Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/27048
Title: Pattern and degree of individual brain atrophy predicts dementia onset in dominantly inherited Alzheimer's disease.
Austin Authors: 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 ;Ghetti, Bernardino;Saykin, Andrew J;Jack, Clifford R;Graff-Radford, Neill R;Weiner, Michael;Cash, David M;Allegri, Ricardo F;Chrem, Patricio;Yi, Su;Miller, Bruce L;Rabinovici, Gil D;Rosen, Howard J
Affiliation: Department of Epidemiology and Biostatistics University of California San Francisco California USA
Department of Medicine University of California, San Francisco San Francisco California USA
Department of Psychiatry University of California, San Francisco San Francisco California USA
Department of Neurology University of California, San Francisco San Francisco California USA
Charles F. and Joanne Knight Alzheimer Disease Research Center, Department of Neurology Washington University School of Medicine St. Louis Missouri USA
Department of Neurology Washington University School of Medicine St. Louis Missouri USA
Department of Radiology Washington University School of Medicine St. Louis Missouri USA
Division of Neuropathology, Department of Pathology & Immunology Washington University School of Medicine St. Louis Missouri USA
Division of Biostatistics, Department of Psychiatry Washington University in St. Louis School of Medicine St. Louis Missouri USA
German Center for Neurodegenerative Diseases (DZNE) Munich Germany
Department of Neurology Ludwig-Maximilians-Universität München Munich Germany
Global Brain Health Institute University of California San Francisco California USA
Department of Neurology, Memory and Aging Center University of California San Francisco California USA
Alzheimer's Disease Research Center, Keck School of Medicine University of Southern California Los Angeles California USA
Warren Alpert Medical School Brown University Providence Rhode Island USA
Massachusetts General Hospital, Harvard Medical School Boston Boston Massachusetts USA
Taub Institute for Research on Alzheimer's Disease and the Aging Brain Columbia University New York New York USA
Dementia Research Centre, Department of Neurodegenerative Disease, UCL Queen Square Institute of Neurology University College London London UK
Centre for Medical Image Computing, Department of Medical Physics and Biomedical Engineering University College London London UK
Department of Biomedical Sciences Macquarie University North Ryde New South Wales Australia
Centre of Excellence for Alzheimer's Disease Research and Care, School of Medical and Health Sciences Edith Cowan University Joondalup Western Australia Australia
School of Psychiatry and Clinical Neurosciences University of Western Australia Crawley Western Australia Australia
Australian Alzheimer's Research Foundation Nedlands Western Australia Australia
The Cooperative Research Centre for Mental Health Carlton South Victoria Australia
Neuroscience Research Australia, Randwick Sydney New South Wales Australia
Prince of Wales Hospital Clinical School UNSW Sydney Sydney New South Wales Australia
Department of Molecular Imaging, Royal Prince Alfred Hospital, Sydney Medical School University of Sydney Camperdown New South Wales Australia
The Florey Institute University of Melbourne Parkville Victoria Australia
Department of Radiology Mayo Clinic Rochester Minnesota USA
Banner Alzheimer's Institute Phoenix Arizona USA
Molecular Imaging and Therapy
German Center for Neurodegenerative Diseases (DZNE) Tübingen Germany
Department of Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research University of Tübingen Tübingen Germany
Institute for Nuclear Medicine and Clinical Molecular Imaging Eberhard Karls University Tübingen Germany
School of Medical Sciences UNSW Sydney Sydney New South Wales Australia
Department of Pathology and Laboratory Medicine Indiana University School of Medicine Indianapolis Indiana USA
Department of Neurology Indiana University School of Medicine Indianapolis Indiana USA
Department of Radiology Indiana University School of Medicine Indianapolis Indiana USA
Department of Neurology Mayo Clinic Jacksonville Florida USA
Department of Veterans Affairs Medical Center Center for Imaging of Neurodegenerative Diseases San Francisco California USA
Department of Radiology University of California, San Francisco San Francisco California USA
Department of Cognitive Neurology, Neuropsychiatry and Neuropsychology Instituto de InvestigacionesNeurológicas FLENI Buenos Aires Argentina..
Issue Date: 5-Jul-2021
Date: 2021-07-05
Publication information: Alzheimer's & Dementia 2021; 13(1): e12197
Abstract: 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. 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. 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. Individualized risk scores based on brain atrophy could be useful for establishing enrollment criteria and stratifying DIAD-MC participants for prevention trials.
URI: https://ahro.austin.org.au/austinjspui/handle/1/27048
DOI: 10.1002/dad2.12197
Journal: Alzheimer's & Dementia
PubMed URL: 34258377
ISSN: 2352-8729
Type: Journal Article
Subjects: Dominantly Inherited Alzheimer Network
autosomal dominant Alzheimer's disease
brain atrophy
preclinical Alzheimer's disease
Appears in Collections:Journal articles

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