Center for Sensory-Motor Interaction (SMI), Department of Health Science and Technology, Aalborg University, DK-9220 Aalborg E, Denmark.
Nat Rev Rheumatol. 2010 Oct;6(10):599-606. doi: 10.1038/nrrheum.2010.107. Epub 2010 Jul 27.
The aim of this Review is to give a short presentation of the manifestations, assessment methods, and mechanisms underlying localized and widespread musculoskeletal pain, deep somatic tissue hyperalgesia and chronification. Hyperalgesia can be explained by increased pain sensitivity of nociceptors located in deep tissue (peripheral sensitization) or by increased responses from dorsal horn neurons (central sensitization). The spreading of pain and sensitization is related to increased synaptic activity in central neurons and to changes in descending control from supraspinal centers. Manifestations related to the different aspects of sensitization can be assessed quantitatively using sensory tests, such as pressure algometry (quantitative palpation) and cuff-algometry. Repeated pressure stimulation can evaluate the degree of temporal summation, which is a proxy for the level of central sensitization, as is expanded referred muscle pain area. The transition of acute localized musculoskeletal pain into chronic widespread pain is related to the progression of peripheral and central sensitization. This sensitization for the chronification of pain should be assessed by adequate pain biomarkers. Furthermore, pain prevention should target early intervention strategies and new anti-hyperalgesic compounds should be developed.
本文旨在简要介绍局限性和广泛性肌肉骨骼疼痛、深部躯体组织痛觉过敏和慢性化的表现、评估方法和机制。痛觉过敏可以用位于深部组织的伤害感受器的疼痛敏感性增加(外周致敏)或背角神经元的反应增加(中枢致敏)来解释。疼痛和敏化的扩散与中枢神经元突触活动的增加以及来自脊髓上中枢的下行控制的变化有关。可以使用感觉测试(如压力痛觉测定法(定量触诊)和袖带痛觉测定法)定量评估与敏化的不同方面相关的表现。重复压力刺激可评估时间总和的程度,这是中枢敏化程度的代表,扩大的牵涉性肌肉疼痛区域也是如此。急性局限性肌肉骨骼疼痛向慢性广泛性疼痛的转变与外周和中枢敏化的进展有关。这种疼痛慢性化的敏化应该通过适当的疼痛生物标志物来评估。此外,应该针对早期干预策略进行疼痛预防,并且应该开发新的抗痛觉过敏化合物。
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