Template-operated MUP analysis is not accurate in the diagnosis of myopathic or neuropathic changes in the diaphragm

被引:4
作者
Leonardis, Lea [1 ]
Podnar, Simon [1 ]
机构
[1] Univ Med Ctr Ljubljana, Inst Clin Neurophysiol, Div Neurol, 7 Zaloska Cesta, SI-1525 Ljubljana, Slovenia
来源
NEUROPHYSIOLOGIE CLINIQUE-CLINICAL NEUROPHYSIOLOGY | 2017年 / 47卷 / 5-6期
关键词
Amyotrophic lateral sclerosis; Diaphragm; Motor unit potentials; Myotonic dystrophy; Pulmonary function; AMYOTROPHIC-LATERAL-SCLEROSIS; PHRENIC-NERVE CONDUCTION; MYOTONIC-DYSTROPHY TYPE-2; INCLUSION-BODY MYOSITIS; UNIT POTENTIAL ANALYSIS; RESPIRATORY INSUFFICIENCY; MUSCULAR-DYSTROPHY; SPHINCTER ELECTROMYOGRAPHY; NEEDLE ELECTROMYOGRAPHY; PERIPHERAL NEUROPATHY;
D O I
10.1016/j.neucli.2017.07.003
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objectives. - The aim of this study was to evaluate the quantitative motor unit potential (MUP) analysis in the diagnosis of myopathy and neuropathy of the diaphragm. Methods. - Diaphragm template-operated quantitative EMG were performed in 30 patients with myotonic dystrophy type 1 (DM1), 17 with myotonic dystrophy type 2 (DM2) and 40 with amyotrophic lateral sclerosis (ALS). Results. - Low MUP amplitude precluded MUP analysis in 21% of DM1 patients. Only a single DM1 patient had EMG findings consistent with myopathy. In this patient, and another 4 DM1 and 3 DM2 patients, findings were consistent with neuropathy. Neuropathic MUP changes were found in 92% of ALS patients, but due to motor neuron cell loss in only 60% MUPs analyses could be done. Phrenic nerve conduction studies correlated with respiratory function tests, whereas MUP parameters did not. Conclusion. - Quantitative MUP analysis was not able to adequately sample diaphragm MUPs in patients with chronic myopathy or motor neuronopathy. (C) 2017 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:405 / 412
页数:8
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