Schlereth T, Heiland A, Breimhorst M, Féchir M, Kern U, Magerl W, Birklein F
Department of Neurology, University Medical Center, Mainz, Germany.
Eur J Pain. 2015 Feb;19(2):193-201. doi: 10.1002/ejp.537. Epub 2014 Jul 28.
In postherpetic neuralgia (PHN), dorsal root ganglia neurons are damaged. According to the proposed models, PHN pain might be associated with nociceptive deafferentation, and peripheral (heat hyperalgesia) or central sensitization (allodynia).
In 36 PHN patients, afferent nerve fibre function was characterized using quantitative sensory testing and histamine-induced flare analysis. Psychological factors were evaluated with the Hospital Anxiety and Depression Scale (HADS), disease-related quality of life (QoL) with SF-36 and pain with the McGill questionnaire [pain rating index (PRI)]. The patients were also divided into subgroups according to the presence or absence of brush-evoked allodynia as a sign of central sensitization.
For all patients, warm, cold and mechanical detection was impaired (p < 0.001 each) and the size of the histamine flare was diminished on the affected side (p < 0.05); pain thresholds with the exception of brush-evoked allodynia (p < 0.05) were unaltered. Correlation analysis revealed allodynia, anxiety, depression, QoL and age as relevant factors associated with pain severity (PRI). Allodynia was present in 23 patients (64%). In these patients, heat pain perception was preserved; the histamine flare was larger; the pinprick pain was increased as were McGill PRI sensory subscore, actual pain rating and almost significantly pain (McGill PRI) over the last 4 weeks.
PHN is associated with damage of afferent fibres. Central sensitization (i.e., allodynia) might contribute to PHN pain. There was a striking association between anxiety, depression and age, and the magnitude of PHN pain.
在带状疱疹后神经痛(PHN)中,背根神经节神经元受损。根据提出的模型,PHN疼痛可能与伤害性传入神经阻滞、外周(热痛觉过敏)或中枢敏化(异常性疼痛)有关。
对36例PHN患者,采用定量感觉测试和组胺诱发的红晕分析来表征传入神经纤维功能。使用医院焦虑抑郁量表(HADS)评估心理因素,使用SF-36评估疾病相关生活质量(QoL),使用麦吉尔问卷评估疼痛[疼痛评分指数(PRI)]。患者还根据是否存在作为中枢敏化标志的刷诱发异常性疼痛分为亚组。
对于所有患者,温觉、冷觉和机械觉检测均受损(各p<0.001)且患侧组胺诱发的红晕大小减小(p<0.05);除刷诱发异常性疼痛外(p<0.05)疼痛阈值未改变。相关分析显示,异常性疼痛、焦虑、抑郁、生活质量和年龄是与疼痛严重程度(PRI)相关的因素。23例患者(64%)存在异常性疼痛。在这些患者中热痛觉保留;组胺诱发的红晕更大;针刺疼痛增加,麦吉尔PRI感觉亚评分、实际疼痛评分以及过去4周内几乎显著的疼痛(麦吉尔PRI)也增加。
PHN与传入纤维损伤有关。中枢敏化(即异常性疼痛)可能导致PHN疼痛加剧。焦虑、抑郁和年龄与PHN疼痛程度之间存在显著关联关系。