Discovery of disrupted sustained attention and altered functional connectivity in far‐from‐onset Huntington's disease gene‐expanded young adults
Christelle Langley, Michela Leocadi, Nicola Z. Hobbs, Mena Farag, Michael J. Murphy, Kate Fayer, Rachael I. Scahill, James B. Rowe, Trevor W. Robbins, Sarah J. Tabrizi, Barbara J. Sahakian

TL;DR
This study finds early attention problems and brain connectivity changes in young adults with the Huntington's disease gene, before motor symptoms appear.
Contribution
The study identifies sustained attention as an early cognitive biomarker in Huntington's disease gene carriers.
Findings
HD gene-expanded individuals showed significantly poorer sustained attention than controls.
Altered functional connectivity was observed in attention-related brain networks.
Attention deficits remained stable over a 4.7-year period in HD gene-expanded individuals.
Abstract
Cognitive impairments are a hallmark of Huntington's disease (HD). Seventy‐one participants (43 HD gene‐expanded [HDGE], 28 healthy controls) from the HD‐Young Adult Study at two timepoints ≈ 4.7 years apart, completed the Cambridge Neuropsychological Test Automated Battery Rapid Visual Information Processing task and underwent resting‐state functional magnetic resonance imaging. We focused on predefined regions of interest that are involved in sustained attention. HDGE individuals showed significantly poorer sustained attention than controls (padj = 0.007), with no significant change over time. Functional connectivity (FC) analyses revealed group differences in attention‐related networks, including the occipital–operculum and lentiform–orbitalis pathways. Time and group × time effects were also observed in frontal and parietal regions. These findings demonstrate early and…
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Taxonomy
TopicsGenetic Neurodegenerative Diseases · Functional Brain Connectivity Studies · Neurological disorders and treatments
