Serum time course of two brain-specific proteins, α1 brain globulin and neuron-specific enolase, in tick-born encephalitis and Lyme disease

被引:10
作者
Chekhonin, VP [1 ]
Zhirkov, YA [1 ]
Belyaeva, IA [1 ]
Ryabukhin, IA [1 ]
Gurina, OI [1 ]
Dmitriyeva, TB [1 ]
机构
[1] Serbsky Natl Res Ctr Social & Forens Psychiat, Lab Immunochem, Moscow 119839, Russia
关键词
tick-born encephalitis; Lyme neuroborreliosis; alpha(1) brain globulin; NSE; elimination rate constants;
D O I
10.1016/S0009-8981(02)00057-8
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
Methods: Time courses of the serum concentrations of two brain-specific proteins (BSP), alpha(1) brain globulin (alpha(1)BG, an astroglial marker) and neuron-specific enolase (NSE), were studied in patients with severe tick-born encephalitis (TBE) and Lyme disease (LD; neuroborreliosis). The concentrations were determined on the second day of the acute phase and then on the 7th, 12th, 18th, and 23rd days. Apparent rate constants for the elimination of the BSP from blood (k(e)) were calculated with the non-linear regression. Results: In patients with TBE, the highest serum concentrations of alpha(1)BG and NSE, observed on the second day, were followed by their monotonic decrease to the normal levels reached by the 23rd day. The mean k(c) values for alpha(1)BG and NSE were found to be significantly different (0.086+/-0.003 vs. 0.057+/-0.006 day(-1) respectively; p<0.05). Higher serum levels of both BSP were observed in the more severe clinical cases and in the cases with unfavorable outcomes. Similar profiles were also observed for the serum α(1)BG and NSE in LD. Conclusions: These results suggest that, in the patients examined, the blood-brain barrier was partially impaired; the quantitative parameters of the serum BSP time courses can be indicative of the extents of the neuronal and/or glial lesions. (C) 2002 Published by Elsevier Science B.V.
引用
收藏
页码:117 / 125
页数:9
相关论文
共 19 条
[1]  
BELYAEVA IA, 1995, THESIS RUSS ST MED U
[2]  
BELYAEVA IA, 1995, RUSS J NEUROPATHOL P, V6, P25
[3]   NEURON-SPECIFIC ENOLASE IN CEREBROSPINAL-FLUID - A BIOCHEMICAL MARKER FOR NEURONAL DEGENERATION IN DEMENTIA DISORDERS [J].
BLENNOW, K ;
WALLIN, A ;
EKMAN, R .
JOURNAL OF NEURAL TRANSMISSION-PARKINSONS DISEASE AND DEMENTIA SECTION, 1994, 8 (03) :183-191
[4]   Glial fibrillary acidic protein is increased in the cerebrospinal fluid of preterm infants with abnormal neurological findings [J].
Blennow, M ;
Rosengren, L ;
Jonsson, S ;
Forssberg, H ;
KatzSalamon, M ;
Hagberg, H ;
Hesser, U ;
Lagercrantz, H .
ACTA PAEDIATRICA, 1996, 85 (04) :485-489
[5]  
CHEKHONIN VP, 2002, UNPUB IMMUNOCHEMICAL
[6]  
DORENKO EP, 1989, THESIS RUSS ST MED U
[7]   Increased cerebrospinal fluid levels of glial fibrillary acidic protein (GFAp) in lyme neuroborreliosis [J].
Dotevall, L ;
Rosengren, LE ;
Hagberg, L .
INFECTION, 1996, 24 (02) :125-129
[8]   Astroglial and neuronal proteins in cerebrospinal fluid as markers of CNS involvement in Lyme neuroborreliosis [J].
Dotevall, L ;
Hagberg, T ;
Karlsson, JE ;
Rosengren, LE .
EUROPEAN JOURNAL OF NEUROLOGY, 1999, 6 (02) :169-178
[9]  
Hansen K, 1994, Acta Neurol Scand Suppl, V151, P1
[10]   Release of biochemical markers of damage to neuronal and glial brain tissue is associated with short and long term neuropsychological outcome after traumatic brain injury [J].
Herrmann, M ;
Curio, N ;
Jost, S ;
Grubich, C ;
Ebert, AD ;
Fork, ML ;
Synowitz, H .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2001, 70 (01) :95-100