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Genome-wide autozygosity is associated with lower general cognitive ability.
Howrigan, D P; Simonson, M A; Davies, G; Harris, S E; Tenesa, A; Starr, J M; Liewald, D C; Deary, I J; McRae, A; Wright, M J; Montgomery, G W; Hansell, N; Martin, N G; Payton, A; Horan, M; Ollier, W E; Abdellaoui, A; Boomsma, D I; DeRosse, P; Knowles, E E M; Glahn, D C; Djurovic, S; Melle, I; Andreassen, O A; Christoforou, A; Steen, V M; Hellard, S L; Sundet, K; Reinvang, I; Espeseth, T; Lundervold, A J; Giegling, I; Konte, B; Hartmann, A M; Rujescu, D; Roussos, P; Giakoumaki, S; Burdick, K E; Bitsios, P; Donohoe, G; Corley, R P; Visscher, P M; Pendleton, N; Malhotra, A K; Neale, B M; Lencz, T; Keller, M C.
Afiliação
  • Howrigan DP; Analytic and Translational Genetics Unit, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
  • Simonson MA; Stanley Center for Psychiatric Genetics, Broad Institute of Harvard and MIT, Cambridge Center, Cambridge, MA, USA.
  • Davies G; Division of Data Sciences, Massachusetts Institute of Technology, Cambridge, MA, USA.
  • Harris SE; Department of Psychology, University of Edinburgh, Edinburgh, UK.
  • Tenesa A; Centre for Cognitive Ageing and Cognitive Epidemiology, University of Edinburgh, Edinburgh, UK.
  • Starr JM; Medical Genetics Section, University of Edinburgh Centre for Genomic and Experimental Medicine and MRC Institute of Genetics and Molecular Medicine, Western General Hospital, Edinburgh, UK.
  • Liewald DC; Institute of Genetics and Molecular Medicine, MRC Human Genetics Unit, Western General Hospital, University of Edinburgh, Edinburgh, UK.
  • Deary IJ; The Roslin Institute, Royal (Dick) School of Veterinary Studies, University of Edinburgh, Roslin, UK.
  • McRae A; Centre for Cognitive Ageing and Cognitive Epidemiology, University of Edinburgh, Edinburgh, UK.
  • Wright MJ; Alzheimer Scotland Dementia Research Centre, University of Edinburgh, Edinburgh, UK.
  • Montgomery GW; Centre for Cognitive Ageing and Cognitive Epidemiology, University of Edinburgh, Edinburgh, UK.
  • Hansell N; Department of Psychology, University of Edinburgh, Edinburgh, UK.
  • Martin NG; Centre for Cognitive Ageing and Cognitive Epidemiology, University of Edinburgh, Edinburgh, UK.
  • Payton A; Queensland Institute of Medical Research Berghofer, Brisbane, QLD, Australia.
  • Horan M; Queensland Brain Institute, The University of Queensland, Brisbane, QLD, Australia.
  • Ollier WE; Queensland Institute of Medical Research Berghofer, Brisbane, QLD, Australia.
  • Abdellaoui A; Queensland Institute of Medical Research Berghofer, Brisbane, QLD, Australia.
  • Boomsma DI; Queensland Institute of Medical Research Berghofer, Brisbane, QLD, Australia.
  • DeRosse P; Queensland Institute of Medical Research Berghofer, Brisbane, QLD, Australia.
  • Knowles EE; Centre for Integrated Genomic Medical Research, Institute of Population Health, University of Manchester, Manchester, UK.
  • Glahn DC; Centre for Clinical and Cognitive Neurosciences, Institute of Brain Behaviour and Mental Health, University of Manchester, Salford Royal NHS Foundation Trust, Salford, UK.
  • Djurovic S; Centre for Integrated Genomic Medical Research, Institute of Population Health, University of Manchester, Manchester, UK.
  • Melle I; Department of Biological Psychology, VU University Amsterdam, Amsterdam, The Netherlands.
  • Andreassen OA; Neuroscience Campus Amsterdam, Amsterdam, The Netherlands.
  • Christoforou A; Department of Biological Psychology, VU University Amsterdam, Amsterdam, The Netherlands.
