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Muscle & nerve · 2020

Walking activity in a large cohort of boys with Duchenne muscular dystrophy.

СтатьяПоддержка NIH: внешняя программаНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
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Lott Donovan J, Taivassalo Tanja, Senesac Claudia R, Willcocks Rebecca J, Harrington Ann M, Zilke Kirsten, Cunkle Hilary, Powers Catherine, Finanger Erika L, Rooney William D, Tennekoon Gihan I, Vandenborne Krista

Аннотация

INTRODUCTION: In this study we explored walking activity in a large cohort of boys with Duchenne muscular dystrophy (DMD).

METHODS: Step activity (monitored for 7 days), functional ability, and strength were quantified in ambulatory boys (5-12.9 years of age) with DMD and unaffected boys. Ambulatory status was determined 2 years later.

RESULTS: Two to 5 days of activity monitoring predicted weekly step activity (adjusted R2 = 0.80-0.95). Age comparisons revealed significant declines for step activity with increasing age, and relationships were found between step activity with both function and strength (P < .01). Our regression model predicted 36.5% of the variance in step activity. Those who were still ambulatory after 2 years demonstrated baseline step activity nearly double that of those who were no longer walking 2 years later (P < .01).

DISCUSSION: Step activity for DMD is related to and predictive of functional declines, which may be useful for clinical trials.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты