首页> 外文期刊>The journal of pain: official journal of the American Pain Society >Evidence for a Role of Nerve Injury in Painful Intervertebral Disc Degeneration: A Cross-Sectional Proteomic Analysis of Human Cerebrospinal Fluid
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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:神经损伤在痛苦椎间盘退化中的作用的证据:人脑脊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, although >30% of adults have DD, LBP only develops in a subset of individuals. To gain insight into the mechanisms underlying nonpainful versus painful DD, human cerebrospinal fluid (CSF) was examined using differential expression shotgun proteomic techniques comparing healthy control participants, subjects with nonpainful 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 (eg, cystatin C) regardless of pain status. In contrast, most differentially expressed proteins in DD-associated chronic LBP patients were linked to nerve injury (eg, hemopexin). Cystatin C and hemopexin were selected for further examination using enzyme-linked immunosorbent assay 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 shows 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:椎间盘退化(DD)是一些人的腰痛(LBP)的原因。但是,虽然> 30%的成年人具有DD,但LBP仅在个人的子集中开发。为了深入了解非耐疼痛DD的潜在机制,使用差异表达射击蛋白质组学技术对人类脑脊髓液(CSF)进行检查,比较健康对照参与者,具有非耐肽DD的受试者,以及针对脊柱融合手术的痛苦DD患者。检测到八十八个蛋白质,其中27个差异表达。与DD相关的蛋白质往往与炎症(例如胱抑素C)有关,无论疼痛状态如何。相比之下,DD相关慢性LBP患者中最差异表达的蛋白质与神经损伤(例如血红素素)有关。选择胱抑素C和血红素素,用于在较大的队列中使用酶联免疫吸附测定进行进一步检查。亚斯塔丁C与DD严重程度相关但没有疼痛或残疾,血红素与疼痛强度,物理残疾和DD严重程度相关。本研究表明,CSF可用于研究人类疼痛DD的潜在DD的机制,并表明虽然痛苦的DD与神经损伤有关,炎症本身不足以发展LBP。

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