Correlates of outcome and response to IVIg in 88 patients with multifocal motor neuropathy

被引:118
作者
Cats, E. A. [1 ]
van der Pol, W. -L. [1 ]
Piepers, S. [1 ]
Franssen, H. [1 ,2 ]
Jacobs, B. C. [3 ]
van den Berg-Vos, R. M. [4 ]
Kuks, J. B. [5 ]
van Doorn, P. A. [3 ]
van Engelen, B. G. [6 ]
Verschuuren, J. J. [7 ]
Wokke, J. H. [1 ]
Veldink, J. H. [1 ]
van den Berg, L. H. [1 ]
机构
[1] Univ Med Ctr Utrecht, Dept Neurol, Rudolf Magnus Inst Neurosci, NL-3584 CX Utrecht, Netherlands
[2] Univ Med Ctr Utrecht, Dept Clin Neurophysiol, NL-3584 CX Utrecht, Netherlands
[3] Erasmus MC, Dept Neurol, Rotterdam, Netherlands
[4] St Lucas Andreas Hosp, Dept Neurol, Amsterdam, Netherlands
[5] Univ Groningen, Univ Med Ctr Groningen, Dept Neurol, Groningen, Netherlands
[6] Radboud Univ Nijmegen Med Ctr, Dept Neurol, Nijmegen, Netherlands
[7] Leiden Univ, Dept Neurol, Med Ctr, Leiden, Netherlands
关键词
IMMUNE-MEDIATED POLYNEUROPATHIES; GRADUATED TUNING FORK; CONDUCTION BLOCK; IMMUNOGLOBULIN TREATMENT; INTRAVENOUS IMMUNOGLOBULINS; DOUBLE-BLIND; DISEASE; GANGLIOSIDE; ANTIBODIES; SEVERITY;
D O I
10.1212/WNL.0b013e3181f0738e
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: Identification and examination of all patients with multifocal motor neuropathy (MMN) in the Netherlands to document the clinical spectrum and response to IV immunoglobulin (IVIg) and to determine correlates of outcome. Methods: A national cross-sectional descriptive study was performed. Ninety-seven patients were identified; 88 participated. Logistic regression analysis was used to study determinants of outcome. Results: Age at onset was younger in men than in women (38 vs 45 years, p = 0.05). Onset of weakness was in distal arm (61%) or distal leg (34%), and occasionally in the upper arm (5%). Initial diagnosis was motor neuron disease in one-third of patients. Brisk, but not pathologic, reflexes in weakened muscles were found in 8%. Conduction blocks were most frequently detected in the ulnar (80%) and median (77%) nerves, but occasionally only between Erb and axilla (6%), or in the musculocutaneous nerve (1%). Ninety-four percent responded to IVIg therapy: nonresponders had longer disease duration before the first treatment (p = 0.03). Seventy-six percent received IVIg maintenance treatment at the time of this study (median duration 6 years; range 0-17): the median dose increased over the years from 12 to 17 g per week (p < 0.01). Independent determinants of more severe weakness and disability were axon loss (p < 0.001; p < 0.0001) and longer disease duration without IVIg (p = 0.03; p = 0.07). Conclusion: The results of this study may help aid recognition the clinical picture of MMN. Early IVIg treatment may help to postpone axonal degeneration and permanent deficits. Classification of evidence: This study provides Class IV evidence that IVIg improves muscle strength of patients with MMN and disability (defined as an increase of >= 1 Medical Research Council grade in at least 2 muscle groups without decrease in other muscle groups) in 94% (95% confidence interval, 86.8%-97.4%) of patients. Neurology (R) 2010;75:818-825
引用
收藏
页码:818 / 825
页数:8
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