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Dietary Glycemic Load and Plasma Amyloid-β Biomarkers of Alzheimer’s Disease

Previous studies have highlighted links between a high-glycemic-load (GL) diet and Alzheimer’s disease in apolipoprotein E ε4 (APOE4) carriers. However, the impact of high-GL diet on plasma amyloid-β (Aβ), an Alzheimer’s disease hallmark that can be detected decades before clinical symptomatology, i...

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Autores principales: Gentreau, Mélissa, Raymond, Michel, Samieri, Cécilia, Chuy, Virginie, Féart, Catherine, Berticat, Claire, Artero, Sylvaine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9230608/
https://www.ncbi.nlm.nih.gov/pubmed/35745215
http://dx.doi.org/10.3390/nu14122485
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author Gentreau, Mélissa
Raymond, Michel
Samieri, Cécilia
Chuy, Virginie
Féart, Catherine
Berticat, Claire
Artero, Sylvaine
author_facet Gentreau, Mélissa
Raymond, Michel
Samieri, Cécilia
Chuy, Virginie
Féart, Catherine
Berticat, Claire
Artero, Sylvaine
author_sort Gentreau, Mélissa
collection PubMed
description Previous studies have highlighted links between a high-glycemic-load (GL) diet and Alzheimer’s disease in apolipoprotein E ε4 (APOE4) carriers. However, the impact of high-GL diet on plasma amyloid-β (Aβ), an Alzheimer’s disease hallmark that can be detected decades before clinical symptomatology, is unknown. This study examined the association between plasma Aβ peptides (Aβ(40), Aβ(42) concentration and Aβ(42)/Aβ(40) ratio) and GL. The influence of the GL of four meal types (breakfast, lunch, afternoon snack, and dinner) was also determined. From the prospective Three-City study, 377 participants with plasma Aβ measurements, and who completed the Food Frequency Questionnaire, were selected. The association between plasma Aβ and GL was tested using an adjusted linear regression model. Lunch GL was associated with a lower plasma Aβ(42) concentration (β = −2.2 [CI = −4.27, −0.12], p = 0.038) and lower Aβ(42)/Aβ(40) ratio (β = −0.009 [CI = −0.0172, −0.0007], p = 0.034) in the model adjusted for center, age, sex, education level, APOE4 status, energy intake, serum creatinine, total cholesterol, and Mediterranean-like diet. No significant association was found with the GL of the other meal types. These results suggest that dietary GL may independently modulate the plasma Aβ of the APOE4 status. The mechanism underlying diet, metabolic response, and Aβ peptide regulation must be elucidated.
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spelling pubmed-92306082022-06-25 Dietary Glycemic Load and Plasma Amyloid-β Biomarkers of Alzheimer’s Disease Gentreau, Mélissa Raymond, Michel Samieri, Cécilia Chuy, Virginie Féart, Catherine Berticat, Claire Artero, Sylvaine Nutrients Article Previous studies have highlighted links between a high-glycemic-load (GL) diet and Alzheimer’s disease in apolipoprotein E ε4 (APOE4) carriers. However, the impact of high-GL diet on plasma amyloid-β (Aβ), an Alzheimer’s disease hallmark that can be detected decades before clinical symptomatology, is unknown. This study examined the association between plasma Aβ peptides (Aβ(40), Aβ(42) concentration and Aβ(42)/Aβ(40) ratio) and GL. The influence of the GL of four meal types (breakfast, lunch, afternoon snack, and dinner) was also determined. From the prospective Three-City study, 377 participants with plasma Aβ measurements, and who completed the Food Frequency Questionnaire, were selected. The association between plasma Aβ and GL was tested using an adjusted linear regression model. Lunch GL was associated with a lower plasma Aβ(42) concentration (β = −2.2 [CI = −4.27, −0.12], p = 0.038) and lower Aβ(42)/Aβ(40) ratio (β = −0.009 [CI = −0.0172, −0.0007], p = 0.034) in the model adjusted for center, age, sex, education level, APOE4 status, energy intake, serum creatinine, total cholesterol, and Mediterranean-like diet. No significant association was found with the GL of the other meal types. These results suggest that dietary GL may independently modulate the plasma Aβ of the APOE4 status. The mechanism underlying diet, metabolic response, and Aβ peptide regulation must be elucidated. MDPI 2022-06-15 /pmc/articles/PMC9230608/ /pubmed/35745215 http://dx.doi.org/10.3390/nu14122485 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Gentreau, Mélissa
Raymond, Michel
Samieri, Cécilia
Chuy, Virginie
Féart, Catherine
Berticat, Claire
Artero, Sylvaine
Dietary Glycemic Load and Plasma Amyloid-β Biomarkers of Alzheimer’s Disease
title Dietary Glycemic Load and Plasma Amyloid-β Biomarkers of Alzheimer’s Disease
title_full Dietary Glycemic Load and Plasma Amyloid-β Biomarkers of Alzheimer’s Disease
title_fullStr Dietary Glycemic Load and Plasma Amyloid-β Biomarkers of Alzheimer’s Disease
title_full_unstemmed Dietary Glycemic Load and Plasma Amyloid-β Biomarkers of Alzheimer’s Disease
title_short Dietary Glycemic Load and Plasma Amyloid-β Biomarkers of Alzheimer’s Disease
title_sort dietary glycemic load and plasma amyloid-β biomarkers of alzheimer’s disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9230608/
https://www.ncbi.nlm.nih.gov/pubmed/35745215
http://dx.doi.org/10.3390/nu14122485
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