4.7 Article

Clusters of anatomical disease-burden patterns in ALS: a data-driven approach confirms radiological subtypes

Journal

JOURNAL OF NEUROLOGY
Volume 269, Issue 8, Pages 4404-4413

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00415-022-11081-3

Keywords

Amyotrophic lateral sclerosis; Neuroimaging; Biomarkers; Motor neuron disease; Diffusion imaging; Clinical trials

Funding

  1. IReL Consortium
  2. Health Research Board [HRB EIA-2017-019, HRB JPND-CoFund2-2019-1]
  3. Irish Institute of Clinical Neuroscience (IICN)
  4. Spastic Paraplegia Foundation (SPF)
  5. EU Joint Programme-Neurodegenerative Disease Research (JPND)
  6. Andrew Lydon scholarship
  7. Iris O'Brien Foundation

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This study conducted a prospective research using an imaging protocol to identify subtypes of amyotrophic lateral sclerosis (ALS) based on preferential cerebral involvement. Cluster analysis revealed two radiological clusters with different patterns of brain regions involvement. The hierarchy of anatomical regions in decreasing importance was also identified.
Amyotrophic lateral sclerosis (ALS) is associated with considerable clinical heterogeneity spanning from diverse disability profiles, differences in UMN/LMN involvement, divergent progression rates, to variability in frontotemporal dysfunction. A multitude of classification frameworks and staging systems have been proposed based on clinical and neuropsychological characteristics, but disease subtypes are seldom defined based on anatomical patterns of disease burden without a prior clinical stratification. A prospective research study was conducted with a uniform imaging protocol to ascertain disease subtypes based on preferential cerebral involvement. Fifteen brain regions were systematically evaluated in each participant based on a comprehensive panel of cortical, subcortical and white matter integrity metrics. Using min-max scaled composite regional integrity scores, a two-step cluster analysis was conducted. Two radiological clusters were identified; 35.5% of patients belonging to 'Cluster 1' and 64.5% of patients segregating to 'Cluster 2'. Subjects in Cluster 1 exhibited marked frontotemporal change. Predictor ranking revealed the following hierarchy of anatomical regions in decreasing importance: superior lateral temporal, inferior frontal, superior frontal, parietal, limbic, mesial inferior temporal, peri-Sylvian, subcortical, long association fibres, commissural, occipital, 'sensory', 'motor', cerebellum, and brainstem. While the majority of imaging studies first stratify patients based on clinical criteria or genetic profiles to describe phenotype- and genotype-associated imaging signatures, a data-driven approach may identify distinct disease subtypes without a priori patient categorisation. Our study illustrates that large radiology datasets may be potentially utilised to uncover disease subtypes associated with unique genetic, clinical or prognostic profiles.

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