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A Combined Pathway and Regional Heritability Analysis Indicates NETRIN1 Pathway Is Associated With Major Depressive Disorder

BACKGROUND: Genome-wide association studies (GWASs) of major depressive disorder (MDD) have identified few significant associations. Testing the aggregation of genetic variants, in particular biological pathways, may be more powerful. Regional heritability analysis can be used to detect genomic regi...

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Autores principales: Zeng, Yanni, Navarro, Pau, Fernandez-Pujals, Ana M., Hall, Lynsey S., Clarke, Toni-Kim, Thomson, Pippa A., Smith, Blair H., Hocking, Lynne J., Padmanabhan, Sandosh, Hayward, Caroline, MacIntyre, Donald J., Wray, Naomi R., Deary, Ian J., Porteous, David J., Haley, Chris S., McIntosh, Andrew M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5262437/
https://www.ncbi.nlm.nih.gov/pubmed/27422368
http://dx.doi.org/10.1016/j.biopsych.2016.04.017
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author Zeng, Yanni
Navarro, Pau
Fernandez-Pujals, Ana M.
Hall, Lynsey S.
Clarke, Toni-Kim
Thomson, Pippa A.
Smith, Blair H.
Hocking, Lynne J.
Padmanabhan, Sandosh
Hayward, Caroline
MacIntyre, Donald J.
Wray, Naomi R.
Deary, Ian J.
Porteous, David J.
Haley, Chris S.
McIntosh, Andrew M.
author_facet Zeng, Yanni
Navarro, Pau
Fernandez-Pujals, Ana M.
Hall, Lynsey S.
Clarke, Toni-Kim
Thomson, Pippa A.
Smith, Blair H.
Hocking, Lynne J.
Padmanabhan, Sandosh
Hayward, Caroline
MacIntyre, Donald J.
Wray, Naomi R.
Deary, Ian J.
Porteous, David J.
Haley, Chris S.
McIntosh, Andrew M.
author_sort Zeng, Yanni
collection PubMed
description BACKGROUND: Genome-wide association studies (GWASs) of major depressive disorder (MDD) have identified few significant associations. Testing the aggregation of genetic variants, in particular biological pathways, may be more powerful. Regional heritability analysis can be used to detect genomic regions that contribute to disease risk. METHODS: We integrated pathway analysis and multilevel regional heritability analyses in a pipeline designed to identify MDD-associated pathways. The pipeline was applied to two independent GWAS samples [Generation Scotland: The Scottish Family Health Study (GS:SFHS, N = 6455) and Psychiatric Genomics Consortium (PGC:MDD) (N = 18,759)]. A polygenic risk score (PRS) composed of single nucleotide polymorphisms from the pathway most consistently associated with MDD was created, and its accuracy to predict MDD, using area under the curve, logistic regression, and linear mixed model analyses, was tested. RESULTS: In GS:SFHS, four pathways were significantly associated with MDD, and two of these explained a significant amount of pathway-level regional heritability. In PGC:MDD, one pathway was significantly associated with MDD. Pathway-level regional heritability was significant in this pathway in one subset of PGC:MDD. For both samples the regional heritabilities were further localized to the gene and subregion levels. The NETRIN1 signaling pathway showed the most consistent association with MDD across the two samples. PRSs from this pathway showed competitive predictive accuracy compared with the whole-genome PRSs when using area under the curve statistics, logistic regression, and linear mixed model. CONCLUSIONS: These post-GWAS analyses highlight the value of combining multiple methods on multiple GWAS data for the identification of risk pathways for MDD. The NETRIN1 signaling pathway is identified as a candidate pathway for MDD and should be explored in further large population studies.
