Analyses of transthyretin concentration in the cerebrospinal fluid of patients with Guillain-Barre syndrome and other neurological disorders

被引:19
作者
Chiang, Han-Lin [1 ]
Lyu, Rong-Kuo [1 ]
Tseng, Mu-Yun [1 ]
Chang, Kuo-Hsuan [1 ]
Chang, Hong-Shiu [1 ]
Hsu, Wen-Chuin [1 ]
Kuo, Hung-Chou [1 ]
Chu, Chun-Che [1 ]
Wu, Yih-Ru [1 ]
Ro, Long-Sun [1 ]
Huang, Chin-Chang [1 ]
Chen, Chiung-Mei [1 ]
机构
[1] Chang Gung Univ, Chang Gung Mem Hosp, Coll Med, Dept Neurol, Taipei, Taiwan
关键词
Transthyretin; Cerebrospinal fluid; Guillain-Barre syndrome; INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY; TRAUMATIC BRAIN-INJURY; MULTIPLE-SCLEROSIS; ALZHEIMERS-DISEASE; PRE-ALBUMIN; IDIOPATHIC POLYNEURITIS; COMPARATIVE PROTEOMICS; DIAGNOSTIC-CRITERIA; APOLIPOPROTEIN-E; PROTEIN MARKERS;
D O I
10.1016/j.cca.2009.04.022
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: Guillain-Barre syndrome (GBS) is an autoimmune inflammatory polyradiculoneuropathy that causes acute are flexic paralysis with a high risk of respiratory failure. Previously, using two-dimensional gel electrophoresis and mass spectrometry, we found that the transthyretin level was altered in the cerebrospinal fluid (CSF) of GBS patients when compared to that in CSF of control patients. Methods: We used enzyme-linked immunosorbent assay (ELISA) to measure the transthyretin levels in the CSF and serum from 22 GBS, 4 Miller-Fisher syndrome (MFS), 9 chronic inflammatory demyelinating polyradiculoneuropathy (CIDP), 22 multiple sclerosis (MS), 10 Alzheimer's disease (AD), and 6 viral meningitis (VM) patients, and 18 controls. Results: The results show that CSF transthyretin concentration of the GBS patients is significantly higher than that of the control, MS, AD and VM patients (p < 0.05), although not significantly different from that of MFS and CIDP patients. Conclusion: The increased CSF transthyretin level may be explained by barrier dysfunction or decreased CSF flow in the GBS patients along with increased intrathecal synthesis of transthyretin that might be a protective response to nerve damage. (c) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:143 / 147
页数:5
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