A feasibility trial of gamma sensory flicker for patients with prodromal Alzheimer's disease

Introduction We and collaborators discovered that flickering lights and sound at gamma frequency (40 Hz) reduce Alzheimer's disease (AD) pathology and alter immune cells and signaling in mice. To determine the feasibility of this intervention in humans we tested the safety, tolerability, and da...

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Published in:Alzheimer's & dementia : translational research & clinical interventions Vol. 7; no. 1; pp. e12178 - n/a
Main Authors: He, Qiliang, Colon‐Motas, Kay M., Pybus, Alyssa F., Piendel, Lydia, Seppa, Jonna K., Walker, Margaret L., Manzanares, Cecelia M., Qiu, Deqiang, Miocinovic, Svjetlana, Wood, Levi B., Levey, Allan I., Lah, James J., Singer, Annabelle C.
Format: Journal Article
Language:English
Published: United States John Wiley & Sons, Inc 2021
John Wiley and Sons Inc
Wiley
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Summary:Introduction We and collaborators discovered that flickering lights and sound at gamma frequency (40 Hz) reduce Alzheimer's disease (AD) pathology and alter immune cells and signaling in mice. To determine the feasibility of this intervention in humans we tested the safety, tolerability, and daily adherence to extended audiovisual gamma flicker stimulation. Methods Ten patients with mild cognitive impairment due to underlying AD received 1‐hour daily gamma flicker using audiovisual stimulation for 4 or 8 weeks at home with a delayed start design. Results Gamma flicker was safe, tolerable, and adherable. Participants’ neural activity entrained to stimulation. Magnetic resonance imaging and cerebral spinal fluid proteomics show preliminary evidence that prolonged flicker affects neural networks and immune factors in the nervous system. Discussion These findings show that prolonged gamma sensory flicker is safe, tolerable, and feasible with preliminary indications of immune and network effects, supporting further study of gamma stimulation in AD.
Bibliography:James J. Lah and Annabelle C. Singer contributed equally to this study.
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ISSN:2352-8737
2352-8737
DOI:10.1002/trc2.12178