Stepwise Functional Brain Architecture Correlates with Atrophy in Progressive Supranuclear Palsy

• Published in: Movement disorders Vol. 39; no. 9; pp. 1493 - 1503
• Main Authors: Spinelli, Edoardo Gioele, Ghirelli, Alma, Bottale, Ilaria, Basaia, Silvia, Canu, Elisa, Castelnovo, Veronica, Volontè, Maria Antonietta, Galantucci, Sebastiano, Magnani, Giuseppe, Caso, Francesca, Cecchetti, Giordano, Caroppo, Paola, Prioni, Sara, Villa, Cristina, Josephs, Keith A., Whitwell, Jennifer L., Filippi, Massimo, Agosta, Federica
• Format: Journal Article
• Language: English
• Published: Hoboken, USA John Wiley & Sons, Inc 01.09.2024; Wiley Subscription Services, Inc
• Subjects: Age composition; Aged; Atrophy; Atrophy - pathology; Brain - diagnostic imaging; Brain - pathology; Brain architecture; Cerebellum; Female; Humans; Image processing; Magnetic Resonance Imaging; Male; Mesencephalon; Middle Aged; Movement disorders; MRI; Neostriatum; Neural networks; Neurodegenerative diseases; Neuroimaging; Pathology; Progressive supranuclear palsy; resting‐state functional MRI; RS fMRI; Sensorimotor system; SFC; stepwise functional connectivity; Supranuclear Palsy, Progressive - diagnostic imaging; Supranuclear Palsy, Progressive - pathology; Tau protein; SFC; stepwise functional connectivity; resting‐state functional MRI; MRI; RS fMRI; progressive supranuclear palsy
• ISSN: 0885-3185; 1531-8257; 1531-8257
• DOI: 10.1002/mds.29887

Background Stepwise functional connectivity (SFC) detects whole‐brain functional couplings of a selected region of interest at increasing link‐step topological distances. Objective This 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). Methods Thirty‐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. Results The 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). Conclusions This 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.