Deciphering the clinico-radiological heterogeneity of dysexecutive Alzheimer’s disease

Author:

Corriveau-Lecavalier Nick1,Barnard Leland R1,Lee Jeyeon2,Dicks Ellen1,Botha Hugo1,Graff-Radford Jonathan1,Machulda Mary M3,Boeve Bradley F1,Knopman David S1,Lowe Val J2,Petersen Ronald C1,Jack, Jr Clifford R2,Jones David T12ORCID

Affiliation:

1. Department of Neurology, Mayo Clinic , Rochester, MN 55905 , USA

2. Department of Radiology, Mayo Clinic , Rochester, MN 55905 , USA

3. Department of Psychiatry and Psychology, Mayo Clinic , Rochester, MN 55905 , USA

Abstract

Abstract Dysexecutive Alzheimer’s disease (dAD) manifests as a progressive dysexecutive syndrome without prominent behavioral features, and previous studies suggest clinico-radiological heterogeneity within this syndrome. We uncovered this heterogeneity using unsupervised machine learning in 52 dAD patients with multimodal imaging and cognitive data. A spectral decomposition of covariance between FDG-PET images yielded six latent factors (“eigenbrains”) accounting for 48% of variance in patterns of hypometabolism. These eigenbrains differentially related to age at onset, clinical severity, and cognitive performance. A hierarchical clustering on the eigenvalues of these eigenbrains yielded four dAD subtypes, i.e. “left-dominant,” “right-dominant,” “bi-parietal-dominant,” and “heteromodal-diffuse.” Patterns of FDG-PET hypometabolism overlapped with those of tau-PET distribution and MRI neurodegeneration for each subtype, whereas patterns of amyloid deposition were similar across subtypes. Subtypes differed in age at onset and clinical severity where the heteromodal-diffuse exhibited a worse clinical picture, and the bi-parietal had a milder clinical presentation. We propose a conceptual framework of executive components based on the clinico-radiological associations observed in dAD. We demonstrate that patients with dAD, despite sharing core clinical features, are diagnosed with variability in their clinical and neuroimaging profiles. Our findings support the use of data-driven approaches to delineate brain–behavior relationships relevant to clinical practice and disease physiology.

Funder

National Institutes of Health

Robert Wood Johnson Foundation

The Elsie and Marvin Dekelboum Family Foundation

The Liston Family Foundation

the Edson Family

The GHR Foundation

Foundation Dr Corinne Schuler

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Cognitive Neuroscience

Reference114 articles.

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