Djuric Niek, Lafeber Geraldine, van Duinen Sjoerd G, Bernards Sandra, Peul Wilco C, Vleggeert-Lankamp Carmen L A
Department of Neurosurgery, Leiden University Medical Center, Albinusdreef 2, 2300, RC, Leiden, The Netherlands.
Department of Pathology, Leiden University Medical Center, Albinusdreef 2, 2300, RC, Leiden, The Netherlands.
BMC Neurol. 2021 Sep 29;21(1):379. doi: 10.1186/s12883-021-02377-4.
Evidence indicates that inflammatory processes are involved in radicular pain as well as in resorption of herniated disc tissue. Furthermore there are indications that the presence of vertebral end plate pathology (Modic changes; MC) is associated with a negative effect on inflammation. It is hypothesized that in patients with MC, the (possibly bacterial induced) inflammation will be accompanied by pro inflammatory cytokines that worsen the outcome, and that in patients without MC, the inflammation is accompanied by cytokines that induce a resorption process to accelerate recovery.
This prospective cohort study will include 160 lumbar and 160 cervical patients (total of 320), which are scheduled for surgery for either a lumbar or cervical herniated disc with ages between 18 and 75. The main and interaction effects of local bacterial infection (culture), inflammatory cells in disc material (immunohistology), MC (MRI), and blood biomarkers indicating inflammation or infection (blood sample evaluation) will be evaluated. Clinical parameters to be evaluated are leg pain on the 11 point NRS pain scale, Oswestry (lumbar spine) or Neck (cervical spine) Disability Index, Global Perceived Recovery, Womac Questionnaire, and medication status, at baseline, and after 6, 16, 26 and 52 weeks.
Gaining insight in the aetiology of pain and discomfort in radiculopathy caused by a herniated disc could lead to more effective management of patients. If the type of inflammatory cells shows to be of major influence on the rate of recovery, new immunomodulating treatment strategies can be developed to decrease the duration and intensity of symptoms. Moreover, identifying a beneficial inflammatory response in the disc through a biomarker in blood could lead to early identification of patients whose herniations will resorb spontaneously versus those that require surgery.
prospectively enrolled at trialregister.nl, ID: NL8464 .
有证据表明,炎症过程与神经根性疼痛以及椎间盘突出组织的吸收有关。此外,有迹象表明椎体终板病变(Modic改变;MC)的存在对炎症有负面影响。据推测,在患有MC的患者中,(可能由细菌引起的)炎症会伴有促炎细胞因子,从而使病情恶化;而在没有MC的患者中,炎症会伴有诱导吸收过程以加速恢复的细胞因子。
这项前瞻性队列研究将纳入160例腰椎和160例颈椎患者(共320例),这些患者计划接受腰椎或颈椎椎间盘突出症手术,年龄在18至75岁之间。将评估局部细菌感染(培养)、椎间盘材料中的炎症细胞(免疫组织学)、MC(磁共振成像)以及指示炎症或感染的血液生物标志物(血液样本评估)的主要和交互作用。在基线以及6、16、26和52周后,要评估的临床参数包括11点数字评定量表上的腿痛、Oswestry(腰椎)或颈部(颈椎)功能障碍指数、总体感知恢复情况、Womac问卷以及用药情况。
深入了解椎间盘突出症引起的神经根病中疼痛和不适的病因,可能会导致对患者更有效的管理。如果炎症细胞类型对恢复速度有重大影响,就可以制定新的免疫调节治疗策略来缩短症状持续时间并减轻症状强度。此外,通过血液中的生物标志物识别椎间盘中有益的炎症反应,可能会早期识别出椎间盘突出将自发吸收的患者与那些需要手术的患者。
在trialregister.nl上进行前瞻性注册,ID:NL8464 。