Stepwise Functional Brain Architecture Correlates with Atrophy in Progressive Supranuclear Palsy

Author:

Spinelli Edoardo Gioele123,Ghirelli Alma123,Bottale Ilaria123,Basaia Silvia1ORCID,Canu Elisa1,Castelnovo Veronica1,Volontè Maria Antonietta3,Galantucci Sebastiano3,Magnani Giuseppe3,Caso Francesca3,Cecchetti Giordano134,Caroppo Paola5,Prioni Sara5,Villa Cristina5,Josephs Keith A.6,Whitwell Jennifer L.7,Filippi Massimo12348ORCID,Agosta Federica123ORCID

Affiliation:

1. Neuroimaging Research Unit, Division of Neuroscience IRCCS San Raffaele Scientific Institute Milan Italy

2. Vita‐Salute San Raffaele University Milan Italy

3. Neurology Unit, IRCCS San Raffaele Scientific Institute Milan Italy

4. Neurophysiology Service, IRCCS San Raffaele Scientific Institute Milan Italy

5. Unit of Neurology 5—Neuropathology, Fondazione IRCCS Istituto Neurologico Carlo Besta Milan Italy

6. Department of Neurology Mayo Clinic Rochester Minnesota USA

7. Department of Radiology Mayo Clinic Rochester Minnesota USA

8. Neurorehabilitation Unit, IRCCS San Raffaele Scientific Institute Milan Italy

Abstract

AbstractBackgroundStepwise functional connectivity (SFC) detects whole‐brain functional couplings of a selected region of interest at increasing link‐step topological distances.ObjectiveThis study applied SFC to test the hypothesis that stepwise architecture propagating from the disease epicenter would shape patterns of brain atrophy in patients with progressive supranuclear palsy–Richardson's syndrome (PSP‐RS).MethodsThirty‐six patients with PSP‐RS and 44 age‐matched healthy control subjects underwent brain magnetic resonance imaging on a 3‐T scanner. The disease epicenter was defined as the peak of atrophy observed in an independent cohort of 13 cases with postmortem confirmation of PSP pathology and used as seed region for SFC analysis. First, we explored SFC rearrangements in patients with PSP‐RS, as compared with age‐matched control subjects. Subsequently, we tested SFC architecture propagating from the disease epicenter as a determinant of brain atrophy distribution.ResultsThe disease epicenter was identified in the left midbrain tegmental region. Compared with age‐matched control subjects, patients with PSP‐RS showed progressively widespread decreased SFC of the midbrain with striatal and cerebellar regions through direct connections and sensorimotor cortical regions through indirect connections. A correlation was found between average link‐step distance from the left midbrain in healthy subjects and brain volumes in patients with PSP‐RS (r = 0.38, P < 0.001).ConclusionsThis study provides comprehensive insights into the topology of functional network rearrangements in PSP‐RS and demonstrates that the brain architectural topology, as described by SFC propagating from the disease epicenter, shapes the pattern of atrophic changes in PSP‐RS. Our findings support the view of a network‐based pathology propagation in this primary tauopathy. © 2024 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Funder

FP7 Ideas: European Research Council

European Commission

National Institutes of Health

Publisher

Wiley

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