Longitudinal whole-brain atrophy and ventricular enlargement in nondemented Parkinson's disease
Authors
Su, Li
Firbank, MJ
Lawson, RA
Yarnall, AJ
Duncan, GW
Mollenhauer, B
Owen, AM
Khoo, TK
Brooks, DJ
Burn, DJ
Publication Date
2017-07-01Journal Title
Neurobiology of Aging
ISSN
0197-4580
Publisher
Elsevier BV
Volume
55
Pages
78-90
Language
English
Type
Article
This Version
VoR
Metadata
Show full item recordCitation
Mak, E., Su, L., Williams, G., Firbank, M., Lawson, R., Yarnall, A., Duncan, G., et al. (2017). Longitudinal whole-brain atrophy and ventricular enlargement in nondemented Parkinson's disease. Neurobiology of Aging, 55 78-90. https://doi.org/10.1016/j.neurobiolaging.2017.03.012
Abstract
We investigated whole-brain atrophy and ventricular enlargement over 18 months in nondemented Parkinson's disease (PD) and examined their associations with clinical measures and baseline CSF markers. PD subjects (n = 100) were classified at baseline into those with mild cognitive impairment (MCI; PD-MCI, n = 36) and no cognitive impairment (PD-NC, n = 64). Percentage of whole-brain volume change (PBVC) and ventricular expansion over 18 months were assessed with FSL-SIENA and ventricular enlargement (VIENA) respectively. PD-MCI showed increased global atrophy (-1.1% ± 0.8%) and ventricular enlargement (6.9 % ± 5.2%) compared with both PD-NC (PBVC: -0.4 ± 0.5, p < 0.01; VIENA: 2.1% ± 4.3%, p < 0.01) and healthy controls. In a subset of 35 PD subjects, CSF levels of tau, and Aβ42/Aβ40 ratio were correlated with PBVC and ventricular enlargement respectively. The sample size required to demonstrate a 20% reduction in PBVC and VIENA was approximately 1/15th of that required to detect equivalent changes in cognitive decline. These findings suggest that longitudinal MRI measurements have potential to serve as surrogate markers to complement clinical assessments for future disease-modifying trials in PD.
Keywords
dementia, imaging, longitudinal, MRI, neurodegeneration, Parkinson's disease
Sponsorship
This study was funded by a Parkinson's UK grant (J-0802) and supported by Parkinson's UK (CN), Lockhart Parkinson's Disease Research Fund (RAL, TKK, GWD), Michael J. Fox Foundation (AJY), the National Institute for Health Research (NIHR, RG64473) Cambridge Biomedical Research Centre, and Biomedical Research Unit in Dementia, the Wellcome Trust (JBR, 103838); the Medical Research Council of Cognition, and Brain Sciences Unit, Cambridge (JBR, MC-A060-5PQ30); the NIHR Newcastle Biomedical Research Unit based at Newcastle-upon-Tyne Hospitals NHS Foundation Trust and Newcastle University; the NIHR Dementia and Neurodegenerative Diseases Research Network (JTO), and Elijah Mak was in receipt of the Gates Cambridge studentship and Alzheimer's Research UK scholarship.
Funder references
WELLCOME TRUST (103838/Z/14/Z)
Cambridge University Hospitals NHS Foundation Trust (CUH) (146281)
MEDICAL RESEARCH COUNCIL (MR/M009041/1)
Medical Research Council (MC_U105597119)
MEDICAL RESEARCH COUNCIL (MR/M024873/1)
Embargo Lift Date
2100-01-01
Identifiers
External DOI: https://doi.org/10.1016/j.neurobiolaging.2017.03.012
This record's URL: https://www.repository.cam.ac.uk/handle/1810/264452
Rights
Attribution 4.0 International, Attribution 4.0 International, Attribution 4.0 International, Attribution 4.0 International