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Longitudinal whole-brain atrophy and ventricular enlargement in nondemented Parkinson's disease

Authors :
Michael J. Firbank
Tien K. Khoo
Brit Mollenhauer
Elijah Mak
Rachael A Lawson
David J. Burn
James B. Rowe
Guy B. Williams
Alison J. Yarnall
John T. O'Brien
David J. Brooks
Roger A. Barker
Gordon W Duncan
Adrian M. Owen
Li Su
Mak, Elijah [0000-0002-6437-8024]
Williams, Guy [0000-0001-5223-6654]
Rowe, James [0000-0001-7216-8679]
Barker, Roger [0000-0001-8843-7730]
O'Brien, John [0000-0002-0837-5080]
Apollo - University of Cambridge Repository
Source :
Mak, E, Su, L, Williams, G B, Firbank, M J, Lawson, R A, Yarnall, A J, Duncan, G W, Mollenhauer, B, Owen, A M, Khoo, T K, Brooks, D J, Rowe, J B, Barker, R A, Burn, D J & O'Brien, J T 2017, ' Longitudinal whole-brain atrophy and ventricular enlargement in nondemented Parkinson's disease ', Neurobiology of Aging, vol. 55, pp. 78-90 . https://doi.org/10.1016/j.neurobiolaging.2017.03.012, Brain and Mind Institute Researchers' Publications, Neurobiology of Aging
Publication Year :
2017
Publisher :
Elsevier BV, 2017.

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.

Details

ISSN :
01974580
Volume :
55
Database :
OpenAIRE
Journal :
Neurobiology of Aging
Accession number :
edsair.doi.dedup.....dda41e734ca4b85e4540b5743a77b335
Full Text :
https://doi.org/10.1016/j.neurobiolaging.2017.03.012