhythmia was identified as a potential unifying concept, characterised by abnormal theta and beta oscillations that enhance pain perception in CP and trigger functional symptoms in FND. Both conditions also exhibit reduced alpha oscillations, likely amplifying sensory sensitivity and emotional responsiveness.

Conclusion: This review highlights shared neural abnormalities (Triple Network model) and introduces thalamocortical dysrhythmia as a novel explanatory framework linking FND and CP. Future research should target populations with coexisting disorders, potentially paving the way for innovative treatments, including hypnosis and neuromodulation/neurofeedback.

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来源期刊
BMJ Neurology Open
BMJ Neurology Open Medicine-Neurology (clinical)
CiteScore
3.20
自引率
3.70%
发文量
46
审稿时长
13 weeks
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