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Cognitive Reserve and Brain Reserve in Prodromal Huntington's Disease

Published online by Cambridge University Press:  23 May 2013

Aaron Bonner-Jackson ,
Jeffrey D. Long ,
Holly Westervelt ,
Geoffrey Tremont ,
Elizabeth Aylward ,
Jane S. Paulsen  and
The PREDICT-HD Investigators and Coordinators of the Huntington Study Group
Aaron Bonner-Jackson
Affiliation:
Cleveland Clinic, Cleveland, Ohio
Jeffrey D. Long
Affiliation:
University of Iowa, Iowa City, Iowa
Holly Westervelt
Affiliation:
Rhode Island Hospital, Providence, Rhode Island Alpert Medical School of Brown University, Providence, Rhode Island
Geoffrey Tremont
Affiliation:
Rhode Island Hospital, Providence, Rhode Island Alpert Medical School of Brown University, Providence, Rhode Island
Elizabeth Aylward
Affiliation:
Seattle Children's Research Institute, Seattle, Washington
Jane S. Paulsen*
Affiliation:
University of Iowa, Iowa City, Iowa
*
Correspondence and reprint requests to: Jane S. Paulsen, 500 Newton Road, 1-305 MEB, Iowa City, IA 52242. E-mail: [email protected]
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Abstract

Huntington disease (HD) is associated with decline in cognition and progressive morphological changes in brain structures. Cognitive reserve may represent a mechanism by which disease-related decline may be delayed or slowed. The current study examined the relationship between cognitive reserve and longitudinal change in cognitive functioning and brain volumes among prodromal (gene expansion-positive) HD individuals. Participants were genetically confirmed individuals with prodromal HD enrolled in the PREDICT-HD study. Cognitive reserve was computed as the composite of performance on a lexical task estimating premorbid intellectual level, occupational status, and years of education. Linear mixed effects regression (LMER) was used to examine longitudinal changes on four cognitive measures and three brain volumes over approximately 6 years. Higher cognitive reserve was significantly associated with a slower rate of change on one cognitive measure (Trail Making Test, Part B) and slower rate of volume loss in two brain structures (caudate, putamen) for those estimated to be closest to motor disease onset. This relationship was not observed among those estimated to be further from motor disease onset. Our findings demonstrate a relationship between cognitive reserve and both a measure of executive functioning and integrity of certain brain structures in prodromal HD individuals. (JINS, 2013, 19, 1–12).

Keywords

Huntington diseaseProdromalCognitive reserveCognitionCaudatePutamen
Type
Research Articles
Information
Journal of the International Neuropsychological Society , Volume 19 , Issue 7 , August 2013 , pp. 739 - 750
Copyright
Copyright © The International Neuropsychological Society 2013 

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