Defrin Ruth, Devor Marshall, Brill Silviu
Department of Physical Therapy, School of Allied Health Professions, The Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv 69978, Israel Department of Cell and Developmental Biology, Institute of Life Sciences, and Center for Research on Pain, The Hebrew University of Jerusalem, Jerusalem 91904, Israel Institute of Pain Medicine, Department of Anesthesia and Critical Care Medicine, Tel Aviv Sourasky Medical Center, Sackler Faculty of Medicine, Tel Aviv University, Tel-Aviv 69978, Israel.
Pain. 2014 Dec;155(12):2551-2559. doi: 10.1016/j.pain.2014.09.015. Epub 2014 Sep 19.
We report a novel symptom in many patients with low back pain (LBP) that sheds new light on the underlying pain mechanism. By means of quantitative sensory testing, we compared patients with radicular LBP (sciatica), axial LBP (LBP without radiation into the leg), and healthy controls, searching for cutaneous allodynia in response to weak tactile and cooling stimuli on the leg and low back. Most patients with radicular pain (~60%) reported static and dynamic tactile allodynia, as well as cooling allodynia, on the leg, often extending into the foot. Some also reported allodynia on the low back. In axial LBP, allodynia was almost exclusively on the back. The degree of dynamic tactile allodynia correlated with the degree of background pain. The presence of allodynia suggests that the peripheral nerve generators of background leg and back pain have also induced central sensitization. The distal (foot) location of the allodynia in patients who have it indicates that the nociceptive drive that maintains the central sensitization arises paraspinally (ectopically) in injured ventral ramus afferents; this is not an instance of somatic referred pain. The presence of central sensitization also provides the first cogent account of shooting pain in sciatica as a wave of activity sweeping vectorially across the width of the sensitized dorsal horn. Finally, the results endorse leg allodynia as a pain biomarker in animal research on LBP, which is commonly used but has not been previously validated. In addition to informing the underlying mechanism of LBP, bedside mapping of allodynia might have practical implications for prognosis and treatment.
How can you tell whether pain radiating into the leg in a patient with sciatica is neuropathic, ie, due to nerve injury?
我们报告了许多腰痛(LBP)患者出现的一种新症状,这为潜在的疼痛机制提供了新线索。通过定量感觉测试,我们比较了根性腰痛(坐骨神经痛)患者、轴性腰痛(无腿部放射痛的腰痛)患者和健康对照者,寻找腿部和下背部对微弱触觉和冷刺激产生的皮肤异常性疼痛。大多数根性疼痛患者(约60%)报告腿部存在静态和动态触觉异常性疼痛以及冷异常性疼痛,且常延伸至足部。一些患者还报告下背部有异常性疼痛。在轴性腰痛患者中,异常性疼痛几乎仅出现在背部。动态触觉异常性疼痛的程度与背景疼痛程度相关。异常性疼痛的存在表明腿部和背部疼痛的周围神经发生器也诱发了中枢敏化。有异常性疼痛的患者其异常性疼痛位于远端(足部),这表明维持中枢敏化的伤害性驱动源自受损腹侧支传入神经的椎旁(异位)部位;这并非躯体牵涉痛的情况。中枢敏化的存在也首次有力地解释了坐骨神经痛中的刺痛是一股活动波沿致敏背角宽度矢量扫过。最后,这些结果支持腿部异常性疼痛作为腰痛动物研究中的一种疼痛生物标志物,该标志物虽常用但此前未经验证。除了为腰痛的潜在机制提供信息外,异常性疼痛的床边定位可能对预后和治疗具有实际意义。
如何判断坐骨神经痛患者放射至腿部的疼痛是否为神经性疼痛,即是否由神经损伤引起?