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Focal temporal pole atrophy and network degeneration in semantic variant primary progressive aphasia.
Collins, Jessica A; Montal, Victor; Hochberg, Daisy; Quimby, Megan; Mandelli, Maria Luisa; Makris, Nikos; Seeley, William W; Gorno-Tempini, Maria Luisa; Dickerson, Bradford C.
Affiliation
  • Collins JA; Department of Neurology, Massachusetts General Hospital/Harvard Medical School, Charlestown, MA, USA jcollins21@mgh.harvard.edu brad.dickerson@mgh.harvard.edu.
  • Montal V; Department of Neurology, Institut d'Investigacions Biomèdiques Sant Pau-Hospital de Sant Pau, Universitat Autònoma de Barcelona, Barcelona, Spain.
  • Hochberg D; Department of Neurology, Massachusetts General Hospital/Harvard Medical School, Charlestown, MA, USA.
  • Quimby M; Department of Neurology, Massachusetts General Hospital/Harvard Medical School, Charlestown, MA, USA.
  • Mandelli ML; Department of Neurology, University of California at San Francisco, San Francisco, CA, USA.
  • Makris N; Department of Psychiatry, Massachusetts General Hospital/Harvard Medical School, Charlestown, MA, USA.
  • Seeley WW; Department of Neurology, University of California at San Francisco, San Francisco, CA, USA.
  • Gorno-Tempini ML; Department of Pathology, University of California at San Francisco, San Francisco, CA, USA.
  • Dickerson BC; Department of Neurology, University of California at San Francisco, San Francisco, CA, USA.
Brain ; 140(2): 457-471, 2017 02.
Article in En | MEDLINE | ID: mdl-28040670
ABSTRACT
A wealth of neuroimaging research has associated semantic variant primary progressive aphasia with distributed cortical atrophy that is most prominent in the left anterior temporal cortex; however, there is little consensus regarding which region within the anterior temporal cortex is most prominently damaged, which may indicate the putative origin of neurodegeneration. In this study, we localized the most prominent and consistent region of atrophy in semantic variant primary progressive aphasia using cortical thickness analysis in two independent patient samples (n = 16 and 28, respectively) relative to age-matched controls (n = 30). Across both samples the point of maximal atrophy was located in the same region of the left temporal pole. This same region was the point of maximal atrophy in 100% of individual patients in both semantic variant primary progressive aphasia samples. Using resting state functional connectivity in healthy young adults (n = 89), we showed that the seed region derived from the semantic variant primary progressive aphasia analysis was strongly connected with a large-scale network that closely resembled the distributed atrophy pattern in semantic variant primary progressive aphasia. In both patient samples, the magnitude of atrophy within a brain region was predicted by that region's strength of functional connectivity to the temporopolar seed region in healthy adults. These findings suggest that cortical atrophy in semantic variant primary progressive aphasia may follow connectional pathways within a large-scale network that converges on the temporal pole.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Semantics / Temporal Lobe / Aphasia, Primary Progressive / Neurodegenerative Diseases Type of study: Clinical_trials / Prognostic_studies Limits: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Brain Year: 2017 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Semantics / Temporal Lobe / Aphasia, Primary Progressive / Neurodegenerative Diseases Type of study: Clinical_trials / Prognostic_studies Limits: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Brain Year: 2017 Document type: Article