4.6 Article

Crossed cerebellar diaschisis on 18F-FDG PET: Frequency across neurodegenerative syndromes and association with 11C-PIB and 18F-Flortaucipir

Journal

JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM
Volume 41, Issue 9, Pages 2329-2343

Publisher

SAGE PUBLICATIONS INC
DOI: 10.1177/0271678X211001216

Keywords

Alzheimer's; diaschisis; FDG; PET; Tau

Funding

  1. National Institute on Aging [R01-AG-045611, P30-AG062422, P01-AG19724, K99AG065501]
  2. Rainwater Charitable Foundation (Tau Consortium)
  3. Alzheimer's Association [AARF-16-443577]
  4. State of California Department of Health Services Alzheimer's Disease Research Centre of California grant [04-33516]

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The study found a high frequency of CCD in patients with neurodegenerative diseases and its association with neuropathology. Cortical asymmetry may contribute to cerebellar metabolic imbalance in some patients, increasing the likelihood of CCD occurrence.
We used F-18-FDG-PET to investigate the frequency of crossed cerebellar diaschisis (CCD) in 197 patients with various syndromes associated with neurodegenerative diseases. In a subset of 117 patients, we studied relationships between CCD and cortical asymmetry of Alzheimer's pathology (beta-amyloid (C-11-PIB) and tau (F-18-Flortaucipir)). PET images were processed using MRIs to derive parametric SUVR images and define regions of interest. Indices of asymmetry were calculated in the cerebral cortex, basal ganglia and cerebellar cortex. Across all patients, cerebellar F-18-FDG asymmetry was associated with reverse asymmetry of F-18-FDG in the cerebral cortex (especially frontal and parietal areas) and basal ganglia. Based on our operational definition (cerebellar asymmetry >3% with contralateral supratentorial hypometabolism), significant CCD was present in 47/197 (24%) patients and was most frequent in corticobasal syndrome and semantic and logopenic variants of primary progressive aphasia. In beta-amyloid-positive patients, mediation analyses showed that F-18-Flortaucipir cortical asymmetry was associated with cerebellar F-18-FDG asymmetry, but that cortical F-18-FDG asymmetry mediated this relationship. Analysis of F-18-FDG-SUVR values suggested that CCD might also occur in the absence of frank cerebellar F-18-FDG asymmetry due to symmetrical supratentorial degeneration resulting in a bilateral diaschisis process.

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