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The α-endomannosidase gene (MANEA) is associated with panic disorder and social anxiety disorder
Unbiased genome-wide approaches can provide novel insights into the biological pathways that are important for human behavior and psychiatric disorder risk. The association of α-endomannosidase gene (MANEA) variants and cocaine-induced paranoia (CIP) was initially described in a study that used a wh...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3905232/ https://www.ncbi.nlm.nih.gov/pubmed/24473444 http://dx.doi.org/10.1038/tp.2013.122 |
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author | Jensen, K P Stein, M B Kranzler, H R Yang, B Z Farrer, L A Gelernter, J |
author_facet | Jensen, K P Stein, M B Kranzler, H R Yang, B Z Farrer, L A Gelernter, J |
author_sort | Jensen, K P |
collection | PubMed |
description | Unbiased genome-wide approaches can provide novel insights into the biological pathways that are important for human behavior and psychiatric disorder risk. The association of α-endomannosidase gene (MANEA) variants and cocaine-induced paranoia (CIP) was initially described in a study that used a whole-genome approach. Behavioral effects have been reported for other mannosidase genes, but MANEA function in humans and the clinical potential of the previous findings remain unclear. We hypothesized that MANEA would be associated with psychiatric phenotypes unrelated to cocaine use. We used a multi-stage association study approach starting with four psychiatric disorders to show an association between a MANEA single-nucleotide polymorphism (SNP; rs1133503) and anxiety disorders. In the first study of 2073 European American (EA) and 2459 African American subjects mostly with comorbid drug or alcohol dependence, we observed an association in EAs of rs1133503 with panic disorder (PD) (191 PD cases, odds ratio (OR)=1.7 (95% confidence interval (CI): 1.22–2.41), P=0.002). We replicated this finding in an independent sample of 142 PD cases (OR =1.53 (95% CI: 1.00–2.31), P=0.043) and extended it in an independent sample of 131 generalized social anxiety disorder cases (OR=2.15 (95% CI: 1.27–3.64), P=0.004). MANEA alleles and genotypes were also associated with gene expression differences in whole blood cells. Using publically available data, we observed a consistent effect on expression in brain tissue. We conclude that pathways involving α-endomannosidase warrant further investigation in relation to anxiety disorders. |
format | Online Article Text |
id | pubmed-3905232 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-39052322014-01-29 The α-endomannosidase gene (MANEA) is associated with panic disorder and social anxiety disorder Jensen, K P Stein, M B Kranzler, H R Yang, B Z Farrer, L A Gelernter, J Transl Psychiatry Original Article Unbiased genome-wide approaches can provide novel insights into the biological pathways that are important for human behavior and psychiatric disorder risk. The association of α-endomannosidase gene (MANEA) variants and cocaine-induced paranoia (CIP) was initially described in a study that used a whole-genome approach. Behavioral effects have been reported for other mannosidase genes, but MANEA function in humans and the clinical potential of the previous findings remain unclear. We hypothesized that MANEA would be associated with psychiatric phenotypes unrelated to cocaine use. We used a multi-stage association study approach starting with four psychiatric disorders to show an association between a MANEA single-nucleotide polymorphism (SNP; rs1133503) and anxiety disorders. In the first study of 2073 European American (EA) and 2459 African American subjects mostly with comorbid drug or alcohol dependence, we observed an association in EAs of rs1133503 with panic disorder (PD) (191 PD cases, odds ratio (OR)=1.7 (95% confidence interval (CI): 1.22–2.41), P=0.002). We replicated this finding in an independent sample of 142 PD cases (OR =1.53 (95% CI: 1.00–2.31), P=0.043) and extended it in an independent sample of 131 generalized social anxiety disorder cases (OR=2.15 (95% CI: 1.27–3.64), P=0.004). MANEA alleles and genotypes were also associated with gene expression differences in whole blood cells. Using publically available data, we observed a consistent effect on expression in brain tissue. We conclude that pathways involving α-endomannosidase warrant further investigation in relation to anxiety disorders. Nature Publishing Group 2014-01 2014-01-28 /pmc/articles/PMC3905232/ /pubmed/24473444 http://dx.doi.org/10.1038/tp.2013.122 Text en Copyright © 2014 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Original Article Jensen, K P Stein, M B Kranzler, H R Yang, B Z Farrer, L A Gelernter, J The α-endomannosidase gene (MANEA) is associated with panic disorder and social anxiety disorder |
title | The α-endomannosidase gene (MANEA) is associated with panic disorder and social anxiety disorder |
title_full | The α-endomannosidase gene (MANEA) is associated with panic disorder and social anxiety disorder |
title_fullStr | The α-endomannosidase gene (MANEA) is associated with panic disorder and social anxiety disorder |
title_full_unstemmed | The α-endomannosidase gene (MANEA) is associated with panic disorder and social anxiety disorder |
title_short | The α-endomannosidase gene (MANEA) is associated with panic disorder and social anxiety disorder |
title_sort | α-endomannosidase gene (manea) is associated with panic disorder and social anxiety disorder |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3905232/ https://www.ncbi.nlm.nih.gov/pubmed/24473444 http://dx.doi.org/10.1038/tp.2013.122 |
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