Artículo

Pattern and degree of individual brain atrophy predicts dementia onset in dominantly inherited Alzheimer's disease

Keret, Ophir ; Staffaroni, Adam M. ; Ringman, John M. ; Cobigo, Yann ; Goh, Sheng Yang M. ; Wolf, Amy ; Allen, Isabel Elaine ; Salloway, Stephen ; Chhatwal, Jasmeer ; Brickman, Adam M. ; Reyes Dumeyer, Dolly ; Bateman, Randal J. ; Benzinger, Tammie L.S. ; Morris, John C. ; Ances, Beau M. ; Joseph Mathurin, Nelly ; Perrin, Richard J. ; Gordon, Brian A. ; Levin, Johannes ; Vöglein, Jonathan ; Jucker, Mathias ; la Fougère, Christian ; Martins, Ralph N. ; Sohrabi, Hamid R. ; Taddei, Kevin ; Villemagne, Victor L. ; Schofield, Peter R. ; Brooks, William S. ; Fulham, Michael ; Masters, Colin L. ; Allegri, Ricardo Francisco Icon

Otros responsables

Fecha

06/2021

Editorial

John Wiley & Sons

Revista

Alzheimers & Dementia

Título del libro

Nombre del evento

Fecha del evento

Institución organizadora

ISSN

1552-5260

eISSN

2352-8729

ISBN

Idioma

Inglés

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Clasificación temática

Resumen

Introduction: Asymptomatic and mildly symptomatic dominantly inherited Alzheimer's disease mutation carriers (DIAD-MC) are ideal candidates for preventative treatment trials aimed at delaying or preventing dementia onset. Brain atrophy is an early feature of DIAD-MC and could help predict risk for dementia during trial enrollment. Methods: We created a dementia risk score by entering standardized gray-matter volumes from 231 DIAD-MC into a logistic regression to classify participants with and without dementia. The score's predictive utility was assessed using Cox models and receiver operating curves on a separate group of 65 DIAD-MC followed longitudinally. Results: Our risk score separated asymptomatic versus demented DIAD-MC with 96.4% (standard error = 0.02) and predicted conversion to dementia at next visit (hazard ratio = 1.32, 95% confidence interval [CI: 1.15, 1.49]) and within 2 years (area under the curve = 90.3%, 95% CI [82.3%–98.2%]) and improved prediction beyond established methods based on familial age of onset. Discussion: Individualized risk scores based on brain atrophy could be useful for establishing enrollment criteria and stratifying DIAD-MC participants for prevention trials.

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