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DOI 10.1016/j.clinph.2017.02.015

Медицинская библиотека · Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology · 2017

A muscle ultrasound score in the diagnosis of amyotrophic lateral sclerosis.

Tsuji Yukiko, Noto Yu-Ichi, Shiga Kensuke, Teramukai Satoshi, Nakagawa Masanori, Mizuno Toshiki

Оценочное исследованиеСтатьяПеревод в очереди

Аннотация

OBJECTIVE

The aims of this study are to elucidate the frequencies and distribution of fasciculations using muscle ultrasound in patients with amyotrophic lateral sclerosis (ALS) and those with other conditions mimicking ALS, and subsequently to develop a novel fasciculation score for the diagnosis of ALS.

METHODS

Ultrasound of 21 muscles was performed to detect fasciculations in 36 consecutive patients suspected of having ALS. We developed a fasciculation ultrasound score that indicated the number of muscles with fasciculations in statistically selected muscles.

RESULTS

A total of 525 muscles in 25 ALS patients and 231 in 11 non-ALS patients were analysed. Using relative operating characteristic and multivariate logistic regression analysis, we selected the trapezius, deltoid, biceps brachii, abductor pollicis brevis, abdominal, vastus lateralis, vastus medialis, biceps femoris, and gastrocnemius muscles for the fasciculation ultrasound score. The mean scores were higher in the ALS group than those in the non-ALS group (5.3±0.5vs. 0.3±0.7) (mean±SD); p<0.001.

CONCLUSIONS

Two or more of the fasciculation ultrasound scores showed high sensitivity and specificity in differentiating ALS patients from non-ALS patients.

SIGNIFICANCE: The fasciculation ultrasound score can be a simple and useful diagnostic marker of ALS.

Для цитирования: Tsuji Yukiko, Noto Yu-Ichi, Shiga Kensuke, Teramukai Satoshi, Nakagawa Masanori, Mizuno Toshiki. A muscle ultrasound score in the diagnosis of amyotrophic lateral sclerosis.. Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology. 2017. DOI: 10.1016/j.clinph.2017.02.015.

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