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  Lesion correlates of patholinguistic profiles in chronic aphasia: Comparisons of syndrome-, modality- and symptom-level assessment

Obrig, H., Henseler, I., & Regenbrecht, F. (2014). Lesion correlates of patholinguistic profiles in chronic aphasia: Comparisons of syndrome-, modality- and symptom-level assessment. Brain, 137(3), 918-930. doi:10.1093/brain/awt374.

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Item Permalink: http://hdl.handle.net/11858/00-001M-0000-0014-B4F5-2 Version Permalink: http://hdl.handle.net/21.11116/0000-0003-81C5-C
Genre: Journal Article

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 Creators:
Obrig, Hellmuth1, Author              
Henseler, Ilona1, Author              
Regenbrecht, F.2, Author
Affiliations:
1Department Neurology, MPI for Human Cognitive and Brain Sciences, Max Planck Society, ou_634549              
2External Organizations, ou_persistent22              

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Free keywords: lesion-deficit analysis; VLSM; chronic aphasia; aphasia syndromes; linguistic modalities
 Abstract: One way to investigate the neuronal underpinnings of language competence is to correlate patholinguistic profiles of aphasic patients to corresponding lesion sites. Constituting the beginnings of aphasiology and neurolinguistics over a century ago, this approach has been revived and refined in the past decade by statistical approaches mapping continuous variables (providing metrics that are not simply categorical) on voxel-wise lesion information (voxel-based lesion–symptom mapping). Here we investigate whether and how voxel-based lesion–symptom mapping allows us to delineate specific lesion patterns for differ- entially fine-grained clinical classifications. The latter encompass ‘classical’ syndrome-based approaches (e.g. Broca’s aphasia), more symptom-oriented descriptions (e.g. agrammatism) and further refinement to linguistic sub-functions (e.g. lexico-semantic deficits for inanimate versus animate items). From a large database of patients treated for aphasia of different aetiologies ( n= 1167) a carefully selected group of 102 first ever ischaemic stroke patients with chronic aphasia ( ; 12 months) were included in a VLSM analysis. Specifically, we investigated how performance in the Aachen Aphasia Test—the standard clinical test battery for chronic aphasia in German—relates to distinct brain lesions. The Aachen Aphasia Test evaluates aphasia on different levels: a non-parametric discriminant procedure yields probabilities for the allocation to one of the four ‘standard’ syndromes (Broca, Wernicke, global and amnestic aphasia), whereas standardized subtests target linguistic modalities (e.g. repe- tition), or even more specific symptoms (e.g. phoneme repetition). Because some subtests of the Aachen Aphasia Test (e.g. for the linguistic level of lexico-semantics) rely on rather coarse and heterogeneous test items we complemented the analysis with a number of more detailed clinically used tests in selected mostly mildly affected subgroups of patients. Our results indicate that: (i) Aachen Aphasia Test-based syndrome allocation allows for an unexpectedly concise differentiation between ‘Broca’s’ and ‘Wernicke’s’ aphasia corresponding to non-overlapping anterior and posterior lesion sites; whereas (ii) analyses for modalities and specific symptoms yielded more circumscribed but partially overlapping lesion foci, often cutting across the above syndrome territories; and (iii) especially for lexico-semantic capacities more specialized clinical test-batteries are required to delineate precise lesion patterns at this linguistic level. In sum this is the first report on a successful lesion-delineation of syndrome-based aphasia classification highlighting the relevance of vascular distribution for the syndrome level while confirming and extending a number of more linguistically motivated differentiations, based on clinically used tests. We consider such a comprehensive view reaching from the syndrome to a fine-grained symptom-oriented assessment mandatory to converge neurolinguistic, patholin- guistic and clinical-therapeutic knowledge on language-competence and impairment.

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Language(s): eng - English
 Dates: 2013-11-252014-02-132014-03
 Publication Status: Published in print
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Method: Peer
 Identifiers: DOI: 10.1093/brain/awt374
PMID: 24525451
Other: Epub 2014
 Degree: -

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Title: Brain
  Other : Brain
Source Genre: Journal
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Publ. Info: London : Macmillan
Pages: - Volume / Issue: 137 (3) Sequence Number: - Start / End Page: 918 - 930 Identifier: ISSN: 0006-8950
CoNE: /journals/resource/954925385135