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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao American Journal of ...arrow_drop_down
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American Journal of Medical Genetics Part B Neuropsychiatric Genetics
Article . 2012 . Peer-reviewed
License: Wiley Online Library User Agreement
Data sources: Crossref
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Support for involvement of glutamate decarboxylase 1 and neuropeptide y in anxiety susceptibility

Authors: Jonas, Donner; Tessa, Sipilä; Samuli, Ripatti; Laura, Kananen; Xiangning, Chen; Kenneth S, Kendler; Jouko, Lönnqvist; +3 Authors

Support for involvement of glutamate decarboxylase 1 and neuropeptide y in anxiety susceptibility

Abstract

AbstractGenetic mapping efforts have identified putative susceptibility genes for human anxiety disorders. The most intensively studied genes are involved in neurotransmitter metabolism and signaling or stress response. In addition, neuropeptides and targets of anxiolytics have been examined. It has become apparent that gene × environment interactions may explain individual variation in stress resilience and predisposition to mental disorders. We aimed to replicate previous genetic findings in 16 putative anxiety susceptibility genes and further test whether they modulate the risk for developing an anxiety disorder in adulthood after childhood stress exposure. We tested 93 single‐nucleotide polymorphisms (SNPs) for genetic association to anxiety disorders in the Finnish population‐based Health 2000 sample (282 cases and 575 matched controls). In addition, we examined by logistic regression modeling whether the SNP genotypes modified the effect of the number of self‐reported childhood adversities on anxiety disorder risk. The most significant evidence for association was observed in glutamate decarboxylase 1 (GAD1) with phobias (P = 0.0005). A subsequent meta‐analysis (N = 1985) incorporating previously published findings supported involvement of a single GAD1 risk haplotype in determining susceptibility to a broad range of internalizing disorders (P = 0.0009). We additionally found that SNPs and haplotypes in neuropeptide Y (NPY) modified the effect of childhood adversities on anxiety susceptibility (P = 0.003). In conclusion, we provide further support for involvement of mainly GAD1, but also NPY in determining predisposition to anxiety disorders. © 2012 Wiley Periodicals, Inc.

Keywords

Adult, Male, Base Sequence, Genome, Human, Glutamate Decarboxylase, Molecular Sequence Data, Anxiety, Middle Aged, Linkage Disequilibrium, Phenotype, Haplotypes, Meta-Analysis as Topic, Humans, Female, Genetic Predisposition to Disease, Neuropeptide Y, Child Abuse, Child, Genetic Association Studies, Demography

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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
36
Top 10%
Top 10%
Top 10%