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Effects of ANK3 Variation on Gray and White Matter in Bipolar Disorder

The single nucleotide polymorphism rs9804190 in the Ankyrin G (ANK3) gene has been reported in genome-wide association studies to be associated with bipolar disorder (BD). However, the neural system effects of rs9804190 in BD are not known. We investigated associations between rs9804190 with gray an...

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Autores principales: Lippard, Elizabeth Thomas Cox, Jensen, Kevin Patrick, Wang, Fei, Johnston, Jennifer Ann Yadon, Spencer, Linda, Pittman, Brian, Gelernter, Joel, Blumberg, Hilary Patricia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133179/
https://www.ncbi.nlm.nih.gov/pubmed/27240527
http://dx.doi.org/10.1038/mp.2016.76
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author Lippard, Elizabeth Thomas Cox
Jensen, Kevin Patrick
Wang, Fei
Johnston, Jennifer Ann Yadon
Spencer, Linda
Pittman, Brian
Gelernter, Joel
Blumberg, Hilary Patricia
author_facet Lippard, Elizabeth Thomas Cox
Jensen, Kevin Patrick
Wang, Fei
Johnston, Jennifer Ann Yadon
Spencer, Linda
Pittman, Brian
Gelernter, Joel
Blumberg, Hilary Patricia
author_sort Lippard, Elizabeth Thomas Cox
collection PubMed
description The single nucleotide polymorphism rs9804190 in the Ankyrin G (ANK3) gene has been reported in genome-wide association studies to be associated with bipolar disorder (BD). However, the neural system effects of rs9804190 in BD are not known. We investigated associations between rs9804190 with gray and white matter structure within a frontotemporal neural system implicated in BD. A total of 187 adolescent and adult European Americans were studied: a group homozygous for the C allele [52 individuals with BD and 56 controls] and a T-carrier group, carrying the high risk T allele (38 BD and 41 controls). Subjects participated in high-resolution structural magnetic resonance imaging and diffusion tensor imaging (DTI) scanning. Frontotemporal region of interest (ROI) and whole brain exploratory analyses were conducted. DTI ROI-based analysis revealed a significant diagnosis by genotype interaction within the uncinate fasciculus (p ≥ 0.05), with BD subjects carrying the T (risk) allele showing decreased fractional anisotropy compared to other subgroups, independent of age. Genotype effects were not observed in frontotemporal gray matter volume. These findings support effects of rs9804190 on frontotemporal white matter in adolescents and adults with BD and suggest a mechanism contributing to white matter pathology in BD.
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spelling pubmed-51331792016-12-02 Effects of ANK3 Variation on Gray and White Matter in Bipolar Disorder Lippard, Elizabeth Thomas Cox Jensen, Kevin Patrick Wang, Fei Johnston, Jennifer Ann Yadon Spencer, Linda Pittman, Brian Gelernter, Joel Blumberg, Hilary Patricia Mol Psychiatry Article The single nucleotide polymorphism rs9804190 in the Ankyrin G (ANK3) gene has been reported in genome-wide association studies to be associated with bipolar disorder (BD). However, the neural system effects of rs9804190 in BD are not known. We investigated associations between rs9804190 with gray and white matter structure within a frontotemporal neural system implicated in BD. A total of 187 adolescent and adult European Americans were studied: a group homozygous for the C allele [52 individuals with BD and 56 controls] and a T-carrier group, carrying the high risk T allele (38 BD and 41 controls). Subjects participated in high-resolution structural magnetic resonance imaging and diffusion tensor imaging (DTI) scanning. Frontotemporal region of interest (ROI) and whole brain exploratory analyses were conducted. DTI ROI-based analysis revealed a significant diagnosis by genotype interaction within the uncinate fasciculus (p ≥ 0.05), with BD subjects carrying the T (risk) allele showing decreased fractional anisotropy compared to other subgroups, independent of age. Genotype effects were not observed in frontotemporal gray matter volume. These findings support effects of rs9804190 on frontotemporal white matter in adolescents and adults with BD and suggest a mechanism contributing to white matter pathology in BD. 2016-05-31 2017-09 /pmc/articles/PMC5133179/ /pubmed/27240527 http://dx.doi.org/10.1038/mp.2016.76 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Lippard, Elizabeth Thomas Cox
Jensen, Kevin Patrick
Wang, Fei
Johnston, Jennifer Ann Yadon
Spencer, Linda
Pittman, Brian
Gelernter, Joel
Blumberg, Hilary Patricia
Effects of ANK3 Variation on Gray and White Matter in Bipolar Disorder
title Effects of ANK3 Variation on Gray and White Matter in Bipolar Disorder
title_full Effects of ANK3 Variation on Gray and White Matter in Bipolar Disorder
title_fullStr Effects of ANK3 Variation on Gray and White Matter in Bipolar Disorder
title_full_unstemmed Effects of ANK3 Variation on Gray and White Matter in Bipolar Disorder
title_short Effects of ANK3 Variation on Gray and White Matter in Bipolar Disorder
title_sort effects of ank3 variation on gray and white matter in bipolar disorder
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133179/
https://www.ncbi.nlm.nih.gov/pubmed/27240527
http://dx.doi.org/10.1038/mp.2016.76
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