  • Steen VM; Neuroscience Campus Amsterdam, Amsterdam, The Netherlands.
  • Hellard SL; EMGO+ Institute for Health and Care Research, Amsterdam, The Netherlands.
  • Sundet K; Division of Psychiatry Research, Zucker Hillside Hospital, Glen Oaks, NY, USA.
  • Reinvang I; Center for Psychiatric Neuroscience, Feinstein Institute for Medical Research, Manhasset, NY, USA.
  • Espeseth T; Hofstra North Shore - LIJ School of Medicine, Departments of Psychiatry and Molecular Medicine, Hempstead, NY, USA.
  • Lundervold AJ; Department of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.
  • Giegling I; Department of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.
  • Konte B; NORMENT, KG Jebsen Centre, Oslo, Norway.
  • Hartmann AM; Oslo University Hospital, Oslo, Norway.
  • Rujescu D; NORMENT, KG Jebsen Centre, Oslo, Norway.
  • Roussos P; Oslo University Hospital, Oslo, Norway.
  • Giakoumaki S; University of Oslo, Oslo, Norway.
  • Burdick KE; NORMENT, KG Jebsen Centre, Oslo, Norway.
  • Bitsios P; Oslo University Hospital, Oslo, Norway.
  • Donohoe G; University of Oslo, Oslo, Norway.
  • Corley RP; K.G. Jebsen Centre for Psychosis Research, Dr. Einar Martens Research Group for Biological Psychiatry, Department of Clinical Medicine, University of Bergen, Bergen, Norway.
  • Visscher PM; Center for Medical Genetics and Molecular Medicine, Haukeland University Hospital, Bergen, Norway.
  • Pendleton N; K.G. Jebsen Centre for Psychosis Research, Dr. Einar Martens Research Group for Biological Psychiatry, Department of Clinical Medicine, University of Bergen, Bergen, Norway.
  • Malhotra AK; Center for Medical Genetics and Molecular Medicine, Haukeland University Hospital, Bergen, Norway.
  • Neale BM; K.G. Jebsen Centre for Psychosis Research, Dr. Einar Martens Research Group for Biological Psychiatry, Department of Clinical Medicine, University of Bergen, Bergen, Norway.
  • Lencz T; Center for Medical Genetics and Molecular Medicine, Haukeland University Hospital, Bergen, Norway.
  • Keller MC; NORMENT, KG Jebsen Centre, Oslo, Norway.
Mol Psychiatry ; 21(6): 837-43, 2016 06.
Article em En | MEDLINE | ID: mdl-26390830
ABSTRACT
Inbreeding depression refers to lower fitness among offspring of genetic relatives. This reduced fitness is caused by the inheritance of two identical chromosomal segments (autozygosity) across the genome, which may expose the effects of (partially) recessive deleterious mutations. Even among outbred populations, autozygosity can occur to varying degrees due to cryptic relatedness between parents. Using dense genome-wide single-nucleotide polymorphism (SNP) data, we examined the degree to which autozygosity associated with measured cognitive ability in an unselected sample of 4854 participants of European ancestry. We used runs of homozygosity-multiple homozygous SNPs in a row-to estimate autozygous tracts across the genome. We found that increased levels of autozygosity predicted lower general cognitive ability, and estimate a drop of 0.6 s.d. among the offspring of first cousins (P=0.003-0.02 depending on the model). This effect came predominantly from long and rare autozygous tracts, which theory predicts as more likely to be deleterious than short and common tracts. Association mapping of autozygous tracts did not reveal any specific regions that were predictive beyond chance after correcting for multiple testing genome wide. The observed effect size is consistent with studies of cognitive decline among offspring of known consanguineous relationships. These findings suggest a role for multiple recessive or partially recessive alleles in general cognitive ability, and that alleles decreasing general cognitive ability have been selected against over evolutionary time.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cognição / Depressão por Endogamia Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male Idioma: En Revista: Mol Psychiatry Assunto da revista: BIOLOGIA MOLECULAR / PSIQUIATRIA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cognição / Depressão por Endogamia Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male Idioma: En Revista: Mol Psychiatry Assunto da revista: BIOLOGIA MOLECULAR / PSIQUIATRIA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Estados Unidos