Frontal asymmetry in behavioral variant frontotemporal dementia: clinicoimaging and pathogenetic correlates
- PMID: 22502999
- PMCID: PMC3404265
- DOI: 10.1016/j.neurobiolaging.2012.03.009
Frontal asymmetry in behavioral variant frontotemporal dementia: clinicoimaging and pathogenetic correlates
Abstract
We aimed to assess associations between clinical, imaging, pathologic, and genetic features and frontal lobe asymmetry in behavioral variant frontotemporal dementia (bvFTD). Volumes of the left and right dorsolateral, medial, and orbital frontal lobes were measured in 80 bvFTD subjects and subjects were classified into 3 groups according to the degree of asymmetry (asymmetric left, asymmetric right, symmetric) using cluster analysis. The majority of subjects were symmetric (65%), with 20% asymmetric left and 15% asymmetric right. There were no clinical differences across groups, although there was a trend for greater behavioral dyscontrol in right asymmetric compared with left asymmetric subjects. More widespread atrophy involving the parietal lobe was observed in the symmetric group. Genetic features differed across groups with symmetric frontal lobes associated with C9ORF72 and tau mutations, while asymmetric frontal lobes were associated with progranulin mutations. These findings therefore suggest that neuroanatomical patterns of frontal lobe atrophy in bvFTD are influenced by specific gene mutations.
Copyright © 2013 Elsevier Inc. All rights reserved.
Conflict of interest statement
Figures
References
-
- Ashburner J, Friston KJ. Voxel-based morphometry--the methods. Neuroimage. 2000;11:805–821. - PubMed
-
- Boccardi M, Laakso MP, Bresciani L, Geroldi C, Beltramello A, Frisoni GB. Clinical characteristics of frontotemporal patients with symmetric brain atrophy. Eur Arch Psychiatry Clin Neurosci. 2002;252:235–239. - PubMed
-
- Gass J, Cannon A, Mackenzie IR, Boeve B, Baker M, Adamson J, et al. Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration. Hum Mol Genet. 2006;15:2988–3001. - PubMed
Publication types
MeSH terms
Grants and funding
- R56 AG26251/AG/NIA NIH HHS/United States
- R01-DC010367/DC/NIDCD NIH HHS/United States
- U24 AG021886/AG/NIA NIH HHS/United States
- P50 AG016574/AG/NIA NIH HHS/United States
- R01-NS065782/NS/NINDS NIH HHS/United States
- P50-NS 40256/NS/NINDS NIH HHS/United States
- R01-AG11378/AG/NIA NIH HHS/United States
- R01 AG011378/AG/NIA NIH HHS/United States
- P50-AG25711/AG/NIA NIH HHS/United States
- P50-AG16574/AG/NIA NIH HHS/United States
- R01-AG26251/AG/NIA NIH HHS/United States
- U01-AG06786/AG/NIA NIH HHS/United States
- U01-AG024904/AG/NIA NIH HHS/United States
- R01-AG037491/AG/NIA NIH HHS/United States
- U24-AG026395/AG/NIA NIH HHS/United States
- R21-AG 38736/AG/NIA NIH HHS/United States
- R01 NS065782/NS/NINDS NIH HHS/United States
- R01-NS65782/NS/NINDS NIH HHS/United States
- R01 AG037491/AG/NIA NIH HHS/United States
- P01 AG003949/AG/NIA NIH HHS/United States
- R01-AG15866/AG/NIA NIH HHS/United States
- U01-AG03949/AG/NIA NIH HHS/United States
LinkOut - more resources
Full Text Sources
Other Literature Sources