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Dietary magnesium intake is related to larger brain volumes and lower white matter lesions with notable sex differences

PURPOSE: To examine the association between dietary magnesium (Mg) intake and brain volumes and white matter lesions (WMLs) in middle to early old age. METHODS: Participants (aged 40–73 years) from UK Biobank (n = 6001) were included and stratified by sex. Dietary Mg was measured using an online com...

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Autores principales: Alateeq, Khawlah, Walsh, Erin I., Cherbuin, Nicolas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10349698/
https://www.ncbi.nlm.nih.gov/pubmed/36899275
http://dx.doi.org/10.1007/s00394-023-03123-x
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author Alateeq, Khawlah
Walsh, Erin I.
Cherbuin, Nicolas
author_facet Alateeq, Khawlah
Walsh, Erin I.
Cherbuin, Nicolas
author_sort Alateeq, Khawlah
collection PubMed
description PURPOSE: To examine the association between dietary magnesium (Mg) intake and brain volumes and white matter lesions (WMLs) in middle to early old age. METHODS: Participants (aged 40–73 years) from UK Biobank (n = 6001) were included and stratified by sex. Dietary Mg was measured using an online computerised 24 h recall questionnaire to estimate daily Mg intake. Latent class analysis and hierarchical linear regression models were performed to investigate the association between baseline dietary Mg, Mg trajectories, and brain volumes and WMLs. Associations between baseline Mg, and baseline blood pressure (BP) measures, and baseline Mg, Mg trajectories and BP changes (between baseline and wave 2) were also investigated to assess whether BP mediates the link between Mg intake and brain health. All analyses controlled for health and socio-demographic covariates. Possible interactions between menopausal status and Mg trajectories in predicting brain volumes and WMLs were also investigated. RESULTS: On average, higher baseline dietary Mg intake was associated with larger brain volumes (gray matter [GM]: 0.001% [SE = 0.0003]; left hippocampus [LHC]: 0.0013% [SE = 0.0006]; and right hippocampus [RHC]: 0.0023% [SE = 0.0006]) in both men and women. Latent class analysis of Mg intake revealed three classes: “high-decreasing” (men = 3.2%, women = 1.9%), “low-increasing” (men = 1.09%, women = 1.62%), and “stable normal” (men = 95.71%, women = 96.51%). In women, only the “high-decreasing” trajectory was significantly associated with larger brain volumes (GM: 1.17%, [SE = 0.58]; and RHC: 2.79% [SE = 1.11]) compared to the “normal-stable”, the “low-increasing” trajectory was associated with smaller brain volumes (GM: − 1.67%, [SE = 0.30]; white matter [WM]: − 0.85% [SE = 0.42]; LHC: − 2.43% [SE = 0.59]; and RHC: − 1.50% [SE = 0.57]) and larger WMLs (1.6% [SE = 0.53]). Associations between Mg and BP measures were mostly non-significant. Furthermore, the observed neuroprotective effect of higher dietary Mg intake in the “high-decreasing” trajectory appears to be greater in post-menopausal than pre-menopausal women. CONCLUSIONS: Higher dietary Mg intake is related to better brain health in the general population, and particularly in women. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00394-023-03123-x.
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spelling pubmed-103496982023-07-17 Dietary magnesium intake is related to larger brain volumes and lower white matter lesions with notable sex differences Alateeq, Khawlah Walsh, Erin I. Cherbuin, Nicolas Eur J Nutr Original Contribution PURPOSE: To examine the association between dietary magnesium (Mg) intake and brain volumes and white matter lesions (WMLs) in middle to early old age. METHODS: Participants (aged 40–73 years) from UK Biobank (n = 6001) were included and stratified by sex. Dietary Mg was measured using an online computerised 24 h recall questionnaire to estimate daily Mg intake. Latent class analysis and hierarchical linear regression models were performed to investigate the association between baseline dietary Mg, Mg trajectories, and brain volumes and WMLs. Associations between baseline Mg, and baseline blood pressure (BP) measures, and baseline Mg, Mg trajectories and BP changes (between baseline and wave 2) were also investigated to assess whether BP mediates the link between Mg intake and brain health. All analyses controlled for health and socio-demographic covariates. Possible interactions between menopausal status and Mg trajectories in predicting brain volumes and WMLs were also investigated. RESULTS: On average, higher baseline dietary Mg intake was associated with larger brain volumes (gray matter [GM]: 0.001% [SE = 0.0003]; left hippocampus [LHC]: 0.0013% [SE = 0.0006]; and right hippocampus [RHC]: 0.0023% [SE = 0.0006]) in both men and women. Latent class analysis of Mg intake revealed three classes: “high-decreasing” (men = 3.2%, women = 1.9%), “low-increasing” (men = 1.09%, women = 1.62%), and “stable normal” (men = 95.71%, women = 96.51%). In women, only the “high-decreasing” trajectory was significantly associated with larger brain volumes (GM: 1.17%, [SE = 0.58]; and RHC: 2.79% [SE = 1.11]) compared to the “normal-stable”, the “low-increasing” trajectory was associated with smaller brain volumes (GM: − 1.67%, [SE = 0.30]; white matter [WM]: − 0.85% [SE = 0.42]; LHC: − 2.43% [SE = 0.59]; and RHC: − 1.50% [SE = 0.57]) and larger WMLs (1.6% [SE = 0.53]). Associations between Mg and BP measures were mostly non-significant. Furthermore, the observed neuroprotective effect of higher dietary Mg intake in the “high-decreasing” trajectory appears to be greater in post-menopausal than pre-menopausal women. CONCLUSIONS: Higher dietary Mg intake is related to better brain health in the general population, and particularly in women. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00394-023-03123-x. Springer Berlin Heidelberg 2023-03-10 2023 /pmc/articles/PMC10349698/ /pubmed/36899275 http://dx.doi.org/10.1007/s00394-023-03123-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Contribution
Alateeq, Khawlah
Walsh, Erin I.
Cherbuin, Nicolas
Dietary magnesium intake is related to larger brain volumes and lower white matter lesions with notable sex differences
title Dietary magnesium intake is related to larger brain volumes and lower white matter lesions with notable sex differences
title_full Dietary magnesium intake is related to larger brain volumes and lower white matter lesions with notable sex differences
title_fullStr Dietary magnesium intake is related to larger brain volumes and lower white matter lesions with notable sex differences
title_full_unstemmed Dietary magnesium intake is related to larger brain volumes and lower white matter lesions with notable sex differences
title_short Dietary magnesium intake is related to larger brain volumes and lower white matter lesions with notable sex differences
title_sort dietary magnesium intake is related to larger brain volumes and lower white matter lesions with notable sex differences
topic Original Contribution
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10349698/
https://www.ncbi.nlm.nih.gov/pubmed/36899275
http://dx.doi.org/10.1007/s00394-023-03123-x
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