Expression of neurotrophic factors in cerebrospinal fluid and plasma of children with viral and bacterial meningoencephalitis

被引:32
作者
Chiaretti, A
Antonelli, A
Piastra, M
Genovese, O
Polidori, G
Aloe, L
机构
[1] Catholic Univ, Sch Med, Paediat Intens Care Unit, Rome, Italy
[2] CNR, Inst Neurobiol, Rome, Italy
关键词
brain-derived neurotrophic factor; child; glial-derived neurotrophic factor; meningoencephalitis; nerve growth factor;
D O I
10.1080/08035250410031314
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Aim: To evaluate the expression of neurotrophic factors (nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), glial-derived neurotrophic factor (GDNF)) and their association with the clinical-radiological characteristics and outcome of children with viral and bacterial meningoencephalitis (ME). Methods: Prospective observational clinical study performed on 13 children with ME and 12 controls with non-inflammatory obstructive hydrocephalus. Neurotrophic factor levels in the cerebro-spinal fluid (CSF) and plasma were measured using an immunoenzymatic assay. Results: High levels of NGF and BDNF were demonstrated in all patients, while GDNF levels did not undergo significant variations. NGF expression in the CSF was higher in viral ME than in bacterial ME and was correlated with CSF cellularity (particularly mononuclear cells). BDNF expression in the CSF was higher in bacterial ME than in viral ME and was correlated with CSF cellularity and blood platelet count. No relationships were noted between CSF protein or serum C-reactive protein levels and the expression of neurotrophic factors. Regarding clinical and radiological features, elevated NGF/BDNF levels in the CSF correlated with higher incidence of seizures and prolonged comatose state and with specific radiological lesions. No correlation was found between NGF/BDNF levels and final outcome. Conclusions: The variations in neurotrophic factor levels may reflect an endogenous attempt at neuroprotection against biochemical and molecular changes during both viral and bacterial ME. The expression of these factors is likely to play a neuro-immunomodulatory or neurosurvival role in ME infections.
引用
收藏
页码:1178 / 1184
页数:7
相关论文
共 31 条
[1]  
Aronica E, 2001, ACTA NEUROPATHOL, V101, P383
[2]   Neuronal instability: implications for Rett's syndrome [J].
Azmitia, EC .
BRAIN & DEVELOPMENT, 2001, 23 :S1-S10
[3]   The GDNF family ligands and receptors - implications for neural development [J].
Baloh, RH ;
Enomoto, H ;
Johnson, EM ;
Milbrandt, J .
CURRENT OPINION IN NEUROBIOLOGY, 2000, 10 (01) :103-110
[4]   TROPHIC FACTORS AND NEURONAL SURVIVAL [J].
BARDE, YA .
NEURON, 1989, 2 (06) :1525-1534
[5]  
BRDE YA, 1994, PROG CLIN BIOL RES, V390, P1855
[6]   NT-3 AND BDNF PROTECT CNS NEURONS AGAINST METABOLIC EXCITOTOXIC INSULTS [J].
CHENG, B ;
MATTSON, MP .
BRAIN RESEARCH, 1994, 640 (1-2) :56-67
[7]   Correlation between neurotrophic factor expression and outcome of children with severe traumatic brain injury [J].
Chiaretti, A ;
Piastra, M ;
Polidori, G ;
Di Rocco, C ;
Caresta, E ;
Antonelli, A ;
Amendola, T ;
Aloe, L .
INTENSIVE CARE MEDICINE, 2003, 29 (08) :1329-1338
[8]  
Fujimura H, 2002, THROMB HAEMOSTASIS, V87, P728
[9]   Congenital central hypoventilation syndrome: a novel mutation of the RET gene in an isolated case [J].
Kanai, M ;
Numakura, C ;
Sasaki, A ;
Shirahata, E ;
Akaba, K ;
Hashimoto, M ;
Hasegawa, H ;
Shirasawa, S ;
Hayasaka, K .
TOHOKU JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 196 (04) :241-246
[10]   Treatment with genetically engineered fibroblasts producing NGF or BDNF can accelerate recovery from traumatic spinal cord injury in the adult rat [J].
Kim, DH ;
Gutin, PH ;
Noble, LJ ;
Nathan, D ;
Yu, JS ;
Nockels, RP .
NEUROREPORT, 1996, 7 (13) :2221-2225