E019 Brain age as a new measure of disease stratification in Huntington’s disease

<h3></h3> Accurately characterizing progression states is crucial for developing effective therapeutic interventions. Various factors contribute to this challenge, including the need for precise methods that can account for the complex nature of HD progression. This study aims to address this gap by leveraging the concept of the brain’s biological age as a foundation for a data-driven clustering method to delineate various states of progression. Brain age, influenced by somatic expansion and its impact on brain volumes, offers a promising avenue for stratification, by stratifying subgroups and determining the optimal timing for interventions. To achieve this, data from 953 participants (including more than 5000 scans) across diverse cohorts, including PREDICT-HD, TRACK-HD, and IMAGE-HD, were analysed. Brain age was computed using Gaussian Processes Regression, with brain volumetric data as independent variable and age as dependent variable, and participants were categorized into four groups based on CAG and age product score. Unsupervised k-means clustering with brain-predicted age difference (brain-PAD) was then employed to identify distinct progression states. The analysis revealed significant disparities in brain age between HD participants and controls, with these differences becoming more pronounced as the disease progressed. Brain-PAD demonstrated a correlation with disease severity, effectively identifying five distinct progression states characterized by significant longitudinal disparities. These findings highlight the potential of brain-PAD in capturing HD progression states, thereby enhancing prognostic methodologies and providing valuable insights for future clinical trial designs and interventions.

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Published
2024-09-01
DOI
https://doi.org/10.1136/jnnp-2024-ehdn.115
Primary Topic
Genetic Neurodegenerative Diseases
Type
article
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article

E019 Brain age as a new measure of disease stratification in Huntington’s disease

James H. Cole, Nellie Georgiou‐Karistianis, Govinda Poudel, Jeffrey D. Long et al.
Genetic Neurodegenerative Diseases
article

E019 Brain age as a new measure of disease stratification in Huntington’s disease

James H. Cole, Nellie Georgiou‐Karistianis, Govinda Poudel, Jeffrey D. Long, Sarah J. Tabrizi, Adeel Razi, Jane S. Paulsen, Pubuditha M. Abeyasinghe
article en

Abstract

<h3></h3> Accurately characterizing progression states is crucial for developing effective therapeutic interventions. Various factors contribute to this challenge, including the need for precise methods that can account for the complex nature of HD progression. This study aims to address this gap by leveraging the concept of the brain’s biological age as a foundation for a data-driven clustering method to delineate various states of progression. Brain age, influenced by somatic expansion and its impact on brain volumes, offers a promising avenue for stratification, by stratifying subgroups and determining the optimal timing for interventions. To achieve this, data from 953 participants (including more than 5000 scans) across diverse cohorts, including PREDICT-HD, TRACK-HD, and IMAGE-HD, were analysed. Brain age was computed using Gaussian Processes Regression, with brain volumetric data as independent variable and age as dependent variable, and participants were categorized into four groups based on CAG and age product score. Unsupervised k-means clustering with brain-predicted age difference (brain-PAD) was then employed to identify distinct progression states. The analysis revealed significant disparities in brain age between HD participants and controls, with these differences becoming more pronounced as the disease progressed. Brain-PAD demonstrated a correlation with disease severity, effectively identifying five distinct progression states characterized by significant longitudinal disparities. These findings highlight the potential of brain-PAD in capturing HD progression states, thereby enhancing prognostic methodologies and providing valuable insights for future clinical trial designs and interventions.

University of Iowa (US), University of Wisconsin–Madison (US), Wellcome Centre for Human Neuroimaging (GB), Huntington's Disease Association (GB), UK Dementia Research Institute (GB), National Hospital for Neurology and Neurosurgery (GB), University College London (GB), Monash University (AU), Australian Catholic University (AU)
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Genetic Neurodegenerative Diseases
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