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spelling pubmed-52624372017-02-15 A Combined Pathway and Regional Heritability Analysis Indicates NETRIN1 Pathway Is Associated With Major Depressive Disorder Zeng, Yanni Navarro, Pau Fernandez-Pujals, Ana M. Hall, Lynsey S. Clarke, Toni-Kim Thomson, Pippa A. Smith, Blair H. Hocking, Lynne J. Padmanabhan, Sandosh Hayward, Caroline MacIntyre, Donald J. Wray, Naomi R. Deary, Ian J. Porteous, David J. Haley, Chris S. McIntosh, Andrew M. Biol Psychiatry Archival Report BACKGROUND: Genome-wide association studies (GWASs) of major depressive disorder (MDD) have identified few significant associations. Testing the aggregation of genetic variants, in particular biological pathways, may be more powerful. Regional heritability analysis can be used to detect genomic regions that contribute to disease risk. METHODS: We integrated pathway analysis and multilevel regional heritability analyses in a pipeline designed to identify MDD-associated pathways. The pipeline was applied to two independent GWAS samples [Generation Scotland: The Scottish Family Health Study (GS:SFHS, N = 6455) and Psychiatric Genomics Consortium (PGC:MDD) (N = 18,759)]. A polygenic risk score (PRS) composed of single nucleotide polymorphisms from the pathway most consistently associated with MDD was created, and its accuracy to predict MDD, using area under the curve, logistic regression, and linear mixed model analyses, was tested. RESULTS: In GS:SFHS, four pathways were significantly associated with MDD, and two of these explained a significant amount of pathway-level regional heritability. In PGC:MDD, one pathway was significantly associated with MDD. Pathway-level regional heritability was significant in this pathway in one subset of PGC:MDD. For both samples the regional heritabilities were further localized to the gene and subregion levels. The NETRIN1 signaling pathway showed the most consistent association with MDD across the two samples. PRSs from this pathway showed competitive predictive accuracy compared with the whole-genome PRSs when using area under the curve statistics, logistic regression, and linear mixed model. CONCLUSIONS: These post-GWAS analyses highlight the value of combining multiple methods on multiple GWAS data for the identification of risk pathways for MDD. The NETRIN1 signaling pathway is identified as a candidate pathway for MDD and should be explored in further large population studies. Elsevier 2017-02-15 /pmc/articles/PMC5262437/ /pubmed/27422368 http://dx.doi.org/10.1016/j.biopsych.2016.04.017 Text en © 2016 Society of Biological Psychiatry. All rights reserved. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Archival Report
Zeng, Yanni
Navarro, Pau
Fernandez-Pujals, Ana M.
Hall, Lynsey S.
Clarke, Toni-Kim
Thomson, Pippa A.
Smith, Blair H.
Hocking, Lynne J.
Padmanabhan, Sandosh
Hayward, Caroline
MacIntyre, Donald J.
Wray, Naomi R.
Deary, Ian J.
Porteous, David J.
Haley, Chris S.
McIntosh, Andrew M.
A Combined Pathway and Regional Heritability Analysis Indicates NETRIN1 Pathway Is Associated With Major Depressive Disorder
title A Combined Pathway and Regional Heritability Analysis Indicates NETRIN1 Pathway Is Associated With Major Depressive Disorder
title_full A Combined Pathway and Regional Heritability Analysis Indicates NETRIN1 Pathway Is Associated With Major Depressive Disorder
title_fullStr A Combined Pathway and Regional Heritability Analysis Indicates NETRIN1 Pathway Is Associated With Major Depressive Disorder
title_full_unstemmed A Combined Pathway and Regional Heritability Analysis Indicates NETRIN1 Pathway Is Associated With Major Depressive Disorder
title_short A Combined Pathway and Regional Heritability Analysis Indicates NETRIN1 Pathway Is Associated With Major Depressive Disorder
title_sort combined pathway and regional heritability analysis indicates netrin1 pathway is associated with major depressive disorder
topic Archival Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5262437/
https://www.ncbi.nlm.nih.gov/pubmed/27422368
http://dx.doi.org/10.1016/j.biopsych.2016.04.017
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