Martin-Vaquero P, da Costa R C, Moore S A, Gross A C, Eubank T D
Department of Veterinary Clinical Sciences, College of Veterinary Medicine, The Ohio State University , Columbus, OH.
J Vet Intern Med. 2014 Jul-Aug;28(4):1268-74. doi: 10.1111/jvim.12388. Epub 2014 Jun 25.
Chronic inflammation is involved in the pathogenesis of human cervical spondylotic myelopathy and could also play a role in cervical spondylomyelopathy (CSM) in dogs.
HYPOTHESIS/OBJECTIVES: That cerebrospinal fluid (CSF) cytokine concentrations would differ between clinically normal (control) and CSM-affected Great Danes (GDs), with affected GDs showing higher levels of inflammatory cytokines, such as interleukin (IL)-6 and monocyte chemoattractant protein-1/chemokine ligand 2 (MCP-1/CCL2).
Client-owned GDs: 15 control, 15 CSM-affected.
Prospective study. Dogs underwent cervical vertebral column magnetic resonance imaging and collection of CSF from the cerebellomedullary cistern. Cytokine concentrations were measured using a commercially available canine multiplex immunoassay. Cytokine concentrations were compared between groups. Associations with the administration of anti-inflammatory medications, disease duration and severity, severity of spinal cord (SC) compression, and SC signal changes were investigated in affected GDs.
Affected GDs had significantly lower MCP-1/CCL2 (mean 138.03 pg/mL, 95% confidence interval [CI] = 114.85-161.20) than control GDs (212.89 pg/mL, 95% CI = 165.68-260.11, P = .028). In affected GDs, MCP-1/CCL2 concentrations correlated inversely with the severity of SC compression. There were no associations with administration of anti-inflammatory medications, disease duration, or disease severity. IL-6 concentrations were significantly higher (2.20 pg/mL, 95% CI = 1.92-2.47, P < .001) in GDs with SC signal changes.
Lower MCP-1/CCL2 in CSM-affected GDs might compromise clearance of axonal and myelin debris, delay axon regeneration, and affect recovery. Higher IL-6 in CSM-affected GDs with SC signal changes suggests more severe inflammation in this group.
慢性炎症参与人类脊髓型颈椎病的发病机制,在犬脊髓型颈椎病(CSM)中也可能起作用。
假设/目的:临床正常(对照)和患CSM的大丹犬(GD)脑脊液(CSF)细胞因子浓度会有所不同,患CSM的GD炎症细胞因子水平更高,如白细胞介素(IL)-6和单核细胞趋化蛋白-1/趋化因子配体2(MCP-1/CCL2)。
客户拥有的GD:15只对照,15只患CSM。
前瞻性研究。犬接受颈椎磁共振成像并从小脑延髓池采集CSF。使用市售犬多重免疫测定法测量细胞因子浓度。比较组间细胞因子浓度。在患CSM的GD中研究与抗炎药物使用、病程和严重程度、脊髓(SC)压迫严重程度以及SC信号变化的相关性。
患CSM的GD的MCP-1/CCL2显著低于对照GD(平均138.03 pg/mL,95%置信区间[CI]=114.85-161.20)(212.89 pg/mL,95%CI=165.68-260.11,P=.028)。在患CSM的GD中,MCP-1/CCL2浓度与SC压迫严重程度呈负相关。与抗炎药物使用、病程或疾病严重程度无关。有SC信号变化的GD中IL-6浓度显著更高(2.20 pg/mL,95%CI=1.92-2.47,P<.001)。
患CSM的GD中较低的MCP-1/CCL2可能会损害轴突和髓磷脂碎片的清除,延迟轴突再生,并影响恢复。有SC信号变化的患CSM的GD中较高的IL-6表明该组炎症更严重。