Maihöfner Christian, Forster Clemens, Birklein Frank, Neundörfer Bernhard, Handwerker Hermann O
Department of Neurology, University of Erlangen-Nuremberg, Schwabachanlage 6, 91054 Erlangen, Germany.
Pain. 2005 Mar;114(1-2):93-103. doi: 10.1016/j.pain.2004.12.001. Epub 2005 Jan 26.
Complex Regional Pain Syndromes (CRPS) are characterized by a triad of sensory, motor and autonomic dysfunctions of still unknown origin. Pain and mechanical hyperalgesia are hallmarks of CRPS. There are several lines of evidence that central nervous system (CNS) changes are crucial for the development and maintenance of mechanical hyperalgesia. However, little is known about the cortical structures associated with the processing of hyperalgesia in pain patients. This study describes the use of functional magnetic resonance imaging (fMRI) to delineate brain activations during pin-prick hyperalgesia in CRPS. Twelve patients, in whom previous quantitative sensory testing revealed the presence of hyperalgesia to punctuate mechanical stimuli (i.e. pin-prick hyperalgesia), were included in the study. Pin-prick-hyperalgesia was elicited by von-Frey filaments at the affected limb. For control, the identical stimulation was performed on the unaffected limb. fMRI was used to explore the corresponding cortical activations. Mechanical stimulation at the unaffected limb was non-painful and mainly led to an activation of the contralateral primary somatosensory cortex (S1), insula and bilateral secondary somatosensory cortices (S2). The stimulation of the affected limb was painful (mechanical hyperalgesia) and led to a significantly increased activation of the S1 cortex (contralateral), S2 (bilateral), insula (bilateral), associative-somatosensory cortices (contralateral), frontal cortices and parts of the anterior cingulate cortex. The results of our study indicate a complex cortical network activated during pin-prick hyperalgesia in CRPS. The underlying neuronal matrix comprises areas not only involved in nociceptive, but also in cognitive and motor processing.
复杂性区域疼痛综合征(CRPS)的特征是存在三联征,即感觉、运动和自主神经功能障碍,但其病因仍不明。疼痛和机械性痛觉过敏是CRPS的标志。有几条证据表明,中枢神经系统(CNS)的变化对于机械性痛觉过敏的发生和维持至关重要。然而,对于疼痛患者中与痛觉过敏处理相关的皮质结构知之甚少。本研究描述了使用功能磁共振成像(fMRI)来描绘CRPS患者针刺性痛觉过敏期间的脑激活情况。12名患者被纳入研究,之前的定量感觉测试显示他们对点状机械刺激(即针刺性痛觉过敏)存在痛觉过敏。通过用von-Frey细丝刺激患侧肢体诱发针刺性痛觉过敏。作为对照,在未受影响的肢体上进行相同的刺激。使用fMRI来探索相应的皮质激活情况。对未受影响肢体的机械刺激不引起疼痛,主要导致对侧初级躯体感觉皮层(S1)、脑岛和双侧次级躯体感觉皮层(S2)的激活。对患侧肢体的刺激是疼痛的(机械性痛觉过敏),并导致S1皮层(对侧)、S2(双侧)、脑岛(双侧)、联合躯体感觉皮层(对侧)、额叶皮层和前扣带回皮层部分区域的激活显著增加。我们的研究结果表明,CRPS患者在针刺性痛觉过敏期间激活了一个复杂的皮质网络。潜在的神经元基质不仅包括参与伤害性感受的区域,还包括参与认知和运动处理的区域。