作者
Vincent Planche,Vincent Bouteloup,Jean-François Mangin,Bruno Dubois,J. Delrieu,Florence Pasquier,Frédéric Blanc,Claire Paquet,Olivier Hanon,Audrey Gabelle,Matthieu Ceccaldi,Cédric Annweiler,Pierre Krolak-Salmon,Marie-Odile Habert,Clara Fischer,Marie Chupin,Yannick Béjot,Olivier Godefroy,David Wallon,Mathilde Sauvée,Isabelle Bourdel-Marchasson,Isabelle Jalenques,François Tison,Geneviève Chêne,Carole Dufouil
摘要
Introduction The clinical relevance of brain atrophy subtypes categorization in non-demented persons without a priori knowledge regarding their amyloid status or clinical presentation is unknown. Methods A total of 2083 outpatients with either subjective cognitive complaint or mild cognitive impairment at study entry were followed during 4 years (MEMENTO cohort). Atrophy subtypes were defined using baseline magnetic resonance imaging (MRI) and previously described algorithms. Results Typical/diffuse atrophy was associated with faster cognitive decline and the highest risk of developing dementia and Alzheimer's disease (AD) over time, both in the whole analytic sample and in amyloid-positive participants. Hippocampal-sparing and limbic-predominant atrophy were also associated with incident dementia, with faster cognitive decline in the limbic predominant atrophy group. Lewy body dementia was more frequent in the hippocampal-sparing and minimal/no atrophy groups. Discussion Atrophy subtypes categorization predicted different subsequent patterns of cognitive decline and rates of conversion to distinct etiologies of dementia in persons attending memory clinics.