Altun Idiris
Department of Neurosurgery, Medical Faculty, Kahramanmaras Sutcu Imam University, Kahramanmaras 46100, Turkey.
Spine J. 2016 Jul;16(7):857-61. doi: 10.1016/j.spinee.2016.03.019. Epub 2016 Mar 11.
Neuroinflammation is supposed to play a crucial role in the generation of chronic pain. Numerous trials have documented the contribution of proinflammatory cytokines in the pathophysiology of pain associated with peripheral and central nociception. Local and systemic expressions of proinflammatory cytokines have been implicated as mediators of pain. Among these cytokines, tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β), and interleukin-6 (IL-6) are especially notable because of their hyperalgesic impacts after nerve damage.
The aim of the present study was to evaluate and compare the tissue levels of IL-1β, IL-6, interleukin-10 (IL-10), and TNF-α in subligamentous and free fragment types of degenerated intervertebral disc in acute and chronic periods.
This was a cross-sectional study.
A cross-sectional study was implemented on a total of 49 patients (24 women, 25 men) with an average age of 38.2±4.9 treated surgically by means of microdiscectomy.
Of these cases, 19 had complaints for less than 6 months, whereas 30 patients had been suffering from low back pain and leg pain for more than 6 months. Thirty-eight patients have been diagnosed with subligamentous type and 11 patients had free fragment type of disc degeneration.
The levels of IL-1β, IL-6, IL-10, and TNF-α were assessed in tissue samples prepared from nucleus pulposus tissue obtained during microdiscectomy. Results were compared in patients with acute and chronic duration of complaints, as well as subligamentous and free fragment types of intervertebral disc degeneration.
The levels of IL-1β (p<.001), IL-6 (p<.001), IL-10 (p<.001), and TNF-α (p<.001) were significantly higher in patients with acute duration of complaints. Similarly, free fragment type of intervertebral disc degeneration displayed remarkably higher levels of IL-1β (p=.009), IL-6 (p<.001), IL-10 (p=.024), and TNF-α (p=.017) compared with the subligamentous type.
Inflammatory cytokines seem to have a more apparent role in intervertebral disc degeneration especially in acute period and in free fragment type. Further trials should be performed for elucidation of pathophysiology at the molecular level and the development of more effective diagnostic and therapeutic measures.
神经炎症被认为在慢性疼痛的产生中起关键作用。大量试验已证明促炎细胞因子在与外周和中枢伤害感受相关的疼痛病理生理学中的作用。促炎细胞因子的局部和全身表达被认为是疼痛的介质。在这些细胞因子中,肿瘤坏死因子-α(TNF-α)、白细胞介素-1β(IL-1β)和白细胞介素-6(IL-6)因其在神经损伤后的痛觉过敏作用而尤为显著。
本研究旨在评估和比较急性和慢性期退变椎间盘的韧带下型和游离碎片型中IL-1β、IL-6、白细胞介素-10(IL-10)和TNF-α的组织水平。
这是一项横断面研究。
对49例平均年龄为38.2±4.9岁、通过显微椎间盘切除术进行手术治疗的患者(24名女性,25名男性)进行了横断面研究。
在这些病例中,19例主诉时间少于6个月,而30例患者下腰痛和腿痛超过6个月。38例患者被诊断为韧带下型椎间盘退变,11例患者为游离碎片型椎间盘退变。
在显微椎间盘切除术中获取的髓核组织制备的组织样本中评估IL-1β、IL-6、IL-10和TNF-α的水平。将结果在主诉急性和慢性病程的患者以及韧带下型和游离碎片型椎间盘退变患者中进行比较。
主诉急性病程的患者中,IL-1β(p<0.001)、IL-6(p<0.001)、IL-10(p<0.001)和TNF-α(p<0.001)水平显著更高。同样,与韧带下型相比,游离碎片型椎间盘退变的IL-1β(p = 0.009)、IL-6(p<0.001)、IL-10(p = 0.024)和TNF-α(p = 0.017)水平明显更高。
炎性细胞因子似乎在椎间盘退变中尤其是在急性期和游离碎片型中起更明显的作用。应进行进一步试验以阐明分子水平的病理生理学并开发更有效的诊断和治疗措施。