Beyond the average patient: how neuroimaging models can address heterogeneity in dementia

Author:

Verdi Serena12ORCID,Marquand Andre F34,Schott Jonathan M2ORCID,Cole James H12ORCID

Affiliation:

1. Centre for Medical Image Computing, Medical Physics and Biomedical Engineering, University College London, London WC1V 6LJ, UK

2. Dementia Research Centre, UCL Queen Square Institute of Neurology, London WC1N 3BG, UK

3. Donders Centre for Cognitive Neuroimaging, Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, 6525EN, The Netherlands

4. Department of Cognitive Neuroscience, Radboud University Medical Centre, Nijmegen, 6525EN, The Netherlands

Abstract

Abstract Dementia is a highly heterogeneous condition, with pronounced individual differences in age of onset, clinical presentation, progression rates and neuropathological hallmarks, even within a specific diagnostic group. However, the most common statistical designs used in dementia research studies and clinical trials overlook this heterogeneity, instead relying on comparisons of group average differences (e.g. patient versus control or treatment versus placebo), implicitly assuming within-group homogeneity. This one-size-fits-all approach potentially limits our understanding of dementia aetiology, hindering the identification of effective treatments. Neuroimaging has enabled the characterization of the average neuroanatomical substrates of dementias; however, the increasing availability of large open neuroimaging datasets provides the opportunity to examine patterns of neuroanatomical variability in individual patients. In this update, we outline the causes and consequences of heterogeneity in dementia and discuss recent research that aims to tackle heterogeneity directly, rather than assuming that dementia affects everyone in the same way. We introduce spatial normative modelling as an emerging data-driven technique, which can be applied to dementia data to model neuroanatomical variation, capturing individualized neurobiological ‘fingerprints’. Such methods have the potential to detect clinically relevant subtypes, track an individual’s disease progression or evaluate treatment responses, with the goal of moving towards precision medicine for dementia.

Funder

EPSRC

UCL Centre for Doctoral Training in Intelligent, Integrated Imaging in Healthcare

Department of Health’s National Institute for Health Research

University College London Hospitals Biomedical Research Centre

Dutch Organization for Scientific Research

Alzheimers Research UK

Brain Research UK

Weston Brain Institute, Medical Research Council

British Heart Foundation

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

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