复杂区域性疼痛综合征和慢性腰痛的感觉表型-共同潜在病理机制的指征。

IF 3.4 Q2 NEUROSCIENCES
Pain Reports Pub Date : 2023-11-15 eCollection Date: 2023-12-01 DOI:10.1097/PR9.0000000000001110
Iara De Schoenmacker, Laura Sirucek, Paulina S Scheuren, Robin Lütolf, Lindsay M Gorrell, Florian Brunner, Armin Curt, Jan Rosner, Petra Schweinhardt, Michèle Hubli
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引用次数: 0

摘要

超过50%的慢性疼痛患者的一线疼痛治疗不满意,可能是因为疼痛慢性化机制的异质性。目的:本横断面研究旨在通过聚类分析确定不同的感觉表型,从而更好地了解不同慢性疼痛人群的病理机制,而不管他们的诊断如何。方法:我们招募了81例慢性疼痛患者和63例年龄和性别匹配的健康对照(HC)。招募了两个不同的慢性疼痛队列,即复杂局部疼痛综合征(N = 20)和腰痛(N = 61)。定量感觉测试(QST)在最疼痛的身体区域进行,以调查与临床疼痛相关的体感觉变化。此外,QST是在无痛区域进行的,以确定远程感觉的变化,表明在体感处理中更广泛的变化。结果:根据疼痛区域的QST测量确定了两个集群,它们不代表2种不同的疼痛诊断,但包含了两个队列的患者。集群1显示疼痛区和控制区疼痛敏感性增加,表明中枢致敏可能是一种潜在的病理机制。集群2在两个测试区域显示出与HC相似的感觉轮廓。因此,要么QST不够敏感,需要更客观的措施来检测伤害神经轴或簇2的致敏性,可能主要是因为致敏性而没有疼痛,但其他因素如心理社会因素也参与其中。结论:这些发现支持了与疼痛诊断无关的共同病理机制的概念。相反,不同的机制可能导致相同诊断的患者疼痛。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sensory phenotypes in complex regional pain syndrome and chronic low back pain-indication of common underlying pathomechanisms.

Introduction: First-line pain treatment is unsatisfactory in more than 50% of chronic pain patients, likely because of the heterogeneity of mechanisms underlying pain chronification.

Objectives: This cross-sectional study aimed to better understand pathomechanisms across different chronic pain cohorts, regardless of their diagnoses, by identifying distinct sensory phenotypes through a cluster analysis.

Methods: We recruited 81 chronic pain patients and 63 age-matched and sex-matched healthy controls (HC). Two distinct chronic pain cohorts were recruited, ie, complex regional pain syndrome (N = 20) and low back pain (N = 61). Quantitative sensory testing (QST) was performed in the most painful body area to investigate somatosensory changes related to clinical pain. Furthermore, QST was conducted in a pain-free area to identify remote sensory alterations, indicating more widespread changes in somatosensory processing.

Results: Two clusters were identified based on the QST measures in the painful area, which did not represent the 2 distinct pain diagnoses but contained patients from both cohorts. Cluster 1 showed increased pain sensitivities in the painful and control area, indicating central sensitization as a potential pathomechanism. Cluster 2 showed a similar sensory profile as HC in both tested areas. Hence, either QST was not sensitive enough and more objective measures are needed to detect sensitization within the nociceptive neuraxis or cluster 2 may not have pain primarily because of sensitization, but other factors such as psychosocial ones are involved.

Conclusion: These findings support the notion of shared pathomechanisms irrespective of the pain diagnosis. Conversely, different mechanisms might contribute to the pain of patients with the same diagnosis.

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来源期刊
Pain Reports
Pain Reports Medicine-Anesthesiology and Pain Medicine
CiteScore
7.50
自引率
2.10%
发文量
93
审稿时长
8 weeks
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