2009
DOI: 10.3174/ajnr.a1545
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Cortical Morphometric Subclassification of Frontotemporal Lobar Degeneration

Abstract: BACKGROUND AND PURPOSE:Frontotemporal lobar degeneration (FTLD) is a primary neurodegenerative disease comprising 3 clinical subtypes: frontotemporal dementia (FTD), semantic dementia (SD), and progressive nonfluent aphasia (PNFA). The subdivision is primarily based on the characteristic clinical symptoms displayed by each subtype. We hypothesized that these symptoms would be correlated to characteristic patterns of brain atrophy, which could be indentified and used for subclassification of subjects with FTLD.

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Cited by 46 publications
(37 citation statements)
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“…Putaminal atrophy on MR imaging may be potentially useful in clinical subtyping of FTLD, in combination with patterns of atrophy in other cortical and subcortical regions. 1,35 These results contrast with our previous study of bilateral caudate volume in FTLD, in which a clear gradient of atrophy, with volumes of controls ϭ AD Ͼ SD Ͼ PNFA Ͼ FTD, was consistent with the expected frontostriatal dysfunction in each subtype of FTLD and for AD and controls. Thus, the putamen seems less clearly implicated as a substrate in frontostriatal circuit dysfunction in FTLD.…”
Section: Discussioncontrasting
confidence: 56%
“…Putaminal atrophy on MR imaging may be potentially useful in clinical subtyping of FTLD, in combination with patterns of atrophy in other cortical and subcortical regions. 1,35 These results contrast with our previous study of bilateral caudate volume in FTLD, in which a clear gradient of atrophy, with volumes of controls ϭ AD Ͼ SD Ͼ PNFA Ͼ FTD, was consistent with the expected frontostriatal dysfunction in each subtype of FTLD and for AD and controls. Thus, the putamen seems less clearly implicated as a substrate in frontostriatal circuit dysfunction in FTLD.…”
Section: Discussioncontrasting
confidence: 56%
“…Pathologically, bvFTD is associated with frontotemporal lobar degeneration [7] and is clinically characterized by progressive changes in personality, social comportment, and cognition [5,8]. Brain imaging techniques, such as positron emission tomography (PET) [9,10], functional MRI [11], structural regions of interest [12,13], and VBM technique [14,15], have long been used to understand the neuroanatomy and neuropathophysiology of this disease. Even brain imaging criteria has been proposed along with the clinical criteria that bvFTD is characterized by bilateral impairment in the frontal and/or temporal brain regions [16,17].…”
Section: Gray Matter Atrophy In Behavioral Variantmentioning
confidence: 99%
“…Participants have been previously described. [19][20][21][22][23] All participants went through the standard investigation procedure at the memory clinic. Clinical diagnoses were determined at a multidisciplinary consensus conference with physicians, neuropsychologists, speech-language pathologists, and nurses.…”
Section: Participantsmentioning
confidence: 99%
“…However, in this study, we were not able to find significant atrophy in the anterior cingulate in FTD. 19 We hypothesized that the anatomic variability of this region caused a larger difference in volume than a potential reduction of volume caused by atrophy.…”
mentioning
confidence: 99%
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