Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2020 Aug 13:11:853.
doi: 10.3389/fneur.2020.00853. eCollection 2020.

Can Therapeutic Exercise Slow Down Progressive Functional Decline in Patients With Amyotrophic Lateral Sclerosis? A Meta-Analysis

Affiliations
Review

Can Therapeutic Exercise Slow Down Progressive Functional Decline in Patients With Amyotrophic Lateral Sclerosis? A Meta-Analysis

Donghwi Park et al. Front Neurol. .

Abstract

Background: Despite the high incidence of muscle weakness in patients with amyotrophic lateral sclerosis (ALS), the effects of therapeutic exercise on these individuals have not been clearly determined. Methods: A comprehensive database search was conducted on PubMed, Embase, Cochrane Library, and SCOPUS. We included studies published up to December 31, 2019 that fulfilled our inclusion and exclusion criteria. Functional status was determined as the Amyotrophic Lateral Sclerosis Functional Rating Scale (ALSFRS) score (previous and revised versions) before and after a therapeutic exercise program for the meta-analysis. The Cochrane Collaboration's tool for assessing risk of bias in randomized trials was used for the methodological quality assessments of included studies. The meta-analysis was performed using the RevMan v.5.3. Results: A total of 94 patients in the experimental group (who received therapeutic exercise) and 159 patients in the control group (who received conventional exercise or therapy) were included from five randomized controlled trials. The decrement of ALSFRS (previous version), ALSFRS-R (revised version), and ALSFRS-R-Respiratory scores at the 6-month evaluation were less for the therapeutic exercise group as compared to the control group. However, at the 6-month evaluation, the ALSFRS-R-Limb scores did not significantly differ between the two groups. Conclusions: Therapeutic exercise appears beneficial for patients with ALS. Further, it appears to exert more of a cardiopulmonary benefit, as opposed to preventing the progression of limb weakness. However, as the therapeutic exercises applied in each included study were not uniform, the result of our meta-analysis should be considered cautiously.

Keywords: amyotrophic lateral sclerosis; conventional exercise; meta-analysis; motor function; respiratory function; therapeutic exercise.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Flow diagram of study selection.
Figure 2
Figure 2
Quality assessment for selected studies.
Figure 3
Figure 3
Forest plot of 6-month outcomes. (A) Amyotrophic lateral sclerosis functional rating scale (ALSFRS)-Total, (B) ALSFRS-R-Total, (C) ALSFRS-R-Respiratory, (D) ALSFRS-R-Limb.
Figure 4
Figure 4
Graphic funnel plot of three studies [Braga et al. (24), Kitano et al. (20), and Zucchi et al.'s (25) studies] depicting differences of 6-month amyotrophic lateral sclerosis functional rating scale (ALSFRS)-Total score.

Similar articles

Cited by

References

    1. Kiernan MC, Vucic S, Cheah BC, Turner MR, Eisen A, Hardiman O, et al. . Amyotrophic lateral sclerosis. Lancet. (2011) 377:942–55. 10.1016/S0140-6736(10)61156-7 - DOI - PubMed
    1. Renton AE, Chio A, Traynor BJ. State of play in amyotrophic lateral sclerosis genetics. Nat Neurosci. (2014) 17:17–23. 10.1038/nn.3584 - DOI - PMC - PubMed
    1. Visser J, van den Berg-Vos RM, Franssen H, van den Berg LH, Wokke JH, de Jong JM, et al. . Disease course and prognostic factors of progressive muscular atrophy. Arch Neurol. (2007) 64:522–8. 10.1001/archneur.64.4.522 - DOI - PubMed
    1. Park JS, Do YW, Park JM, Seok HY, Park D. Under-recognized primary spontaneous pneumothorax in ALS: a multicenter retrospective study. Neurol Sci. (2019) 40:2509–14. 10.1007/s10072-019-03989-y - DOI - PubMed
    1. Park JS, Park D. The terminal latency of the phrenic nerve correlates with respiratory symptoms in amyotrophic lateral sclerosis. Clin Neurophysiol. (2017) 128:1625–8. 10.1016/j.clinph.2017.06.039 - DOI - PubMed