Titre | Clinical relevance of brain atrophy subtypes categorization in memory clinics. |
Publication Type | Journal Article |
Year of Publication | 2021 |
Authors | Planche V, Bouteloup V, Mangin J-F, Dubois B, Delrieu J, Pasquier F, Blanc F, Paquet C, Hanon O, Gabelle A, Ceccaldi M, Annweiler C, Krolak-Salmon P, Habert M-O, Fischer C, Chupin M, Béjot Y, Godefroy O, Wallon D, Sauvee M, Bourdel-Marchasson I, Jalenques I, Tison F, Chêne G, Dufouil C |
Corporate Authors | the MEMENTO Study group. |
Journal | Alzheimers Dement |
Volume | 17 |
Issue | 4 |
Pagination | 641-652 |
Date Published | 2021 04 |
ISSN | 1552-5279 |
Mots-clés | Aged, Alzheimer Disease, Ambulatory Care Facilities, Atrophy, Brain, Cohort Studies, Female, Hippocampus, Humans, Magnetic Resonance Imaging, Male, Memory Disorders |
Résumé | 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. |
DOI | 10.1002/alz.12231 |
Alternate Journal | Alzheimers Dement |
PubMed ID | 33325121 |