Are frontal cognitive and atrophy patterns different in PSP and bvFTD? A comparative neuropsychological and VBM study

PLoS One. 2013 Nov 20;8(11):e80353. doi: 10.1371/journal.pone.0080353. eCollection 2013.

Abstract

Progressive supranuclear palsy (PSP) and frontotemporal lobar degeneration (FTD) are two clinicohistological entities that share a severe prefrontal syndrome. To what extent do the cognitive syndrome and the location of the underlying brain atrophy unify or segregate these entities? Here, we examined the clinical and radiological patterns of frontal involvement and the neural bases of the cognitive dysfunctions observed in the Richardson form of PSP and the behavioral variant of FTD (bvFTD). The cognitive profile and grey and white matter volume of PSP (n = 19) and bvFTD (n = 16) patients and control participants (n = 18) were compared using a standard battery of neuropsychological tests and voxel-based morphometry (VBM), respectively. Analyses of correlations between neuropsychological and morphometric data were additionally performed. The severity and qualitative pattern of cognitive dysfunction was globally similar between the two patient groups. Grey matter volume was decreased in widespread frontal areas and in the temporal uncus in bvFTD, while it was decreased in the frontal and temporal lobes as well as in the thalamus in PSP. We also found an unexpected involvement of the frontal rectal gyrus in PSP patients compared to controls. Correlation analyses yielded different results in the two groups, with no area showing significant correlations in PSP patients, while several frontal and some temporal areas did so in bvFTD patients. In spite of minor neuropsychological and morphological differences, this study shows that the patterns of cognitive dysfunction and atrophy are very similar in PSP and bvFTD. However, executive dysfunction in these diseases may stem from partially divergent cortical and subcortical neural circuits.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Case-Control Studies
  • Cognition*
  • Female
  • Frontal Lobe / pathology*
  • Frontal Lobe / physiopathology
  • Frontotemporal Lobar Degeneration / pathology*
  • Frontotemporal Lobar Degeneration / physiopathology
  • Humans
  • Male
  • Middle Aged
  • Neuropsychological Tests*
  • Prospective Studies
  • Supranuclear Palsy, Progressive / pathology*
  • Supranuclear Palsy, Progressive / physiopathology

Grants and funding

This work was supported by the JNLF (for Julien Lagarde), and the INSERM. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.