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脑脊液高迁移率族蛋白 B1 与视神经脊髓炎的鞘内炎症和星形胶质细胞损伤有关。

CSF high-mobility group box 1 is associated with intrathecal inflammation and astrocytic damage in neuromyelitis optica.

机构信息

Department of Neurology, Graduate School of Medicine, Chiba University, 1-8-1, Inohana, Chuo-ku, Chiba 260-8670, Japan.

出版信息

J Neurol Neurosurg Psychiatry. 2013 May;84(5):517-22. doi: 10.1136/jnnp-2012-304039. Epub 2012 Dec 19.

Abstract

OBJECTIVE

High-mobility group box 1 (HMGB1) acts as a proinflammatory mediator when released by cells. Recent studies implicate extracellular HMGB1 in the pathogenesis of various autoimmune diseases. Our main aim of this study is to determine whether HMGB1 is involved in the neuromyelitis optica (NMO) inflammatory process.

METHODS

Cerebrospinal fluid (CSF) and serum HMGB1 levels in 42 NMO patients were compared with those in 30 multiple sclerosis (MS) patients, and 30 patients with other noninflammatory neurological disorders (ONNDs). We also tested the possible correlation between CSF HMGB1 levels and the clinical and laboratory variables in NMO patients.

RESULTS

CSF HMGB1 levels in NMO patients were higher than those in MS and ONNDs patients (p<0.001), and these levels in MS patients were higher than those in ONNDs patients (p<0.001). After treatment, the CSF HMGB1 levels in NMO patients decreased to normal. In addition, CSF HMGB1 levels correlated with CSF cell counts, CSF protein levels, CSF interleukin-6 levels, CSF glial fibrillary acidic protein levels, and CSF/serum albumin ratio (p≤0.001). Serum HMGB1 levels in MS patients were significantly higher than those in ONNDs patients (p=0.002).

CONCLUSIONS

HMGB1 could play a key role in central nervous system inflammation in NMO patients.

摘要

目的

高迁移率族蛋白 B1(HMGB1)在细胞释放时充当促炎介质。最近的研究表明,细胞外 HMGB1 参与了各种自身免疫性疾病的发病机制。我们这项研究的主要目的是确定 HMGB1 是否参与视神经脊髓炎(NMO)炎症过程。

方法

比较了 42 名 NMO 患者、30 名多发性硬化症(MS)患者和 30 名其他非炎症性神经疾病(ONND)患者的脑脊液(CSF)和血清 HMGB1 水平。我们还测试了 NMO 患者 CSF HMGB1 水平与临床和实验室变量之间的可能相关性。

结果

NMO 患者的 CSF HMGB1 水平高于 MS 和 ONND 患者(p<0.001),MS 患者的 CSF HMGB1 水平高于 ONND 患者(p<0.001)。治疗后,NMO 患者的 CSF HMGB1 水平降至正常。此外,CSF HMGB1 水平与 CSF 细胞计数、CSF 蛋白水平、CSF 白细胞介素-6 水平、CSF 胶质纤维酸性蛋白水平和 CSF/血清白蛋白比值相关(p≤0.001)。MS 患者的血清 HMGB1 水平明显高于 ONND 患者(p=0.002)。

结论

HMGB1 可能在 NMO 患者的中枢神经系统炎症中发挥关键作用。

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