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Reciprocal causation models of cognitive vs volumetric cerebral intermediate phenotypes for schizophrenia in a pan-European twin cohort.
Toulopoulou, T; van Haren, N; Zhang, X; Sham, P C; Cherny, S S; Campbell, D D; Picchioni, M; Murray, R; Boomsma, D I; Hulshoff Pol, H E; Pol, H H; Brouwer, R; Schnack, H; Fañanás, L; Sauer, H; Nenadic, I; Weisbrod, M; Cannon, T D; Kahn, R S.
Afiliação
  • Toulopoulou T; The State Key Laboratory of Brain and Cognitive Sciences, The University of Hong Kong, Hong Kong, SAR, China.
  • van Haren N; Department of Psychology, The University of Hong Kong, Hong Kong, SAR, China.
  • Zhang X; Department of Basic and Clinical Neuroscience, The Institute of Psychiatry, Psychology and Neuroscience, King's College, London, UK.
  • Sham PC; Department of Psychiatry, Brain Centre Rudolf Magnus, University Medical Centre Utrecht, Utrecht, The Netherlands.
  • Cherny SS; Department of Psychiatry, The University of Hong Kong, Hong Kong, SAR, China.
  • Campbell DD; Centre for Genomic Sciences, The University of Hong Kong, Hong Kong, SAR, China.
  • Picchioni M; The State Key Laboratory of Brain and Cognitive Sciences, The University of Hong Kong, Hong Kong, SAR, China.
  • Murray R; Department of Psychiatry, The University of Hong Kong, Hong Kong, SAR, China.
  • Boomsma DI; Centre for Genomic Sciences, The University of Hong Kong, Hong Kong, SAR, China.
  • Hulshoff Pol HE; The State Key Laboratory of Brain and Cognitive Sciences, The University of Hong Kong, Hong Kong, SAR, China.
  • Pol HH; Department of Psychiatry, The University of Hong Kong, Hong Kong, SAR, China.
  • Brouwer R; Centre for Genomic Sciences, The University of Hong Kong, Hong Kong, SAR, China.
  • Schnack H; Department of Psychiatry, The University of Hong Kong, Hong Kong, SAR, China.
  • Fañanás L; Centre for Genomic Sciences, The University of Hong Kong, Hong Kong, SAR, China.
  • Sauer H; St Andrew's Academic Centre, Cliftonville, Northampton, UK.
  • Nenadic I; Department of Forensic and Neurodevelopmental Science, Institute of Psychiatry, London, UK.
  • Weisbrod M; Department of Psychosis, King's College London, London, UK.
  • Cannon TD; Department of Biological Psychology, VU University, Amsterdam, The Netherlands.
Mol Psychiatry ; 20(11): 1386-96, 2015 Nov.
Article em En | MEDLINE | ID: mdl-25450228
ABSTRACT
In aetiologically complex illnesses such as schizophrenia, there is no direct link between genotype and phenotype. Intermediate phenotypes could help clarify the underlying biology and assist in the hunt for genetic vulnerability variants. We have previously shown that cognition shares substantial genetic variance with schizophrenia; however, it is unknown if this reflects pleiotropic effects, direct causality or some shared third factor that links both, for example, brain volume (BV) changes. We quantified the degree of net genetic overlap and tested the direction of causation between schizophrenia liability, brain structure and cognition in a pan-European schizophrenia twin cohort consisting of 1243 members from 626 pairs. Cognitive deficits lie upstream of the liability for schizophrenia with about a quarter of the variance in liability to schizophrenia explained by variation in cognitive function. BV changes lay downstream of schizophrenia liability, with 4% of BV variation explained directly by variation in liability. However, our power to determine the nature of the relationship between BV deviation and schizophrenia liability was more limited. Thus, while there was strong evidence that cognitive impairment is causal to schizophrenia liability, we are not in a position to make a similar statement about the relationship between liability and BV. This is the first study to demonstrate that schizophrenia liability is expressed partially through cognitive deficits. One prediction of the finding that BV changes lie downstream of the disease liability is that the risk loci that influence schizophrenia liability will thereafter influence BV and to a lesser extent. By way of contrast, cognitive function lies upstream of schizophrenia, thus the relevant loci will actually have a larger effect size on cognitive function than on schizophrenia. These are testable predictions.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esquizofrenia / Encéfalo / Transtornos Cognitivos / Modelos Genéticos Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: Mol Psychiatry Assunto da revista: BIOLOGIA MOLECULAR / PSIQUIATRIA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esquizofrenia / Encéfalo / Transtornos Cognitivos / Modelos Genéticos Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: Mol Psychiatry Assunto da revista: BIOLOGIA MOLECULAR / PSIQUIATRIA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: China