Please use this identifier to cite or link to this item: http://ahro.austin.org.au/austinjspui/handle/1/18723
Title: Acceleration of hippocampal atrophy rates in asymptomatic amyloidosis.
Authors: Andrews, K Abigail;Frost, Chris;Modat, Marc;Cardoso, M Jorge;Rowe, Chris C;Villemagne, Victor;Fox, Nick C;Ourselin, Sebastien;Schott, Jonathan M
Affiliation: Dementia Research Centre, Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK
Centre for Medical Image Computing, UCL, London, UK
London School of Hygiene and Tropical Medicine, London, UK
Department of Nuclear Medicine & Centre for PET, Austin Health, Heidelberg, Victoria, Australia
Issue Date: Mar-2016
EDate: 2015-10-22
Citation: Neurobiology of aging 2016; 39: 99-107
Abstract: Increased rates of brain atrophy measured from serial magnetic resonance imaging precede symptom onset in Alzheimer's disease and may be useful outcome measures for prodromal clinical trials. Appropriate trial design requires a detailed understanding of the relationships between β-amyloid load and accumulation, and rate of brain change at this stage of the disease. Fifty-two healthy individuals (72.3 ± 6.9 years) from Australian Imaging, Biomarkers and Lifestyle Study of Aging had serial (0, 18 m, 36 m) magnetic resonance imaging, (0, 18 m) Pittsburgh compound B positron emission tomography, and clinical assessments. We calculated rates of whole brain and hippocampal atrophy, ventricular enlargement, amyloid accumulation, and cognitive decline. Over 3 years, rates of whole brain atrophy (p < 0.001), left and right hippocampal atrophy (p = 0.001, p = 0.023), and ventricular expansion (p < 0.001) were associated with baseline β-amyloid load. Whole brain atrophy rates were also independently associated with β-amyloid accumulation over the first 18 months (p = 0.003). Acceleration of left hippocampal atrophy rate was associated with baseline β-amyloid load across the cohort (p < 0.02). We provide evidence that rates of atrophy are associated with both baseline β-amyloid load and accumulation, and that there is presymptomatic, amyloid-mediated acceleration of hippocampal atrophy. Clinical trials using rate of hippocampal atrophy as an outcome measure should not assume linear decline in the presymptomatic phase.
URI: http://ahro.austin.org.au/austinjspui/handle/1/18723
DOI: 10.1016/j.neurobiolaging.2015.10.013
ORCID: 0000-0003-3910-2453
PubMed URL: 26923406
Type: Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Subjects: Acceleration
Asymptomatic amyloidosis
Atrophy
Hippocampus
MRI
PET
Appears in Collections:Journal articles

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