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Functional neuroimaging effects of recently discovered genetic risk loci for schizophrenia and polygenic risk profile in five RDoC subdomains

Recently, 125 loci with genome-wide support for association with schizophrenia were identified. We investigated the impact of these variants and their accumulated genetic risk on brain activation in five neurocognitive domains of the Research Domain Criteria (working memory, reward processing, episo...

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Autores principales: Erk, S, Mohnke, S, Ripke, S, Lett, T A, Veer, I M, Wackerhagen, C, Grimm, O, Romanczuk-Seiferth, N, Degenhardt, F, Tost, H, Mattheisen, M, Mühleisen, T W, Charlet, K, Skarabis, N, Kiefer, F, Cichon, S, Witt, S H, Nöthen, M M, Rietschel, M, Heinz, A, Meyer-Lindenberg, A, Walter, H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5545733/
https://www.ncbi.nlm.nih.gov/pubmed/28072415
http://dx.doi.org/10.1038/tp.2016.272
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author Erk, S
Mohnke, S
Ripke, S
Lett, T A
Veer, I M
Wackerhagen, C
Grimm, O
Romanczuk-Seiferth, N
Degenhardt, F
Tost, H
Mattheisen, M
Mühleisen, T W
Charlet, K
Skarabis, N
Kiefer, F
Cichon, S
Witt, S H
Nöthen, M M
Rietschel, M
Heinz, A
Meyer-Lindenberg, A
Walter, H
author_facet Erk, S
Mohnke, S
Ripke, S
Lett, T A
Veer, I M
Wackerhagen, C
Grimm, O
Romanczuk-Seiferth, N
Degenhardt, F
Tost, H
Mattheisen, M
Mühleisen, T W
Charlet, K
Skarabis, N
Kiefer, F
Cichon, S
Witt, S H
Nöthen, M M
Rietschel, M
Heinz, A
Meyer-Lindenberg, A
Walter, H
author_sort Erk, S
collection PubMed
description Recently, 125 loci with genome-wide support for association with schizophrenia were identified. We investigated the impact of these variants and their accumulated genetic risk on brain activation in five neurocognitive domains of the Research Domain Criteria (working memory, reward processing, episodic memory, social cognition and emotion processing). In 578 healthy subjects we tested for association (i) of a polygenic risk profile score (RPS) including all single-nucleotide polymorphisms (SNPs) reaching genome-wide significance in the recent genome-wide association studies (GWAS) meta-analysis and (ii) of all independent genome-wide significant loci separately that showed sufficient distribution of all allelic groups in our sample (105 SNPs). The RPS was nominally associated with perigenual anterior cingulate and posterior cingulate/precuneus activation during episodic memory (P(FWE(ROI))=0.047) and social cognition (P(FWE(ROI))=0.025), respectively. Single SNP analyses revealed that rs9607782, located near EP300, was significantly associated with amygdala recruitment during emotion processing (P(FWE)((ROI))=1.63 × 10(−4), surpassing Bonferroni correction for the number of SNPs). Importantly, this association was replicable in an independent sample (N=150; P(FWE)((ROI))<0.025). Other SNP effects previously associated with imaging phenotypes were nominally significant, but did not withstand correction for the number of SNPs tested. To assess whether there was true signal within our data, we repeated single SNP analyses with 105 randomly chosen non-schizophrenia-associated variants, observing fewer significant results and lower association probabilities. Applying stringent methodological procedures, we found preliminary evidence for the notion that genetic risk for schizophrenia conferred by rs9607782 may be mediated by amygdala function. We critically evaluate the potential caveats of the methodological approaches employed and offer suggestions for future studies.
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spelling pubmed-55457332017-08-07 Functional neuroimaging effects of recently discovered genetic risk loci for schizophrenia and polygenic risk profile in five RDoC subdomains Erk, S Mohnke, S Ripke, S Lett, T A Veer, I M Wackerhagen, C Grimm, O Romanczuk-Seiferth, N Degenhardt, F Tost, H Mattheisen, M Mühleisen, T W Charlet, K Skarabis, N Kiefer, F Cichon, S Witt, S H Nöthen, M M Rietschel, M Heinz, A Meyer-Lindenberg, A Walter, H Transl Psychiatry Original Article Recently, 125 loci with genome-wide support for association with schizophrenia were identified. We investigated the impact of these variants and their accumulated genetic risk on brain activation in five neurocognitive domains of the Research Domain Criteria (working memory, reward processing, episodic memory, social cognition and emotion processing). In 578 healthy subjects we tested for association (i) of a polygenic risk profile score (RPS) including all single-nucleotide polymorphisms (SNPs) reaching genome-wide significance in the recent genome-wide association studies (GWAS) meta-analysis and (ii) of all independent genome-wide significant loci separately that showed sufficient distribution of all allelic groups in our sample (105 SNPs). The RPS was nominally associated with perigenual anterior cingulate and posterior cingulate/precuneus activation during episodic memory (P(FWE(ROI))=0.047) and social cognition (P(FWE(ROI))=0.025), respectively. Single SNP analyses revealed that rs9607782, located near EP300, was significantly associated with amygdala recruitment during emotion processing (P(FWE)((ROI))=1.63 × 10(−4), surpassing Bonferroni correction for the number of SNPs). Importantly, this association was replicable in an independent sample (N=150; P(FWE)((ROI))<0.025). Other SNP effects previously associated with imaging phenotypes were nominally significant, but did not withstand correction for the number of SNPs tested. To assess whether there was true signal within our data, we repeated single SNP analyses with 105 randomly chosen non-schizophrenia-associated variants, observing fewer significant results and lower association probabilities. Applying stringent methodological procedures, we found preliminary evidence for the notion that genetic risk for schizophrenia conferred by rs9607782 may be mediated by amygdala function. We critically evaluate the potential caveats of the methodological approaches employed and offer suggestions for future studies. Nature Publishing Group 2017-01 2017-01-10 /pmc/articles/PMC5545733/ /pubmed/28072415 http://dx.doi.org/10.1038/tp.2016.272 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Original Article
Erk, S
Mohnke, S
Ripke, S
Lett, T A
Veer, I M
Wackerhagen, C
Grimm, O
Romanczuk-Seiferth, N
Degenhardt, F
Tost, H
Mattheisen, M
Mühleisen, T W
Charlet, K
Skarabis, N
Kiefer, F
Cichon, S
Witt, S H
Nöthen, M M
Rietschel, M
Heinz, A
Meyer-Lindenberg, A
Walter, H
Functional neuroimaging effects of recently discovered genetic risk loci for schizophrenia and polygenic risk profile in five RDoC subdomains
title Functional neuroimaging effects of recently discovered genetic risk loci for schizophrenia and polygenic risk profile in five RDoC subdomains
title_full Functional neuroimaging effects of recently discovered genetic risk loci for schizophrenia and polygenic risk profile in five RDoC subdomains
title_fullStr Functional neuroimaging effects of recently discovered genetic risk loci for schizophrenia and polygenic risk profile in five RDoC subdomains
title_full_unstemmed Functional neuroimaging effects of recently discovered genetic risk loci for schizophrenia and polygenic risk profile in five RDoC subdomains
title_short Functional neuroimaging effects of recently discovered genetic risk loci for schizophrenia and polygenic risk profile in five RDoC subdomains
title_sort functional neuroimaging effects of recently discovered genetic risk loci for schizophrenia and polygenic risk profile in five rdoc subdomains
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5545733/
https://www.ncbi.nlm.nih.gov/pubmed/28072415
http://dx.doi.org/10.1038/tp.2016.272
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