共 36 条
Electrophysiological features in patients and presymptomatic relatives with spinocerebellar ataxia type 2
被引:47
作者:
Perez, Luis Velazquez
[1
]
Cruz, Gilberto Sanchez
[1
]
Ochoa, Nalia Canales
[1
]
Labrada, Roberto Rodriguez
[1
]
Diaz, Julio Rodriguez
[1
]
Mederos, Luis Almaguer
[1
]
Mesa, Jose Laffita
[1
]
机构:
[1] Ctr Res & Rehabil Hereditary Ataxias Carlos J Fin, Holguin 80100, Cuba
关键词:
spinocerebellar ataxia type 2 (SCA2);
cuban ataxia;
electrophysiological disorders;
sensory axonopathy;
nerve conduction studies;
evoked potentials;
D O I:
10.1016/j.jns.2007.07.013
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Motor and sensitive nerve conduction studies, visual (VEP), brainstem auditory (BAEP) and somatosensory (SSEP) evoked potentials in 82 patients with spinocerebellar ataxia type 2 (SCA2), 62 presymptomatics relatives and 80 controls, correlating it with CAG repeat, disease duration and ataxia score were assessed. All the groups showed differences in the amplitude of sensory action potentials in median and sural nerves. Sural amplitude was negatively correlated with disease duration and ataxia score. Differences among patients and controls in the mean latency and conduction velocity of sensory action potentials were found. Abnormal morphology and replicability of SSEPs and BSAEPs were found in patients and presymptomatics. Moreover, consistent increase in latencies of P40 component of SSEPs, III and V peaks and I -III interpeak of BSAEPs was found in patients. A positive correlation was found between latency of III and V waves, I-III and III-V interpeak latencies of BSAEPs and disease duration. CAG repeat and electrophysiological markers assessed were not correlative. Electrophysiological alterations in the SCA2 appeared in presymptomatic stages. These alterations are consistent markers which could be used to evaluate the progression of the disease. (c) 2007 Elsevier B. V. All rights reserved.
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页码:158 / 164
页数:7
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