Corticobasal degeneration: An update.

Ideggyogy Sz

Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, London, UK.

Published: November 2024

AI Article Synopsis

  • Corticobasal degeneration (CBD) is a progressive tauopathy, typically starting between the ages of 50 and 70, marked by neuronal loss and tau protein deposits in various brain regions.
  • CBD is primarily associated with the corticobasal syndrome (CBS), but can also manifest as other clinical conditions, such as frontotemporal dementia and Richardson's syndrome.
  • Definitive diagnosis of CBD requires neuropathological investigation, as specific biomarkers are currently lacking, although recent studies highlight its unique molecular structure compared to other tauopathies.

Article Abstract

Corticobasal degeneration (CBD) is one of the primary tauopathies with a disease onset in the 5th to 7th decade. CBD is a progressive condition of unknown aetiology, which is characterised neuropathologically by neuronal loss, astrogliosis and deposition of filamentous tau inclusions, composed entirely of 4-repeat tau isoforms, in neurons and glial cells in cerebral cortical areas, basal ganglia, brainstem and cerebellar nuclei. The term CBD is now a neuropathological diagnostic one and for the canonical clinical syndrome associated with CBD neuropathological changes, the corticobasal syndrome (CBS) term is used. In addition to CBS, the clinical spectrum also includes a behavioural variant of frontotemporal dementia syndrome, speech disorders, Richardson’s syndrome and, rarely, posterior cortical syndrome. In addition to CBD, CBS can also be caused by other pathologies. A number of genetic risk factors of CBD have been identified. As specific biomarkers confirming CBD as the underlying pathology responsible for CBS or other clinical manifestations are still lacking, for a definitive diagnosis of CBD neuropathological investigation is required. Recent cryo-electron microscopic studies have proven that CBD is a distinct tauopathy associated with a unique molecular structure of the tau filaments, which firmly differentiates it from other primary tauopathies.

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Source
http://dx.doi.org/10.18071/isz.77.0379DOI Listing

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