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Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank
Here, we investigated the genetics of weighted functional brain network graph theory measures from 18,445 participants of the UK Biobank (44–80 years). The eighteen measures studied showed low heritability (mean h(2)(SNP) = 0.12) and were highly genetically correlated. One genome-wide significant lo...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8285376/ https://www.ncbi.nlm.nih.gov/pubmed/34272439 http://dx.doi.org/10.1038/s41598-021-94182-9 |
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author | Foo, Heidi Thalamuthu, Anbupalam Jiang, Jiyang Koch, Forrest C. Mather, Karen A. Wen, Wei Sachdev, Perminder S. |
author_facet | Foo, Heidi Thalamuthu, Anbupalam Jiang, Jiyang Koch, Forrest C. Mather, Karen A. Wen, Wei Sachdev, Perminder S. |
author_sort | Foo, Heidi |
collection | PubMed |
description | Here, we investigated the genetics of weighted functional brain network graph theory measures from 18,445 participants of the UK Biobank (44–80 years). The eighteen measures studied showed low heritability (mean h(2)(SNP) = 0.12) and were highly genetically correlated. One genome-wide significant locus was associated with strength of somatomotor and limbic networks. These intergenic variants were located near the PAX8 gene on chromosome 2. Gene-based analyses identified five significantly associated genes for five of the network measures, which have been implicated in sleep duration, neuronal differentiation/development, cancer, and susceptibility to neurodegenerative diseases. Further analysis found that somatomotor network strength was phenotypically associated with sleep duration and insomnia. Single nucleotide polymorphism (SNP) and gene level associations with functional network measures were identified, which may help uncover novel biological pathways relevant to human brain functional network integrity and related disorders that affect it. |
format | Online Article Text |
id | pubmed-8285376 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82853762021-07-19 Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank Foo, Heidi Thalamuthu, Anbupalam Jiang, Jiyang Koch, Forrest C. Mather, Karen A. Wen, Wei Sachdev, Perminder S. Sci Rep Article Here, we investigated the genetics of weighted functional brain network graph theory measures from 18,445 participants of the UK Biobank (44–80 years). The eighteen measures studied showed low heritability (mean h(2)(SNP) = 0.12) and were highly genetically correlated. One genome-wide significant locus was associated with strength of somatomotor and limbic networks. These intergenic variants were located near the PAX8 gene on chromosome 2. Gene-based analyses identified five significantly associated genes for five of the network measures, which have been implicated in sleep duration, neuronal differentiation/development, cancer, and susceptibility to neurodegenerative diseases. Further analysis found that somatomotor network strength was phenotypically associated with sleep duration and insomnia. Single nucleotide polymorphism (SNP) and gene level associations with functional network measures were identified, which may help uncover novel biological pathways relevant to human brain functional network integrity and related disorders that affect it. Nature Publishing Group UK 2021-07-16 /pmc/articles/PMC8285376/ /pubmed/34272439 http://dx.doi.org/10.1038/s41598-021-94182-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This 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 | Article Foo, Heidi Thalamuthu, Anbupalam Jiang, Jiyang Koch, Forrest C. Mather, Karen A. Wen, Wei Sachdev, Perminder S. Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank |
title | Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank |
title_full | Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank |
title_fullStr | Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank |
title_full_unstemmed | Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank |
title_short | Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank |
title_sort | novel genetic variants associated with brain functional networks in 18,445 adults from the uk biobank |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8285376/ https://www.ncbi.nlm.nih.gov/pubmed/34272439 http://dx.doi.org/10.1038/s41598-021-94182-9 |
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