White matter tauopathy with globular glial inclusions: A distinct sporadic frontotemporal lobar segeneration

Gabor G. Kovacs, Katalin Majtenyi, Salvatore Spina, Jill R. Murrell, Ellen Gelpi, Romana Hoftberger, Graham Fraser, R. Anthony Crowther, Michel Goedert, Herbert Budka, Bernardino Ghetti

Research output: Contribution to journalArticle

87 Citations (Scopus)

Abstract

Frontotemporal lobar degenerations are a group of disorders characterized by circumscribed degeneration of the frontal and temporal lobes and diverse histopathologic features. We report clinical, neuropathologic, ultrastructural, biochemical, and genetic data on 7 individuals with a 4-repeat tauopathy characterized by the presence of globular glial inclusions (GGIs) in brain white matter. Clinical manifestations were compatible with the behavioral variant of frontotemporal dementia and included motor neuron symptoms; there was prominent neuronal loss in the frontal and temporal cortex, subiculum, and amygdala. The surrounding white matter showed abundant GGIs composed of abnormal filaments present mostly in oligodendrocytes. The severity of white matter tau abnormalities correlated with a reduction in myelin and axons and with microglial activation. Western blotting of sarkosyl-insoluble tau demonstrated the presence of 2 major tau bands of 64 and 68 kd. No mutations in the microtubule-associated protein tau gene were detected in 2 affected individuals. We propose that 4-repeat tau-immunoreactive GGIs are the neuropathologic hallmark of a distinct sporadic tauopathy with variable clinical presentations that include frontotemporal dementia and occasionally upper motor neuron disease. This type of tauopathy with GGIs expands the group of neurodegenerativedisorders in which oligodendroglial pathology predominates, beyond the synucleinopathy multiple system atrophy disorders.

Original languageEnglish
Pages (from-to)963-975
Number of pages13
JournalJournal of Neuropathology and Experimental Neurology
Volume67
Issue number10
DOIs
StatePublished - Oct 2008

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Tauopathies
Neuroglia
Frontotemporal Dementia
Frontal Lobe
Temporal Lobe
Frontotemporal Lobar Degeneration
Multiple System Atrophy
Motor Neuron Disease
Microtubule-Associated Proteins
Oligodendroglia
Motor Neurons
Myelin Sheath
Amygdala
Axons
Molecular Biology
Hippocampus
Western Blotting
Pathology
Mutation
White Matter

Keywords

  • Dementia
  • Frontotemporal lobar degeneration
  • Tau
  • Tauopathy
  • White matter

ASJC Scopus subject areas

  • Pathology and Forensic Medicine
  • Clinical Neurology
  • Neurology
  • Cellular and Molecular Neuroscience

Cite this

White matter tauopathy with globular glial inclusions : A distinct sporadic frontotemporal lobar segeneration. / Kovacs, Gabor G.; Majtenyi, Katalin; Spina, Salvatore; Murrell, Jill R.; Gelpi, Ellen; Hoftberger, Romana; Fraser, Graham; Crowther, R. Anthony; Goedert, Michel; Budka, Herbert; Ghetti, Bernardino.

In: Journal of Neuropathology and Experimental Neurology, Vol. 67, No. 10, 10.2008, p. 963-975.

Research output: Contribution to journalArticle

Kovacs, GG, Majtenyi, K, Spina, S, Murrell, JR, Gelpi, E, Hoftberger, R, Fraser, G, Crowther, RA, Goedert, M, Budka, H & Ghetti, B 2008, 'White matter tauopathy with globular glial inclusions: A distinct sporadic frontotemporal lobar segeneration', Journal of Neuropathology and Experimental Neurology, vol. 67, no. 10, pp. 963-975. https://doi.org/10.1097/NEN.0b013e318187a80f
Kovacs, Gabor G. ; Majtenyi, Katalin ; Spina, Salvatore ; Murrell, Jill R. ; Gelpi, Ellen ; Hoftberger, Romana ; Fraser, Graham ; Crowther, R. Anthony ; Goedert, Michel ; Budka, Herbert ; Ghetti, Bernardino. / White matter tauopathy with globular glial inclusions : A distinct sporadic frontotemporal lobar segeneration. In: Journal of Neuropathology and Experimental Neurology. 2008 ; Vol. 67, No. 10. pp. 963-975.
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