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Photobiomodulation and visual stimulation against cognitive decline and Alzheimer's disease pathology: A systematic review

Publisher

WILEY
DOI: 10.1002/trc2.12249

Keywords

Alzheimer's disease; cognitive decline; light-based therapies; photobiomodulation; visual stimulation

Funding

  1. FCT (Fundacao para a Ciencia e Tecnologia) [SFRH/BD/09375/2020]
  2. FCT national funds [UIDB/04436/2020, UIDP/04436/2020]
  3. Northern Portugal Regional Operational Programme (NORTE 2020), under the Portugal 2020 Partnership Agreement, through the European Regional Development Fund (FEDER) [PTDC/EME-EME/1681/2021 - BrainStimMap, NORTE-01-0145-FEDER-000023]
  4. Foundation for Science and Technology (FCT) [UIDB/50026/2020, UIDP/50026/2020]
  5. Project Estrategico
  6. FCT [PEst-C/SAU/LA0026/2013]
  7. European Regional Development Fund COMPETE by Norte Portugal Regional Operational Programme (NORTE 2020) [FCOMP-01-0124-FEDER-037298, POCI-01-0145-FEDER-007038]
  8. [NORTE-01-0145-FEDER-000013]

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Light-based therapeutic modalities such as photobiomodulation (PBM) and visual stimulation (VS) show promise in attenuating Alzheimer's disease neuropathology and improving cognitive performance in both animal models and human studies. Further clinical investigation is needed to clarify their beneficial impact on AD patients.
IntroductionGiven the ineffectiveness of the available drug treatment against Alzheimer disease (AD), light-based therapeutic modalities have been increasingly receiving attention with photobiomodulation (PBM) and, more recently, visual stimulation (VS) being among the most promising approaches. However, the PBM and VS light parameters tested so far, as well as their outcomes, vary a lot with conflicting results being reported. MethodsBased on Scopus, PubMed, and Web of Science databases search, this systematic review summarizes, compares, and discusses 43 cell, animal, and human studies of PBM and VS related to cognitive decline and AD pathology. ResultsPreclinical work suggests that PBM with 640 +/- 30-nm light and VS at 40 Hz attenuates A beta and Tau pathology and improves neuronal and synaptic plasticity with most studies pointing towards enhancement of degradation/clearance mechanisms in the brain of AD animal models. Despite the gap of the translational evidence for both modalities, the few human studies performed so far support the use of PBM at 810-870 nm light pulsing at 40 Hz for improving brain network connectivity and memory in older subjects and AD patients, while 40 Hz VS in humans seems to improve cognition; further clinical investigation is urgently required to clarify the beneficial impact of PBM and VS in AD patients. DiscussionThis review highlights PBM and VS as promising light-based therapeutic approaches against AD brain neuropathology and related cognitive decline, clarifying the most effective light parameters for further preclinical and clinical testing and use. HighlightsLight-based brain stimulation produces neural entrainment and reverts neuronal damageBrain PBM and VS attenuate AD neuropathologyPMB and VS are suggested to improve cognitive performance in AD patients and animal modelsLight stimulation represents a promising therapeutic strategy against neurodegeneration

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