Central motor conduction time in progressive multiple sclerosis - Correlations with MRI and disease activity

被引:46
作者
Kidd, D
Thompson, PD
Day, BL
Rothwell, JC
Kendall, BE
Thompson, AJ
Marsden, CD
McDonald, WI
机构
[1] UCL Natl Hosp Neurol & Neurosurg, Inst Neurol, NMR Res Unit, London WC1N 3BG, England
[2] UCL Natl Hosp Neurol & Neurosurg, Inst Neurol, MRC, Human Movement & Balance Unit, London WC1N 3BG, England
关键词
multiple sclerosis; motor conduction time; MRI; pathophysiology;
D O I
10.1093/brain/121.6.1109
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The purpose of this study was to relate abnormalities of motor conduction time to the presence of spinal cord MRI lesions:in progressive multiple sclerosis and to investigate the relationship between changes in motor conduction over time and clinical and MRI changes. Central motor conduction time (CMCT), serial MRI of the brain and spinal cord, and clinical evaluations were carried out in 20 patients with primary and secondary progressive multiple sclerosis, CMCT was carried out at the beginning and end of the study whilst the clinical and MRT examinations occurred at monthly intervals for 12 months. Median CMCT to abductor pollicis brevis was 14.8 ms (range 8.8-27.4 ms). The response latency to tibialis anterior correlated with disability measured on the Expanded Disability Status Scale. Latencies to upper limb muscles correlated with cervical MRI lesion load and the presence of atrophy of the cervical cord. Over the 12-month study period, 15 of 19 patients deteriorated clinically. However, an increase in motor response latencies occurred only in the four patients who had developed new cord lesions. The results suggest that prolonged CMCT is related to spinal cord lesion load and that, over time, changes in the CMCT occur only when spinal cord lesion load increases. Clinical change in progressive multiple sclerosis may therefore occur without either the development of new lesions on MRI scans or an increase in motor conduction time. This suggests that clinical deterioration in these patients may occur by a mechanism other than increasing demyelination. This may be progressive axonal degeneration.
引用
收藏
页码:1109 / 1116
页数:8
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