4.0 Article

Structural correlates of language processing in primary progressive aphasia

Journal

BRAIN COMMUNICATIONS
Volume 5, Issue 2, Pages -

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/braincomms/fcad076

Keywords

primary progressive aphasia; language; semantics; cortical thickness

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Understanding the relationship between brain structure and language behavior in primary progressive aphasia is crucial for understanding the pathomechanisms of these diseases. This study found that there are networks of language task-associated brain regions, some of which show atrophy and others do not, suggesting regions of future network disruption and providing insights into task deficits beyond atrophied cortex.
Understanding the relationships between brain structure and language behaviour in primary progressive aphasia provides crucial information about these diseases' pathomechanisms. However, previous investigations have been limited from providing a statistically reliable view of broad language abilities by sample size, variant focus and task focus. In this study, the authors aimed to determine the relationship between brain structure and language behaviour in primary progressive aphasia, to determine the degree to which task-associated regions were atrophied across disease variants and to determine the degree to which task-related atrophy overlaps across disease variants. Participants were 118 primary progressive aphasia patients and 61 healthy, age-matched controls tested from 2011 to 2018 in the German Consortium for Frontotemporal Lobar Degeneration cohort. Diagnosis of primary progressive aphasia required progressive deterioration of mainly speech and language for >= 2 years, and variant was diagnosed by the criteria of Gorno-Tempini et al. (Classification of primary progressive aphasia and its variants. Neurology. 2011;76(11):1006-1014). Twenty-one participants not fulfilling a specific subtype were classified as mixed-variant and excluded. Language tasks of interest included the Boston naming test, a German adaptation of the Repeat and Point task, phonemic and category fluency tasks and the reading/writing subtest of the Aachen Aphasia Test. Brain structure was measured by cortical thickness. We observed networks of language task-associated temporal, frontal and parietal cortex. Overlapping task-associated atrophy was observed in the left lateral, ventral and medial temporal lobes, middle and superior frontal gyri, supramarginal gyrus and insula. Some regions, primarily in the perisylvian region, were associated with language behaviour despite showing no significant atrophy. The results crucially extend less powerful studies associating brain and language measures in primary progressive aphasia. Cross-variant atrophy in task-associated regions suggests partially shared underlying deficits, whereas unique atrophy reinforces variant-specific deficits. Language task-related regions that are not obviously atrophied suggest regions of future network disruption and encourage understanding of task deficits beyond clearly atrophied cortex. These results may pave the way for new treatment approaches. In 118 patients with primary progressive aphasia, Chapman et al. found that language tasks associated with cortical thickness in temporal, frontal and parietal brain regions. Cross-variant atrophy suggested shared underlying deficits; unique atrophy reinforced variant-specific deficits; and unatrophied, language-related regions suggested regions of future network disruption.

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