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Cognitive markers of preclinical and prodromal Alzheimer's disease in Down syndrome.
Startin, Carla M; Hamburg, Sarah; Hithersay, Rosalyn; Al-Janabi, Tamara; Mok, Kin Y; Hardy, John; Strydom, Andre.
Afiliação
  • Startin CM; Department of Forensic and Neurodevelopmental Sciences, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK; Division of Psychiatry, University College London, London, UK; The LonDownS Consortium, London, UK. Electronic address: carla.startin.09@ucl.ac.uk.
  • Hamburg S; Department of Forensic and Neurodevelopmental Sciences, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK; Division of Psychiatry, University College London, London, UK; The LonDownS Consortium, London, UK.
  • Hithersay R; Department of Forensic and Neurodevelopmental Sciences, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK; Division of Psychiatry, University College London, London, UK; The LonDownS Consortium, London, UK.
  • Al-Janabi T; Division of Psychiatry, University College London, London, UK; The LonDownS Consortium, London, UK.
  • Mok KY; The LonDownS Consortium, London, UK; Department of Molecular Neuroscience, Institute of Neurology, University College London, London, UK; Division of Life Science, Hong Kong University of Science and Technology, Hong Kong SAR, People's Republic of China.
  • Hardy J; The LonDownS Consortium, London, UK; Department of Molecular Neuroscience, Institute of Neurology, University College London, London, UK; Reta Lila Weston Institute, Institute of Neurology, University College London, London, UK.
  • Strydom A; Department of Forensic and Neurodevelopmental Sciences, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK; Division of Psychiatry, University College London, London, UK; The LonDownS Consortium, London, UK.
Alzheimers Dement ; 15(2): 245-257, 2019 02.
Article em En | MEDLINE | ID: mdl-30503169
ABSTRACT

INTRODUCTION:

Down syndrome (DS) is associated with an almost universal development of Alzheimer's disease. Individuals with DS are therefore an important population for randomized controlled trials to prevent or delay cognitive decline, though it is essential to understand the time course of early cognitive changes.

METHODS:

We conducted the largest cognitive study to date with 312 adults with DS to assess age-related and Alzheimer's disease-related cognitive changes during progression from preclinical to prodromal dementia, and prodromal to clinical dementia.

RESULTS:

Changes in memory and attention measures were most sensitive to early decline. Resulting sample size calculations for randomized controlled trials to detect significant treatment effects to delay decline were modest.

DISCUSSION:

Our findings address uncertainties around the development of randomized controlled trials to delay cognitive decline in DS. Such trials are essential to reduce the high burden of dementia in people with DS and could serve as proof-of-principle trials for some drug targets.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Biomarcadores / Síndrome de Down / Doença de Alzheimer / Disfunção Cognitiva / Sintomas Prodrômicos Tipo de estudo: Clinical_trials Limite: Adolescent / Adult / Female / Humans / Middle aged Idioma: En Revista: Alzheimers Dement Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Biomarcadores / Síndrome de Down / Doença de Alzheimer / Disfunção Cognitiva / Sintomas Prodrômicos Tipo de estudo: Clinical_trials Limite: Adolescent / Adult / Female / Humans / Middle aged Idioma: En Revista: Alzheimers Dement Ano de publicação: 2019 Tipo de documento: Article