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Evaluating the Effect of Alzheimer's Disease‐Related Biomarker Change in Corticobasal Syndrome and Progressive Supranuclear Palsy

Indira García‐Cordero, Chloe Anastassiadis, Abeer Khoja, Alonso Morales‐Rivero, Simrika Thapa, Anna Vasilevskaya, Carly Davenport, Vishaal Sumra, Blas Couto, Namita Multani, Foad Taghdiri, Cassandra Jessica Anor, Karen Misquitta, Lawren VandeVrede, Hilary W. Heuer, David F. Tang‐Wai, Bradford Dickerson, Alexander Pantelyat, Irene Litvan, Bradley F. Boeve, Julio C. Rojas, Peter A. Ljubenkov, Edward D. Huey, Susan H. Fox, Gábor G. Kovács, Adam L. Boxer, Anthony E. Lang, Maria Carmela Tartaglia

2024Annals of Neurology18 citationsDOIOpen Access PDF

Abstract

OBJECTIVES: To evaluate the effect of Alzheimer's disease (AD) -related biomarker change on clinical features, brain atrophy and functional connectivity of patients with corticobasal syndrome (CBS) and progressive supranuclear palsy (PSP). METHODS: Data from patients with a clinical diagnosis of CBS, PSP, and AD and healthy controls were obtained from the 4-R-Tauopathy Neuroimaging Initiative 1 and 2, the Alzheimer's Disease Neuroimaging Initiative, and a local cohort from the Toronto Western Hospital. Patients with CBS and PSP were divided into AD-positive (CBS/PSP-AD) and AD-negative (CBS/PSP-noAD) groups based on fluid biomarkers and amyloid PET scans. Cognitive, motor, and depression scores; AD fluid biomarkers (cerebrospinal p-tau, t-tau, and amyloid-beta, and plasma ptau-217); and neuroimaging data (amyloid PET, MRI and fMRI) were collected. Clinical features, whole-brain gray matter volume and functional networks connectivity were compared across groups. RESULTS: Data were analyzed from 87 CBS/PSP-noAD and 23 CBS/PSP-AD, 18 AD, and 30 healthy controls. CBS/PSP-noAD showed worse performance in comparison to CBS/PSP-AD in the PSPRS [mean(SD): 34.8(15.8) vs 23.3(11.6)] and the UPDRS scores [mean(SD): 34.2(17.0) vs 21.8(13.3)]. CBS/PSP-AD demonstrated atrophy in AD signature areas and brainstem, while CBS/PSP-noAD patients displayed atrophy in frontal and temporal areas, globus pallidus, and brainstem compared to healthy controls. The default mode network showed greatest disconnection in CBS/PSP-AD compared with CBS/PSP-no AD and controls. The thalamic network connectivity was most affected in CBS/PSP-noAD. INTERPRETATION: AD biomarker positivity may modulate the clinical presentation of CBS/PSP, with evidence of distinctive structural and functional brain changes associated with the AD pathology/co-pathology. ANN NEUROL 2024;96:99-109.

Topics & Concepts

Progressive supranuclear palsyAtrophyBiomarkerNeuroimagingTauopathyCorticobasal degenerationMedicinePsychologyAlzheimer's diseasePathologyInternal medicineNeuroscienceDiseaseNeurodegenerationBiologyBiochemistryParkinson's Disease Mechanisms and TreatmentsNeurological disorders and treatmentsFunctional Brain Connectivity Studies