Structural correlates of language processing in primary progressive aphasia

被引:4
作者
Chapman, Curtiss A. [1 ,17 ]
Polyakova, Maryna [2 ,3 ]
Mueller, Karsten [2 ]
Weise, Christopher [3 ,4 ]
Fassbender, Klaus [5 ]
Fliessbach, Klaus [6 ,7 ]
Kornhuber, Johannes [8 ]
Lauer, Martin [9 ]
Anderl-Straub, Sarah [10 ]
Ludolph, Albert [10 ]
Prudlo, Johannes [7 ,11 ]
Staiger, Anja [12 ]
Synofzik, Matthis [7 ,13 ]
Wiltfang, Jens [7 ,14 ]
Riedl, Lina [15 ]
Diehl-Schmid, Janine [15 ]
Otto, Markus [10 ]
Danek, Adrian [16 ]
Hartwigsen, Gesa [1 ]
Schroeter, Matthias L. [2 ,3 ]
机构
[1] Max Planck Inst Human Cognit & Brain Sci, Lise Meitner Grp Cognit & Plast, D-04103 Leipzig, Germany
[2] Max Planck Inst Human Cognit & Brain Sci, Dept Neurol, D-04103 Leipzig, Germany
[3] Univ Leipzig, Med Ctr, Dept Neurol, D-04103 Leipzig, Germany
[4] Univ Halle, Med Ctr, Dept Neurol, D-06120 Halle, Germany
[5] Saarland Univ Hosp, Dept Neurol, D-66421 Homburg, Germany
[6] Univ Hosp Bonn, Dept Psychiat & Psychotherapy, D-53127 Bonn, Germany
[7] German Ctr Neurodegenerat Dis DZNE, Gottingen, Germany
[8] Univ Hosp Erlangen, Dept Psychiat & Psychotherapy, D-91054 Erlangen, Germany
[9] Univ Hosp Wurzburg, Dept Psychiat & Psychotherapy, D-97080 Wurzburg, Germany
[10] Univ Ulm, Dept Neurol, D-89081 Ulm, Germany
[11] Univ Med Rostock, Dept Neurol, D-18051 Rostock, Germany
[12] Ludwig Maximilians Univ Munchen, Inst Phonet & Speech Proc, Clin Neuropsychol Res Grp, D-80539 Munich, Germany
[13] Hertie Inst Clin Brain Res, Ctr Neurol, Dept Neurodegenerat Dis, D-72076 Tubingen, Germany
[14] Med Univ Gottingen, Dept Psychiat & Psychotherapy, D-37075 Gottingen, Germany
[15] Tech Univ Munich, Dept Psychiat & Psychotherapy, D-80333 Munich, Germany
[16] Ludwig Maximilians Univ Munchen, Dept Neurol, D-80539 Munich, Germany
[17] Max Planck Inst Human Cognit & Brain Sci, Lise Meitner Res Grp Cognit & Plast, Stephanstr 1a, D-04103 Leipzig, Germany
关键词
primary progressive aphasia; language; semantics; cortical thickness; TEMPORAL INVOLVEMENT; LOGOPENIC VARIANT; VERBAL FLUENCY; ATROPHY; PERFORMANCE; PATTERNS; ANATOMY; BASES;
D O I
10.1093/braincomms/fcad076
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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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页数:10
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