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Identifying individuals with high risk of Alzheimer's disease using polygenic risk scores.
Leonenko, Ganna; Baker, Emily; Stevenson-Hoare, Joshua; Sierksma, Annerieke; Fiers, Mark; Williams, Julie; de Strooper, Bart; Escott-Price, Valentina.
Afiliação
  • Leonenko G; UK Dementia Research Institute, Cardiff University, Cardiff, UK.
  • Baker E; UK Dementia Research Institute, Cardiff University, Cardiff, UK.
  • Stevenson-Hoare J; UK Dementia Research Institute, Cardiff University, Cardiff, UK.
  • Sierksma A; VIB Center for Brain & Disease Research, Leuven, Belgium.
  • Fiers M; Laboratory for the Research of Neurodegenerative Diseases, Department of Neurosciences, Leuven Brain Institute (LBI), KU Leuven (University of Leuven), Leuven, Belgium.
  • Williams J; VIB Center for Brain & Disease Research, Leuven, Belgium.
  • de Strooper B; Laboratory for the Research of Neurodegenerative Diseases, Department of Neurosciences, Leuven Brain Institute (LBI), KU Leuven (University of Leuven), Leuven, Belgium.
  • Escott-Price V; UK Dementia Research Institute, University College London, London, UK.
Nat Commun ; 12(1): 4506, 2021 07 23.
Article em En | MEDLINE | ID: mdl-34301930
ABSTRACT
Polygenic Risk Scores (PRS) for AD offer unique possibilities for reliable identification of individuals at high and low risk of AD. However, there is little agreement in the field as to what approach should be used for genetic risk score calculations, how to model the effect of APOE, what the optimal p-value threshold (pT) for SNP selection is and how to compare scores between studies and methods. We show that the best prediction accuracy is achieved with a model with two predictors (APOE and PRS excluding APOE region) with pT<0.1 for SNP selection. Prediction accuracy in a sample across different PRS approaches is similar, but individuals' scores and their associated ranking differ. We show that standardising PRS against the population mean, as opposed to the sample mean, makes the individuals' scores comparable between studies. Our work highlights the best strategies for polygenic profiling when assessing individuals for AD risk.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Apolipoproteínas E / Herança Multifatorial / Polimorfismo de Nucleotídeo Único / Estudo de Associação Genômica Ampla / Doença de Alzheimer Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Aspecto: Patient_preference Limite: Humans Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Apolipoproteínas E / Herança Multifatorial / Polimorfismo de Nucleotídeo Único / Estudo de Associação Genômica Ampla / Doença de Alzheimer Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Aspecto: Patient_preference Limite: Humans Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Reino Unido