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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.
Afiliación
  • Zeng Y; Division of Psychiatry, University of Edinburgh, Edinburgh, United Kingdom. Electronic address: y.zeng-6@sms.ed.ac.uk.
  • Navarro P; MRC Human Genetics Unit, University of Edinburgh, Edinburgh, United Kingdom.
  • Fernandez-Pujals AM; Division of Psychiatry, University of Edinburgh, Edinburgh, United Kingdom.
  • Hall LS; Division of Psychiatry, University of Edinburgh, Edinburgh, United Kingdom.
  • Clarke TK; Division of Psychiatry, University of Edinburgh, Edinburgh, United Kingdom.
  • Thomson PA; Centre for Cognitive Ageing and Cognitive Epidemiology, University of Edinburgh, Edinburgh, United Kingdom; Medical Genetics Section, University of Edinburgh, Edinburgh, United Kingdom.
  • Smith BH; Centre for Genomic and Experimental Medicine, University of Edinburgh, Edinburgh, United Kingdom; Division of Population Health Sciences, University of Dundee, Dundee, United Kingdom.
  • Hocking LJ; Centre for Genomic and Experimental Medicine, University of Edinburgh, Edinburgh, United Kingdom; Division of Applied Health Sciences, University of Aberdeen, Aberdeen, United Kingdom.
  • Padmanabhan S; Centre for Genomic and Experimental Medicine, University of Edinburgh, Edinburgh, United Kingdom; Institute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, United Kingdom.
  • Hayward C; MRC Human Genetics Unit, University of Edinburgh, Edinburgh, United Kingdom; Centre for Genomic and Experimental Medicine, University of Edinburgh, Edinburgh, United Kingdom.
  • MacIntyre DJ; Division of Psychiatry, University of Edinburgh, Edinburgh, United Kingdom.
  • Wray NR; Queensland Brain Institute, University of Queensland, St Lucia, Queensland, Australia.
  • Deary IJ; Centre for Cognitive Ageing and Cognitive Epidemiology, University of Edinburgh, Edinburgh, United Kingdom; Generation Scotland, University of Edinburgh, Edinburgh, United Kingdom; Institute of Genetics and Molecular Medicine, Department of Psychology, University of Edinburgh, Edinburgh, United King
  • Porteous DJ; Centre for Cognitive Ageing and Cognitive Epidemiology, University of Edinburgh, Edinburgh, United Kingdom; Medical Genetics Section, University of Edinburgh, Edinburgh, United Kingdom; Generation Scotland, University of Edinburgh, Edinburgh, United Kingdom.
  • Haley CS; MRC Human Genetics Unit, University of Edinburgh, Edinburgh, United Kingdom; The Roslin Institute and Royal (Dick) School of Veterinary Sciences, University of Edinburgh, Edinburgh, United Kingdom.
  • McIntosh AM; Division of Psychiatry, University of Edinburgh, Edinburgh, United Kingdom; Centre for Cognitive Ageing and Cognitive Epidemiology, University of Edinburgh, Edinburgh, United Kingdom; Generation Scotland, University of Edinburgh, Edinburgh, United Kingdom.
Biol Psychiatry ; 81(4): 336-346, 2017 02 15.
Article en En | MEDLINE | ID: mdl-27422368
ABSTRACT

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 (GSSFHS, N = 6455) and Psychiatric Genomics Consortium (PGCMDD) (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 GSSFHS, four pathways were significantly associated with MDD, and two of these explained a significant amount of pathway-level regional heritability. In PGCMDD, one pathway was significantly associated with MDD. Pathway-level regional heritability was significant in this pathway in one subset of PGCMDD. 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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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Transducción de Señal / Predisposición Genética a la Enfermedad / Proteínas Supresoras de Tumor / Trastorno Depresivo Mayor / Factores de Crecimiento Nervioso Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Biol Psychiatry Año: 2017 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Transducción de Señal / Predisposición Genética a la Enfermedad / Proteínas Supresoras de Tumor / Trastorno Depresivo Mayor / Factores de Crecimiento Nervioso Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Biol Psychiatry Año: 2017 Tipo del documento: Article
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