The AT(N) framework for Alzheimer's disease in adults with Down syndrome.

Alzheimer's disease Down syndrome biomarkers

Journal

Alzheimer's & dementia (Amsterdam, Netherlands)
ISSN: 2352-8729
Titre abrégé: Alzheimers Dement (Amst)
Pays: United States
ID NLM: 101654604

Informations de publication

Date de publication:
2020
Historique:
received: 17 04 2020
accepted: 04 06 2020
entrez: 2 11 2020
pubmed: 3 11 2020
medline: 3 11 2020
Statut: epublish

Résumé

The National Institute on Aging in conjunction with the Alzheimer's Association (NIA-AA) recently proposed a biological framework for defining the Alzheimer's disease (AD) continuum. This new framework is based upon the key AD biomarkers (amyloid, tau, neurodegeneration, AT[N]) instead of clinical symptoms and represents the latest understanding that the pathological processes underlying AD begin decades before the manifestation of symptoms. By using these same biomarkers, individuals with Down syndrome (DS), who are genetically predisposed to developing AD, can also be placed more precisely along the AD continuum. The A/T(N) framework is therefore thought to provide an objective manner by which to select and enrich samples for clinical trials. This new framework is highly flexible and allows the addition of newly confirmed AD biomarkers into the existing AT(N) groups. As biomarkers for other pathological processes are validated, they can also be added to the AT(N) classification scheme, which will allow for better characterization and staging of AD in DS. These biological classifications can then be merged with clinical staging for an examination of factors that impact the biological and clinical progression of the disease. Here, we leverage previously published guidelines for the AT(N) framework to generate such a plan for AD among adults with DS.

Identifiants

pubmed: 33134477
doi: 10.1002/dad2.12062
pii: DAD212062
pmc: PMC7588820
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e12062

Subventions

Organisme : Medical Research Council
ID : MR/R024901/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/S011277/1
Pays : United Kingdom
Organisme : NICHD NIH HHS
ID : R01 HD064993
Pays : United States
Organisme : NIA NIH HHS
ID : U19 AG068054
Pays : United States
Organisme : NIA NIH HHS
ID : P30 AG066462
Pays : United States

Informations de copyright

© 2020 the Alzheimer's Association.

Déclaration de conflit d'intérêts

The authors report no conflicts of interest that are relevant for this manuscript.

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Auteurs

Michael S Rafii (MS)

Alzheimer's Therapeutic Research Institute (ATRI) Keck School of Medicine University of Southern California San Diego California USA.

Beau M Ances (BM)

Center for Advanced Medicine Neuroscience Washington University School of Medicine in St. Louis St. Louis Missouri USA.

Nicole Schupf (N)

Taub Institute for Research on Alzheimer's Disease and the Aging Brain/G.H. Sergievsky Center Columbia University Irving Medical Center New York New York USA.
Department of Epidemiology Mailman School of Public Health Columbia University New York New York USA.
Department of Neurology Neurological Institute of New York, Columbia University Irving Medical Center New York New York USA.
Department of Psychiatry Columbia University Medical Center New York New York USA.

Sharon J Krinsky-McHale (SJ)

Department of Psychology NYS Institute for Basic Research in Developmental Disabilities Staten Island New York USA.

Mark Mapstone (M)

Department of Neurology University of California Irvine California USA.

Wayne Silverman (W)

Department of Pediatrics School of Medicine University of California Irvine California USA.

Ira Lott (I)

Department of Pediatrics School of Medicine University of California Irvine California USA.

William Klunk (W)

Department of Psychiatry University of Pittsburgh Pittsburgh Pennsylvania USA.

Elizabeth Head (E)

Department of Pathology Gillespie Neuroscience Research Facility, University of California Irvine California USA.

Brad Christian (B)

Department of Medical Physics and Psychiatry University of Wisconsin Madison Madison Wisconsin USA.

Florence Lai (F)

Department of Neurology Massachusetts General Hospital Harvard Medical School Charlestown Massachusetts USA.

H Diana Rosas (HD)

Departments of Neurology and Radiology Massachusetts General Hospital Harvard Medical School Charlestown Massachusetts USA.

Shahid Zaman (S)

Department of Psychiatry School of Clinical Medicine University of Cambridge Cambridge UK.
Cambridgeshire and Peterborough NHS Foundation Trust Fulbourn Hospital Cambridge UK.

Melissa E Petersen (ME)

Department of Family Medicine and Institute for Translational Research University of North Texas Health Science Center Fort Worth Texas USA.

Andre Strydom (A)

Department of Forensic and Neurodevelopmental Sciences Institute of Psychiatry, Psychology and Neuroscience King's College London London UK.

Juan Fortea (J)

Sant Pau Memory Unit Department of Neurology Hospital de la Santa Creu i Sant Pau Biomedical Research Institute Sant Pau Universitat Autònoma de Barcelona Barcelona Spain.

Benjamin Handen (B)

Department of Psychiatry University of Pittsburgh Pittsburgh Pennsylvania USA.

Sid O'Bryant (S)

Institute for Translational Research and Department of Pharmacology and Neuroscience University of North Texas Health Science Center Fort Worth Texas USA.

Classifications MeSH