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Evidence for a role of nerve injury in painful intervertebral disc degeneration: A cross-sectional proteomic analysis of human cerebrospinal fluid

机译:神经损伤在疼痛性椎间盘退变中的作用证据:人脑脊髓液的横截面蛋白质组学分析

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摘要

Intervertebral disc degeneration (DD) is a cause of low back pain (LBP) in some individuals. However, while >30% of adults have DD, LBP only develops in a subset of individuals. To gain insight into the mechanisms underlying non-painful versus painful DD, human cerebrospinal fluid (CSF) was examined using differential expression shotgun proteomic techniques comparing healthy controls, subjects with non-painful DD, and patients with painful DD scheduled for spinal fusion surgery. Eighty-eight proteins were detected, 27 of which were differentially expressed. Proteins associated with DD tended to be related to inflammation (e.g. cystatin C) regardless of pain status. In contrast, most differentially expressed proteins in DD-associated chronic LBP patients were linked to nerve injury (e.g. hemopexin). Cystatin C and hemopexin were selected for further examination by ELISA in a larger cohort. While Cystatin C correlated with DD severity but not pain or disability, hemopexin correlated with pain intensity, physical disability and DD severity. This study demonstrates that CSF can be used to study mechanisms underlying painful DD in humans, and suggests that while painful DD is associated with nerve injury, inflammation itself is not sufficient to develop LBP.
机译:椎间盘退变(DD)是某些人下腰痛(LBP)的原因。但是,尽管有超过30%的成年人患有DD,但LBP仅在部分个体中发展。为了深入了解非疼痛与疼痛DD的潜在机制,我们使用差异表达shot弹枪蛋白质组学技术对人脑脊液(CSF)进行了比较,比较了健康对照,非疼痛DD受试者和计划进行脊柱融合手术的DD疼痛患者。检测到88种蛋白质,其中27种差异表达。无论疼痛状态如何,与DD相关的蛋白质都倾向于与炎症相关(例如胱抑素C)。相反,在DD相关的慢性LBP患者中,大多数差异表达的蛋白质与神经损伤(例如,血红素)有关。选择了胱抑素C和血红蛋白以通过ELISA在更大的队列中进一步检查。胱抑素C与DD的严重程度相关,但与疼痛或残疾无关,而血红素与疼痛强度,身体残疾和DD的严重程度相关。这项研究表明,脑脊液可用于研究人类疼痛性DD的潜在机制,并表明尽管疼痛性DD与神经损伤有关,但炎症本身不足以发展LBP。

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