Functional magnetic resonance imaging of working memory in Huntington's disease: cross-sectional data from the IMAGE-HD study

Nellie Georgiou-Karistianis, Julie C Stout, Juan F Dominguez, Sarah-Pia Carron, Ayaka Ando, Andrew J Churchyard, Phyllis Chua, India Kate Bohanna, Alicia Rhian Dymowski, Govinda Poudel, Gary Francis Egan

Research output: Contribution to journalArticleResearchpeer-review

44 Citations (Scopus)

Abstract

We used functional magnetic resonance imaging (fMRI) to investigate spatial working memory (WM) in an N-BACK task (0, 1, and 2-BACK) in premanifest Huntington s disease (pre-HD, n = 35), early symptomatic Huntington s disease (symp-HD, n = 23), and control (n = 32) individuals. Overall, both WM conditions (1-BACK and 2-BACK) activated a large network of regions throughout the brain, common to all groups. However, voxel-wise and time-course analyses revealed significant functional group differences, despite no significant behavioral performance differences. During 1-BACK, voxel-wise blood-oxygen-level-dependent (BOLD) signal activity was significantly reduced in a number of regions from the WM network (inferior frontal gyrus, anterior insula, caudate, putamen, and cerebellum) in pre-HD and symp-HD groups, compared with controls; however, time-course analysis of the BOLD response in the dorsolateral prefrontal cortex (DLPFC) showed increased activation in symp-HD, compared with pre-HD and controls. The pattern of reduced voxel-wise BOLD activity in pre-HD and symp-HD, relative to controls, became more pervasive during 2-BACK affecting the same structures as in 1-BACK, but also incorporated further WM regions (anterior cingulate gyrus, parietal lobe and thalamus). The DLPFC BOLD time-course for 2-BACK showed a reversed pattern to that observed in 1-BACK, with a significantly diminished signal in symp-HD, relative to pre-HD and controls. Our findings provide support for functional brain reorganisation in cortical and subcortical regions in both pre-HD and symp-HD, which are modulated by task difficulty. Moreover, the lack of a robust striatal BOLD signal in pre-HD may represent a very early signature of change observed up to 15 years prior to clinical diagnosis.
Original languageEnglish
Pages (from-to)1847 - 1864
Number of pages18
JournalHuman Brain Mapping
Volume35
Issue number5
DOIs
Publication statusPublished - 2014

Cite this