Structural and metabolic brain correlates of arithmetic word‐problem solving in Huntington's disease

Author:

Horta‐Barba Andrea12345ORCID,Martinez‐Horta Saul12345ORCID,Sampedro Frederic123ORCID,Pérez‐Pérez Jesús12345ORCID,Camacho Valle6ORCID,Pagonabarraga Javier12345ORCID,Kulisevsky Jaime12345ORCID

Affiliation:

1. Movement Disorders Unit, Neurology Department Hospital de la Santa Creu i Sant Pau Barcelona Spain

2. Biomedical Research Institute (IIB‐Sant Pau) Barcelona Spain

3. Centro de Investigación en Red‐Enfermedades Neurodegenerativas (CIBERNED) Madrid Spain

4. Department of Medicine Autonomous University of Barcelona (UAB) Bellaterra Spain

5. European Huntington's Disease Network (EHDN) Bellaterra Spain

6. Department of Nuclear Medicine Santa Creu i Sant Pau Hospital Barcelona Spain

Abstract

AbstractIndividuals with pre‐manifest and early symptomatic Huntington's disease (HD) have shown deficits in solving arithmetic word‐problems. However, the neural correlates of these deficits in HD are poorly understood. We explored the structural (gray‐matter volume; GMV) and metabolic (18F‐FDG PET; SUVr) brain correlates of arithmetic performance using the recently developed HD‐word problem arithmetic task (HD‐WPA) in seventeen preHD and sixteen HD individuals. Symptomatic participants showed significantly lower scores in the HD‐WPA than preHD participants. Lower performance in the HD‐WPA was associated with reduced GMV in subcortical, medial frontal, and several posterior‐cortical clusters in HD participants. No significant GMV loss was found in preHD participants. 18F‐FDG data revealed a widespread pattern of hypometabolism in association with lower arithmetic performance in all participants. In preHD participants, this pattern was restricted to the ventrolateral and orbital prefrontal cortex, the insula, and the precentral gyrus. In HD participants, the pattern extended to several parietal–temporal regions. Word‐problem solving arithmetic deficits in HD is subserved by a pattern of asynchronous metabolic and structural compromise across the cerebral cortex as a function of disease stage. In preHD individuals, arithmetic deficits were associated with prefrontal alterations, whereas in symptomatic HD patients, more severe arithmetic deficits are associated with the compromise of several frontal‐subcortical and temporo‐parietal regions. Our results support the hypothesis that cognitive deficits in HD are not exclusively dominated by frontal‐striatal dysfunctions but also involve fronto‐temporal and parieto‐occipital damage.

Funder

Huntington's Disease Society of America

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience

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