# Discovery of disrupted sustained attention and altered functional connectivity in far‐from‐onset Huntington's disease gene‐expanded young adults

**Authors:** 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

PMC · DOI: 10.1002/alz.70944 · 2026-01-13

## 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.

## Key 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 persistent attention deficits in HDGE, linked to altered FC in attention‐related circuits. This supports the presence of early cognitive dysfunction in HD and highlights potential compensatory and pathological changes in brain networks prior to the onset of clinical motor symptoms.

We detail the discovery of early sustained attention deficits in Huntington's disease (HD) gene‐expanded (HDGE) young adults.These sustained attention deficits do not measurably decline over a 4.7‐year period.Altered functional connectivity was observed in attention‐related brain networks.Alterations in regions include occipital, opercular, lentiform, and frontal areas.Findings support attention as an early cognitive biomarker in HDGE young adults.

We detail the discovery of early sustained attention deficits in Huntington's disease (HD) gene‐expanded (HDGE) young adults.

These sustained attention deficits do not measurably decline over a 4.7‐year period.

Altered functional connectivity was observed in attention‐related brain networks.

Alterations in regions include occipital, opercular, lentiform, and frontal areas.

Findings support attention as an early cognitive biomarker in HDGE young adults.

## Linked entities

- **Diseases:** Huntington's disease (MONDO:0007739)

## Full-text entities

- **Genes:** HTT (huntingtin) [NCBI Gene 3064] {aka HD, IT15, LOMARS}
- **Diseases:** attention deficit hyperactivity disorder (MESH:D001289), ISS (MESH:C564479), neurodevelopmental disorder (MESH:D002658), psychiatric (MESH:D001523), inherited neurodegenerative disorder (MESH:D020271), inattention (MESH:D001308), neurodegeneration (MESH:D019636), motor abnormalities (MESH:D000014), hyperactivity (MESH:D006948), cognitive deficits (MESH:D003072), RESEARCH (MESH:D014947), neurodevelopmental deficit (MESH:D009461), movement, cognitive, and psychiatric symptoms (MESH:D019954), HD (MESH:D006816), sustained (MESH:D009120), disrupted (MESH:D019958), motor dysfunction (MESH:D000068079), impulsivity (MESH:D007174), CAG (MESH:C538228)
- **Chemicals:** CAG (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12797252/full.md

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Source: https://tomesphere.com/paper/PMC12797252