Patients with spinal muscular atrophy use high percentages of trunk muscle capacity to perform seated tasks

Laura H C Peeters, Mariska M H P Janssen, Idsart Kingma, Jaap H van Dieën, Imelda J M de Groot

Research output: Contribution to JournalArticleAcademicpeer-review

278 Downloads (Pure)

Abstract

OBJECTIVE: To investigate trunk function during seated upper extremity tasks in patients with spinal muscular atrophy (SMA) type 2 and 3.

DESIGN: 17 persons with SMA and 15 healthy controls (HC) performed several tasks when sitting unsupported, such as reaching (and placing) forward and sideward. Joint torque and muscle activity were measured during maximum voluntary isometric contractions (MVIC). Three-dimensional kinematics and normalized muscle activity were analyzed when performing tasks.

RESULTS: Trunk joint torques were significantly decreased, approximately 45%, in patients with SMA compared to HC. Active range of trunk motion was also significantly decreased in all directions. When performing tasks, the average back muscle activity was 27% and 56% of MVIC for respectively HC and SMA, and for abdominal muscles respectively 10% and 44% of MVIC. Trunk range of motion did not differ when performing daily tasks.

CONCLUSION: The trunk of patients with SMA is weaker compared to HC, reflected by reduced trunk torques and decreased active range of motion. Additionally, patients with SMA use high percentages of their trunk muscle capacity to perform tasks. Clinicians should take this into account for intervention development, because using high percentages of the maximum muscle capacity results in fatigue and muscle overloading.

Original languageEnglish
Pages (from-to)1110-1117
Number of pages8
JournalAmerican Journal of Physical Medicine and Rehabilitation
Volume98
Issue number12
Early online date2 Jul 2019
DOIs
Publication statusPublished - Dec 2019

Funding

This work was supported by the Netherlands Organisation for Scientific Research (Grant Numbers 13524 and 13525), Duchenne Parent Project, Stichting FSHD, Foundation to Eradicate Duchenne, Parent Project: Muscular Dystrophy, Focal Meditech, BAAT Medical, Summit Revalidatietechniek, Hankamp Rehab, Intespring, and Yumen Bionics.

FundersFunder number
Stichting FSHD
Yumen Bionics
Nederlandse Organisatie voor Wetenschappelijk Onderzoek13525, 13524
Duchenne Parent Project
Muskelsvindfonden

    Fingerprint

    Dive into the research topics of 'Patients with spinal muscular atrophy use high percentages of trunk muscle capacity to perform seated tasks'. Together they form a unique fingerprint.

    Cite this