Quantification of Fas protein in CSF of patients with neurocysticercosis

Arquivos de Neuro-Psiquiatria

José Augusto Camargo¹  Paulo Henrique Ferreira Bertolucci¹ 

[1],Universidade Federal de São Paulo Hospital São Paulo Departamento de Neurologia e NeurocirurgiaSão Paulo SP ,Brazil

关键词: neurocysticercosis;    Fas ligand protein;    cerebrospinal fluid;    neuronal damage;    neurocisticercose;    proteína ligante Fas;    líquido cefalorraquidiano;    dano neuronal;   

DOI  :  10.1590/S0004-282X2012000400007

来源: SciELO

【 摘 要 】

Neurocysticercosis is a parasitic disease that affects the central nervous system. The objective of this study was to investigate the correlation between neuronal death evaluated by the quantification of Fas apoptotic factor and the different evolutive forms of neurocysticercosis accompanied or not by epileptic seizures. METHODS: Cerebrospinal fluid samples from 36 patients with a diagnosis of neurocysticercosis divided into the following groups: active cystic form (n=15), 9 patients with and 6 without seizures, and calcified form (=21), 9 with and 12 without seizures. Fourteen patients comprised the control group. Fas protein concentrations were determined by ELISA. RESULTS: Only the group of patients with calcified cysts without seizures presented cerebrospinal fluid levels of Fas similar to those of the control group. Higher levels were observed for the other groups. CONCLUSIONS: The present finding suggests high cerebrospinal fluid levels of soluble Fas protein, except for patients with calcified cysts without seizures. Significant differences were observed for the group with calcified cysts and seizures, suggesting greater neuronal damage in these patients. Replacement of the term inactive cyst with reactive inactive cyst is suggested.

【 授权许可】

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