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Accelerated aging in the brain, epigenetic aging in blood, and polygenic risk for schizophrenia.
Teeuw, Jalmar; Ori, Anil P S; Brouwer, Rachel M; de Zwarte, Sonja M C; Schnack, Hugo G; Hulshoff Pol, Hilleke E; Ophoff, Roel A.
Afiliação
  • Teeuw J; Department of Psychiatry, UMC Brain Center, University Medical Center Utrecht, Utrecht, the Netherlands. Electronic address: j.teeuw@umcutrecht.nl.
  • Ori APS; Center for Neurobehavioral Genetics, University of California, Los Angeles, United States.
  • Brouwer RM; Department of Psychiatry, UMC Brain Center, University Medical Center Utrecht, Utrecht, the Netherlands.
  • de Zwarte SMC; Department of Psychiatry, UMC Brain Center, University Medical Center Utrecht, Utrecht, the Netherlands.
  • Schnack HG; Department of Psychiatry, UMC Brain Center, University Medical Center Utrecht, Utrecht, the Netherlands.
  • Hulshoff Pol HE; Department of Psychiatry, UMC Brain Center, University Medical Center Utrecht, Utrecht, the Netherlands.
  • Ophoff RA; Center for Neurobehavioral Genetics, University of California, Los Angeles, United States; Department of Psychiatry, Erasmus University Medical Center, Rotterdam, the Netherlands.
Schizophr Res ; 231: 189-197, 2021 05.
Article em En | MEDLINE | ID: mdl-33882370
ABSTRACT
Schizophrenia patients show signs of accelerated aging in cognitive and physiological domains. Both schizophrenia and accelerated aging, as measured by MRI brain images and epigenetic clocks, are correlated with increased mortality. However, the association between these aging measures have not yet been studied in schizophrenia patients. In schizophrenia patients and healthy subjects, accelerated aging was assessed in brain tissue using a longitudinal MRI (N = 715 scans; mean scan interval 3.4 year) and in blood using two epigenetic age clocks (N = 172). Differences ('gaps') between estimated ages and chronological ages were calculated, as well as the acceleration rate of brain aging. The correlations between these aging measures as well as with polygenic risk scores for schizophrenia (PRS; N = 394) were investigated. Brain aging and epigenetic aging were not significantly correlated. Polygenic risk for schizophrenia was significantly correlated with brain age gap, brain age acceleration rate, and negatively correlated with DNAmAge gap, but not with PhenoAge gap. However, after controlling for disease status and multiple comparisons correction, these effects were no longer significant. Our results imply that the (accelerated) aging observed in the brain and blood reflect distinct biological processes. Our findings will require replication in a larger cohort.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esquizofrenia Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esquizofrenia Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article