Pathological correlates of white matter hyperintensities in a case of progranulin mutation associated frontotemporal

Ione O C Woollacott1, Martina Bocchetta1, Carole H Sudre1,2

  • 1a Dementia Research Centre, Department of Neurodegenerative Disease , UCL Institute of Neurology , London , UK.

Neurocase
|August 17, 2018
PubMed

Insights

White matter hyperintensities in progranulin (GRN) mutation frontotemporal dementia are not vascular. Chronic microglial dysfunction may cause selective white matter vulnerability and myelin loss.

Area of Science:

  • Neurology
  • Neuroscience
  • Pathology

Background:

  • White matter hyperintensities (WMH) are common in progranulin (GRN) mutation-associated frontotemporal dementia (FTD).
  • The underlying pathological basis of WMH in this context remains unclear.

Observation:

  • This study investigated WMH pathology in a patient with GRN mutation-associated behavioral variant FTD.
  • In vivo and cadaveric MRI revealed progressive atrophy and asymmetrical WMH, predominantly in frontal regions.
  • Histological analysis focused on regions with varying WMH severity, examining vascular pathology, spongiosis, neuronal/axonal loss, TDP-43, demyelination, astrogliosis, and microglial changes.

Findings:

  • WMH regions showed severe cortical and white matter pathology.
  • Prominent white matter microglial activation and dystrophy were observed.
  • Minimal axonal loss and vascular pathology were noted, suggesting WMH are not primarily vascular-related.

Implications:

  • WMH in GRN mutation carriers are unlikely secondary to vascular issues.
  • Chronic microglial dysfunction due to GRN haploinsufficiency may lead to selective white matter vulnerability and myelin loss.
  • This offers new insights into FTD pathogenesis and potential therapeutic targets.

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