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
. 2024 Oct 9;24(1):381.
doi: 10.1186/s12883-024-03857-z.

Improvements in clinical signs and symptoms of Parkinson's disease using photobiomodulation: a five-year follow-up

Affiliations

Improvements in clinical signs and symptoms of Parkinson's disease using photobiomodulation: a five-year follow-up

Ann Liebert et al. BMC Neurol. .

Abstract

Background: Parkinson's disease is a progressive neurodegenerative disease characterized by clinical motor signs and non-motor symptoms that severely impact quality of life. There is an urgent need for therapies that might slow, halt or even reverse the progression of existing symptoms or delay the onset of new symptoms. Photobiomodulation is a therapy that has shown potential to alleviate some symptoms of Parkinson's disease in animal studies and in small clinical trials.

Objective: To assess long-term effectiveness of photobiomodulation therapy in a cohort of Parkinson's disease individuals after five years of continuing therapy.

Methods: Eight participants of the initial 12 in a previously published study agreed to be reassessed after five years. Seven of these participants had continued home-based, self-applied photobiomodulation therapy three times per week for five years. One participant had discontinued treatment after one year. Participants were assessed for a range of clinical motor signs, including MDS-UPDRS-III, measures of mobility and balance. Cognition was assessed objectively, and quality of life and sleep quality were assessed using self-reported questionnaires. A Wilcoxon Signed Ranks test was used to evaluate change in outcome measures between baseline (before treatment) and after five years, with the alpha value set to 0.05.

Results: Of the seven participants who had continued photobiomodulation therapy, one had a preliminary diagnosis of multisystem atrophy and was excluded from the group analysis. For the remaining six participants, there was a significant improvement in walk speed, stride length, timed up-and-go tests, tests of dynamic balance, and cognition compared to baseline and nonsignificant improvements in all other measures, apart from MDS-UPDRS-III, which was unchanged and one measure of static balance (single leg stance, standing on the unaffected leg with eyes open) which declined. Five of six participants either improved or showed no decline in MDS-UPDRS-III score and most participants showed improvement or no decline in all other outcome measures. No adverse effects of the photobiomodulation therapy were reported.

Conclusions: This study provides a signal that photobiomodulation therapy might safely reduce important clinical motor signs and non-motor symptoms in some Parkinson's disease patients, with improvements maintained over several years. Home-based photobiomodulation therapy has the potential to complement standard therapies to manage symptoms and potentially delay Parkinson's symptom progression.

Trial registration: Australian New Zealand Clinical Trials Registry, registration number ACTRN12618000038291p, registered on 12/01/2018.

Keywords: Cognition; Mobility; Motor symptoms; Parkinson’s disease; Photobiomodulation; Sense of smell.

PubMed Disclaimer

Conflict of interest statement

AL and BB are co-founders, and shareholders in SYMBYX Pty Ltd, a med-tech company developing photobiomodulation treatments for neurological disorders. HK and ELL are shareholders in SYMBYX Pty Ltd.

Figures

Fig. 1
Fig. 1
Changes in outcome measures from one to five years:  A - grouped MDS-UPDRS-III change; B - individual changes in MDS-UPDRS-III; 1 C - walk speed over 6 m; D - step length over 6 m; E, C – static balance score;  F - timed up-and-go (TUG) test; G - TUG manual test;  H - TUG cognitive test; I - spiral drawing test;  J - step test standing on affected leg;  K - step test standing on unaffected leg;  L - Montreal cognitive assessment (MoCA); M - Parkinson’s disease questionnaire summary index (PDQSI);  N - Parkinson’s disease sleep scale (PDSS)
Fig. 2
Fig. 2
Individual participant changes in outcome measures over five years for MDS-UPDRS-III, percentage change in motor symptoms from baseline, combined static balance (CSB) score and cognition (Montreal Cognitive Assessment – MoCA). The shaded area in the MDS-UPDRS graph is the score if a normal PD trajectory were to be followed

References

    1. Ou Z, Pan J, Tang S, Duan D, Yu D, Nong H, et al. Global trends in the incidence, prevalence, and years lived with disability of Parkinson’s disease in 204 countries/territories from 1990 to 2019. Front Public Health. 2021;9:776847. - PMC - PubMed
    1. Grünewald A, Kumar KR, Sue CM. New insights into the complex role of mitochondria in Parkinson’s disease. Prog Neurobiol. 2019;177:73–93. - PubMed
    1. Seppi K, Ray Chaudhuri K, Coelho M, Fox SH, Katzenschlager R, Perez Lloret S, et al. Update on treatments for nonmotor symptoms of Parkinson’s disease—an evidence-based medicine review. Mov Disord. 2019;34(2):180–98. - PMC - PubMed
    1. Fox SH, Katzenschlager R, Lim SY, Barton B, de Bie RMA, Seppi K, et al. International Parkinson and movement disorder society evidence-based medicine review: update on treatments for the motor symptoms of Parkinson’s disease. Mov Disord. 2018;33(8):1248–66. - PubMed
    1. Lewis MM, Harkins E, Lee EY, Stetter C, Snyder B, Corson T, et al. Clinical progression of Parkinson’s Disease: insights from the NINDS Common Data Elements. J Parkinsons Dis. 2020;10(3):1075–85. - PMC - PubMed