A pilot study of neuromuscular ultrasound as a biomarker for amyotrophic lateral sclerosis

被引:15
作者
Pathak, Sapna [1 ]
Caress, James B. [1 ]
Wosiski-Kuhn, Marlena [2 ]
Milligan, Carol [2 ]
Williams, Delaney [2 ]
Cartwright, Michael S. [1 ]
机构
[1] Wake Forest Sch Med, Dept Neurol, Winston Salem, NC 27101 USA
[2] Wake Forest Sch Med, Dept Neurobiol & Anat, Winston Salem, NC USA
关键词
amyotrophic lateral sclerosis; biomarker; correlation; muscle; reliability; ultrasound; QUANTITATIVE MUSCLE ULTRASONOGRAPHY; ALSFRS-R; RELIABILITY; PROGRESSION; DIAGNOSIS; VALIDITY; RATER;
D O I
10.1002/mus.26360
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: This study explores the reliability and responsiveness of neuromuscular ultrasound in amyotrophic lateral sclerosis (ALS). Methods: Investigations were conducted with 10 healthy controls, 10 patients with ALS (single point in time), and 10 different patients with ALS (followed over 6 months; 4 completed follow-up). Ultrasound was used to measure the thickness of the geniohyoid, bilateral biceps/brachialis, bilateral tibialis anterior, and bilateral hemidiaphragms (at inspiration and expiration). Interrater and intrarater reliability and change in muscle thickness over 6 months were measured. Results: Interrater correlation coefficients ranged between 0.80 and 0.99 in healthy controls and between 0.78 and 0.97 in patients with ALS. Intrarater correlation coefficients ranged between 0.83 and 0.98 in healthy controls. The mean percentage decline in muscle thickness over 6 months was 20.25%. Discussion: Muscle ultrasound appears to be a reliable technique for measuring important muscles in patients with ALS. Larger studies with age-matched controls should be conducted to assess further the responsiveness of this biomarker in ALS. Muscle Nerve 59:181-186, 2019
引用
收藏
页码:181 / 186
页数:6
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