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Increased brain volume from higher cereal and lower coffee intake: shared genetic determinants and impacts on cognition and metabolism

It is unclear how different diets may affect human brain development and if genetic and environmental factors play a part. We investigated diet effects in the UK Biobank data from 18,879 healthy adults and discovered anticorrelated brain-wide gray matter volume (GMV)-association patterns between cof...

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Autores principales: Kang, Jujiao, Jia, Tianye, Jiao, Zeyu, Shen, Chun, Xie, Chao, Cheng, Wei, Sahakian, Barbara J, Waxman, David, Feng, Jianfeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9383440/
https://www.ncbi.nlm.nih.gov/pubmed/35136970
http://dx.doi.org/10.1093/cercor/bhac005
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author Kang, Jujiao
Jia, Tianye
Jiao, Zeyu
Shen, Chun
Xie, Chao
Cheng, Wei
Sahakian, Barbara J
Waxman, David
Feng, Jianfeng
author_facet Kang, Jujiao
Jia, Tianye
Jiao, Zeyu
Shen, Chun
Xie, Chao
Cheng, Wei
Sahakian, Barbara J
Waxman, David
Feng, Jianfeng
author_sort Kang, Jujiao
collection PubMed
description It is unclear how different diets may affect human brain development and if genetic and environmental factors play a part. We investigated diet effects in the UK Biobank data from 18,879 healthy adults and discovered anticorrelated brain-wide gray matter volume (GMV)-association patterns between coffee and cereal intake, coincidence with their anticorrelated genetic constructs. The Mendelian randomization approach further indicated a causal effect of higher coffee intake on reduced total GMV, which is likely through regulating the expression of genes responsible for synaptic development in the brain. The identified genetic factors may further affect people’s lifestyle habits and body/blood fat levels through the mediation of cereal/coffee intake, and the brain-wide expression pattern of gene CPLX3, a dedicated marker of subplate neurons that regulate cortical development and plasticity, may underlie the shared GMV-association patterns among the coffee/cereal intake and cognitive functions. All the main findings were successfully replicated. Our findings thus revealed that high-cereal and low-coffee diets shared similar brain and genetic constructs, leading to long-term beneficial associations regarding cognitive, body mass index (BMI), and other metabolic measures. This study has important implications for public health, especially during the pandemic, given the poorer outcomes of COVID-19 patients with greater BMIs.
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spelling pubmed-93834402022-08-17 Increased brain volume from higher cereal and lower coffee intake: shared genetic determinants and impacts on cognition and metabolism Kang, Jujiao Jia, Tianye Jiao, Zeyu Shen, Chun Xie, Chao Cheng, Wei Sahakian, Barbara J Waxman, David Feng, Jianfeng Cereb Cortex Original Article It is unclear how different diets may affect human brain development and if genetic and environmental factors play a part. We investigated diet effects in the UK Biobank data from 18,879 healthy adults and discovered anticorrelated brain-wide gray matter volume (GMV)-association patterns between coffee and cereal intake, coincidence with their anticorrelated genetic constructs. The Mendelian randomization approach further indicated a causal effect of higher coffee intake on reduced total GMV, which is likely through regulating the expression of genes responsible for synaptic development in the brain. The identified genetic factors may further affect people’s lifestyle habits and body/blood fat levels through the mediation of cereal/coffee intake, and the brain-wide expression pattern of gene CPLX3, a dedicated marker of subplate neurons that regulate cortical development and plasticity, may underlie the shared GMV-association patterns among the coffee/cereal intake and cognitive functions. All the main findings were successfully replicated. Our findings thus revealed that high-cereal and low-coffee diets shared similar brain and genetic constructs, leading to long-term beneficial associations regarding cognitive, body mass index (BMI), and other metabolic measures. This study has important implications for public health, especially during the pandemic, given the poorer outcomes of COVID-19 patients with greater BMIs. Oxford University Press 2022-02-07 /pmc/articles/PMC9383440/ /pubmed/35136970 http://dx.doi.org/10.1093/cercor/bhac005 Text en © The Author(s) 2022. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kang, Jujiao
Jia, Tianye
Jiao, Zeyu
Shen, Chun
Xie, Chao
Cheng, Wei
Sahakian, Barbara J
Waxman, David
Feng, Jianfeng
Increased brain volume from higher cereal and lower coffee intake: shared genetic determinants and impacts on cognition and metabolism
title Increased brain volume from higher cereal and lower coffee intake: shared genetic determinants and impacts on cognition and metabolism
title_full Increased brain volume from higher cereal and lower coffee intake: shared genetic determinants and impacts on cognition and metabolism
title_fullStr Increased brain volume from higher cereal and lower coffee intake: shared genetic determinants and impacts on cognition and metabolism
title_full_unstemmed Increased brain volume from higher cereal and lower coffee intake: shared genetic determinants and impacts on cognition and metabolism
title_short Increased brain volume from higher cereal and lower coffee intake: shared genetic determinants and impacts on cognition and metabolism
title_sort increased brain volume from higher cereal and lower coffee intake: shared genetic determinants and impacts on cognition and metabolism
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9383440/
https://www.ncbi.nlm.nih.gov/pubmed/35136970
http://dx.doi.org/10.1093/cercor/bhac005
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