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Nutritional ketosis for mild cognitive impairment in Parkinson's disease: A controlled pilot trial

INTRODUCTION: Glucose hypometabolism and insulin resistance increase risk for and accelerate progression in Parkinson's disease and neurocognitive disorders. We conducted a proof of concept trial to determine whether ketogenesis, a metabolic adaptation induced by dietary carbohydrate restrictio...

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Autores principales: Krikorian, Robert, Shidler, Marcelle D., Summer, Suzanne S., Sullivan, Patrick G., Duker, Andrew P., Isaacson, Richard S., Espay, Alberto J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8288565/
https://www.ncbi.nlm.nih.gov/pubmed/34316598
http://dx.doi.org/10.1016/j.prdoa.2019.07.006
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author Krikorian, Robert
Shidler, Marcelle D.
Summer, Suzanne S.
Sullivan, Patrick G.
Duker, Andrew P.
Isaacson, Richard S.
Espay, Alberto J.
author_facet Krikorian, Robert
Shidler, Marcelle D.
Summer, Suzanne S.
Sullivan, Patrick G.
Duker, Andrew P.
Isaacson, Richard S.
Espay, Alberto J.
author_sort Krikorian, Robert
collection PubMed
description INTRODUCTION: Glucose hypometabolism and insulin resistance increase risk for and accelerate progression in Parkinson's disease and neurocognitive disorders. We conducted a proof of concept trial to determine whether ketogenesis, a metabolic adaptation induced by dietary carbohydrate restriction, can improve cognitive performance in Parkinson's disease patients with mild cognitive impairment. METHODS: We enrolled patients with mild cognitive impairment associated with Parkinson's disease in an eight-week nutritional intervention with random assignment to either high-carbohydrate consumption typical of the Western dietary pattern (n = 7) or to a low-carbohydrate, ketogenic regimen (n = 7). We assessed changes in cognitive performance as well as motor function, anthropometrics, and metabolic parameters. RESULTS: Relative to the high-carbohydrate group, the low-carbohydrate group demonstrated improvements in lexical access (p = 0.02, Cohen's f effect size = 0.76) and memory (p = 0.01, f = 0.87) and as well as a trend for reduced interference in memory (p = 0.06, f = 0.60). The low-carbohydrate group also exhibited reduced body weight (p < 0.0001, f = 1.89) and increased circulation of beta-hydroxybutyrate (p = 0.01, f = 0.90). Change in body weight was strongly associated with memory performance (p = 0.001). Motor function was not affected by the intervention. CONCLUSION: Nutritional ketosis enhanced cognitive performance in Parkinson's disease-associated mild cognitive impairment in this pilot study. This metabolic intervention and its mechanisms deserve further investigation in the context of neurodegeneration.
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spelling pubmed-82885652021-07-26 Nutritional ketosis for mild cognitive impairment in Parkinson's disease: A controlled pilot trial Krikorian, Robert Shidler, Marcelle D. Summer, Suzanne S. Sullivan, Patrick G. Duker, Andrew P. Isaacson, Richard S. Espay, Alberto J. Clin Park Relat Disord Original Article INTRODUCTION: Glucose hypometabolism and insulin resistance increase risk for and accelerate progression in Parkinson's disease and neurocognitive disorders. We conducted a proof of concept trial to determine whether ketogenesis, a metabolic adaptation induced by dietary carbohydrate restriction, can improve cognitive performance in Parkinson's disease patients with mild cognitive impairment. METHODS: We enrolled patients with mild cognitive impairment associated with Parkinson's disease in an eight-week nutritional intervention with random assignment to either high-carbohydrate consumption typical of the Western dietary pattern (n = 7) or to a low-carbohydrate, ketogenic regimen (n = 7). We assessed changes in cognitive performance as well as motor function, anthropometrics, and metabolic parameters. RESULTS: Relative to the high-carbohydrate group, the low-carbohydrate group demonstrated improvements in lexical access (p = 0.02, Cohen's f effect size = 0.76) and memory (p = 0.01, f = 0.87) and as well as a trend for reduced interference in memory (p = 0.06, f = 0.60). The low-carbohydrate group also exhibited reduced body weight (p < 0.0001, f = 1.89) and increased circulation of beta-hydroxybutyrate (p = 0.01, f = 0.90). Change in body weight was strongly associated with memory performance (p = 0.001). Motor function was not affected by the intervention. CONCLUSION: Nutritional ketosis enhanced cognitive performance in Parkinson's disease-associated mild cognitive impairment in this pilot study. This metabolic intervention and its mechanisms deserve further investigation in the context of neurodegeneration. Elsevier 2019-08-06 /pmc/articles/PMC8288565/ /pubmed/34316598 http://dx.doi.org/10.1016/j.prdoa.2019.07.006 Text en © 2019 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Krikorian, Robert
Shidler, Marcelle D.
Summer, Suzanne S.
Sullivan, Patrick G.
Duker, Andrew P.
Isaacson, Richard S.
Espay, Alberto J.
Nutritional ketosis for mild cognitive impairment in Parkinson's disease: A controlled pilot trial
title Nutritional ketosis for mild cognitive impairment in Parkinson's disease: A controlled pilot trial
title_full Nutritional ketosis for mild cognitive impairment in Parkinson's disease: A controlled pilot trial
title_fullStr Nutritional ketosis for mild cognitive impairment in Parkinson's disease: A controlled pilot trial
title_full_unstemmed Nutritional ketosis for mild cognitive impairment in Parkinson's disease: A controlled pilot trial
title_short Nutritional ketosis for mild cognitive impairment in Parkinson's disease: A controlled pilot trial
title_sort nutritional ketosis for mild cognitive impairment in parkinson's disease: a controlled pilot trial
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8288565/
https://www.ncbi.nlm.nih.gov/pubmed/34316598
http://dx.doi.org/10.1016/j.prdoa.2019.07.006
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