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Data-driven classification of cognitively normal and mild cognitive impairment subtypes predicts progression in the NACC dataset.
Edmonds, Emily C; Thomas, Kelsey R; Rapcsak, Steven Z; Lindemer, Shannon L; Delano-Wood, Lisa; Salmon, David P; Bondi, Mark W.
Afiliação
  • Edmonds EC; Banner Alzheimer's Institute, Tucson, Arizona, USA.
  • Thomas KR; Departments of Neurology and Psychology, University of Arizona, Tucson, Arizona, USA.
  • Rapcsak SZ; Research Service, Veterans Affairs San Diego Healthcare System, San Diego, California, USA.
  • Lindemer SL; Department of Psychiatry, University of California, San Diego, La Jolla, California, USA.
  • Delano-Wood L; Banner Alzheimer's Institute, Tucson, Arizona, USA.
  • Salmon DP; Departments of Neurology and Psychology, University of Arizona, Tucson, Arizona, USA.
  • Bondi MW; Department of Speech, Language, & Hearing Sciences, University of Arizona, Tucson, Arizona, USA.
Alzheimers Dement ; 20(5): 3442-3454, 2024 05.
Article em En | MEDLINE | ID: mdl-38574399
ABSTRACT

INTRODUCTION:

Data-driven neuropsychological methods can identify mild cognitive impairment (MCI) subtypes with stronger associations to dementia risk factors than conventional diagnostic methods.

METHODS:

Cluster analysis used neuropsychological data from participants without dementia (mean age = 71.6 years) in the National Alzheimer's Coordinating Center (NACC) Uniform Data Set (n = 26,255) and the "normal cognition" subsample (n = 16,005). Survival analyses examined MCI or dementia progression.

RESULTS:

Five clusters were identified "Optimal" cognitively normal (oCN; 13.2%), "Typical" CN (tCN; 28.0%), Amnestic MCI (aMCI; 25.3%), Mixed MCI-Mild (mMCI-Mild; 20.4%), and Mixed MCI-Severe (mMCI-Severe; 13.0%). Progression to dementia differed across clusters (oCN < tCN < aMCI < mMCI-Mild < mMCI-Severe). Cluster analysis identified more MCI cases than consensus diagnosis. In the "normal cognition" subsample, five clusters emerged High-All Domains (High-All; 16.7%), Low-Attention/Working Memory (Low-WM; 22.1%), Low-Memory (36.3%), Amnestic MCI (16.7%), and Non-amnestic MCI (naMCI; 8.3%), with differing progression rates (High-All < Low-WM = Low-Memory < aMCI < naMCI).

DISCUSSION:

Our data-driven methods outperformed consensus diagnosis by providing more precise information about progression risk and revealing heterogeneity in cognition and progression risk within the NACC "normal cognition" group.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Progressão da Doença / Disfunção Cognitiva / Testes Neuropsicológicos Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Progressão da Doença / Disfunção Cognitiva / Testes Neuropsicológicos Idioma: En Ano de publicação: 2024 Tipo de documento: Article