4.5 Article

Differential intrinsic functional connectivity changes in semantic variant primary progressive aphasia

期刊

NEUROIMAGE-CLINICAL
卷 22, 期 -, 页码 -

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.nicl.2019.101797

关键词

Primary progressive aphasia; Functional connectivity; Resting-state connectivity; Language; Parietal lobe

资金

  1. National Institutes of Health [NINDS R01NS050915, NIDCD K24DC015544, NIDCD R03DC013403, NIDCD F32DC009145, NIDCD R01DC013270, NIDCD R01DC016291, NIDCD R01DC016345, NIA U01AG052943, NIA P50AG023501, NIA P01AG019724, NIA R01AG038791, NINDS U54NS092089]
  2. Alzheimer's Disease Research Center of California [0375271 DHS/ADP/ARCC]
  3. Larry L. Hillblom Foundation
  4. John Douglas French Alzheimer's Foundation
  5. Koret Family Foundation
  6. Consortium for Frontotemporal Dementia Research
  7. McBean Family Foundation

向作者/读者索取更多资源

The semantic variant of primary progressive aphasia (svPPA) is a clinical syndrome characterized by semantic memory deficits with relatively preserved motor speech, syntax, and phonology. There is consistent evidence linking focal neurodegeneration of the anterior temporal lobes (ATL) to the semantic deficits observed in svPPA. Less is known about large-scale functional connectivity changes in this syndrome, particularly regarding the interplay between affected and spared language networks that leads to the unique cognitive dissociations typical of svPPA. Using whole-brain, seed-based connectivity on task-free Magnetic Resonance Imaging (MRI) data, we studied connectivity of networks anchored to three left-hemisphere regions crucially involved in svPPA symptomatology: ATL just posterior to the main atrophic area, opercular inferior frontal gyrus, and posterior inferior temporal lobe. First, in 32 healthy controls, these seeds isolated three networks: a ventral semantic network involving anterior middle temporal and angular gyri, a dorsal articulatory-phonological system involving inferior frontal and supramarginal regions, and a third functional connection between posterior inferior temporal and intraparietal regions likely involved in linking visual and linguistic processes. We then compared connectivity strength of these three networks between 16 svPPA patients and the 32 controls. In svPPA, decreased functional connectivity in the ventral semantic network correlated with weak semantic skills, while connectivity of the network seeded from the posterior inferior temporal lobe, though not significantly different between the two groups, correlated with pseudoword reading skills. Increased connectivity between the inferior frontal gyrus and the superior portion of the angular gyrus suggested possible adaptive changes. Our findings have two main implications. First, they support a functional subdivision of the left IPL based on its connectivity to specific language-related regions. Second, the unique neuroanatomical and linguistic profile observed in svPPA provides a compelling model for the functional interplay of these networks, being either up- or down- regulated in response to disease.

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