Searching for just a few words should be enough to get started. If you need to make more complex queries, use the tips below to guide you.
Article type: Research Article
Authors: Ciarochi, Jennifer A.a; * | Johnson, Hans J.b | Calhoun, Vince D.c; d | Liu, Jingyuc | Espinoza, Flor A.c | Bockholt, Henry J.c | Misiura, Mariae | Caprihan, Arvindc | Plis, Sergeyc | Paulsen, Jane S.f; g | Turner, Jessica A.a; e | the PREDICT-HD Investigators and Coordinators of the Huntington Study Group
Affiliations: [a] Neuroscience Institute, Georgia State University, Atlanta, GA, USA | [b] Department of Electrical and Computer Engineering, 1402 Seamans Center for the Engineering Arts and Science, The University of Iowa, Iowa City, IA, USA | [c] The Mind Research Network, Albuquerque, NM, USA | [d] Department of Electrical and Computer Engineering, University of New Mexico, Albuquerque, NM, USA | [e] Department of Psychology, Georgia State University, Atlanta, GA, USA | [f] Department of Psychiatry, Iowa Mental Health Clinical Research Center, University of Iowa, IA, USA | [g] Departments of Neurology and Psychology, University of Iowa, IA, USA
Correspondence: [*] Correspondence to: Jennifer Ciarochi, Neuroscience Institute, Georgia State University, Atlanta, GA 30302, USA. Tel.: +1 678 822 1847; E-mail: [email protected].
Abstract: Background:Gray matter (GM) atrophy in the striatum and across the brain is a consistently reported feature of the Huntington Disease (HD) prodrome. More recently, widespread prodromal white matter (WM) degradation has also been detected. However, longitudinal WM studies are limited and conflicting, and most analyses comparing WM and clinical functioning have also been cross-sectional. Objective:We simultaneously assessed changes in WM and cognitive and motor functioning at various prodromal HD stages. Methods:Data from 1,336 (1,047 prodromal, 289 control) PREDICT-HD participants were analyzed (3,700 sessions). MRI images were used to create GM, WM, and cerebrospinal fluid probability maps. Using source-based morphometry, independent component analysis was applied to WM probability maps to extract covarying spatial patterns and their subject profiles. WM profiles were analyzed in two sets of linear mixed model (LMM) analyses: one to compare WM profiles across groups cross-sectionally and longitudinally, and one to concurrently compare WM profiles and clinical variables cross-sectionally and longitudinally within each group. Results:Findings illustrate widespread prodromal changes in GM-adjacent-WM, with premotor, supplementary motor, middle frontal and striatal changes early in the prodrome that subsequently extend sub-gyrally with progression. Motor functioning agreed most with WM until the near-onset prodromal stage, when Stroop interference was the best WM indicator. Across groups, Trail-Making Test part A outperformed other cognitive variables in its similarity to WM, particularly cross-sectionally. Conclusions:Results suggest that distinct regions coincide with cognitive compared to motor functioning. Furthermore, at different prodromal stages, distinct regions appear to align best with clinical functioning. Thus, the informativeness of clinical measures may vary according to the type of data available (cross-sectional or longitudinal) as well as age and CAG-number.
Keywords: Cognition, magnetic resonance imaging, movement, multivariate analysis, prodromal symptoms, white matter
DOI: 10.3233/JHD-180332
Journal: Journal of Huntington's Disease, vol. 8, no. 2, pp. 199-219, 2019
IOS Press, Inc.
6751 Tepper Drive
Clifton, VA 20124
USA
Tel: +1 703 830 6300
Fax: +1 703 830 2300
[email protected]
For editorial issues, like the status of your submitted paper or proposals, write to [email protected]
IOS Press
Nieuwe Hemweg 6B
1013 BG Amsterdam
The Netherlands
Tel: +31 20 688 3355
Fax: +31 20 687 0091
[email protected]
For editorial issues, permissions, book requests, submissions and proceedings, contact the Amsterdam office [email protected]
Inspirees International (China Office)
Ciyunsi Beili 207(CapitaLand), Bld 1, 7-901
100025, Beijing
China
Free service line: 400 661 8717
Fax: +86 10 8446 7947
[email protected]
For editorial issues, like the status of your submitted paper or proposals, write to [email protected]
如果您在出版方面需要帮助或有任何建, 件至: [email protected]