Volume 30, Issue 4 pp. 463-469
Main Articles

The use of statistical MUNE in a multicenter clinical trial

J. M. Shefner MD, PhD

Corresponding Author

J. M. Shefner MD, PhD

Department of Neurology, SUNY Upstate Medical University, 750 East Adams Street, Syracuse, New York 13210, USA

Department of Neurology, SUNY Upstate Medical University, 750 East Adams Street, Syracuse, New York 13210, USASearch for more papers by this author
M. E. Cudkowicz MD

M. E. Cudkowicz MD

Neurology Clinical Trials Unit and Department of Neurology, Massachusetts General Hospital, Boston, Massachusetts, USA

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H. Zhang MA

H. Zhang MA

Biostatistics Center, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA

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D. Schoenfeld PhD

D. Schoenfeld PhD

Department of Neurology, SUNY Upstate Medical University, 750 East Adams Street, Syracuse, New York 13210, USA

Neurology Clinical Trials Unit and Department of Neurology, Massachusetts General Hospital, Boston, Massachusetts, USA

Biostatistics Center, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA

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D. Jillapalli MD

D. Jillapalli MD

Department of Neurology, SUNY Upstate Medical University, 750 East Adams Street, Syracuse, New York 13210, USA

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the Northeast ALS Consortium

the Northeast ALS Consortium

Participating members are listed at the end of this article.

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First published: 15 September 2004
Citations: 91

Abstract

Techniques to estimate motor unit number (MUNE) measure the number of functioning motor units in a muscle. In diseases characterized by progressive motor unit loss, such as amyotrophic lateral sclerosis (ALS), MUNE may be useful to monitor disease progression or beneficial response to treatment. As part of a multicenter, placebo-controlled, randomized, double-blind clinical trial testing the efficacy of creatine in patients with ALS, statistical MUNE was measured in 104 patients tested monthly for 6 months. The objective was to determine whether MUNE was a reliable and sensitive outcome measure in the context of a multicenter trial. Formal training and reliability testing was required for all MUNE evaluators. Testing of normal controls showed a high degree of test–retest reliability. All patient data were combined as the experimental treatment showed no efficacy. There was a 23% decline in MUNE over 6 months. The technique as employed in this trial overemphasized the presence of small motor units; this problem was partially addressed by poststudy data monitoring and censuring. Thus, MUNE can be used reliably as an outcome measure in multicenter clinical trials; specific remedies are suggested for the difficulties encountered in this study. Muscle Nerve 30: 463–469, 2004

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