Literature DB >> 19819269

N400 to lexical ambiguity and semantic incongruity in schizophrenia.

Dean Salisbury1.   

Abstract

Our previous work showed a semantic bias in interpreting ambiguous words in schizophrenia, with disproportionate misinterpretation of subordinate meanings (toast at a wedding). We proposed pre-selection in schizophrenia of dominant-meaning networks at points of lexical ambiguity, thereby misleading thought. This selection bias may be due to semantic memory hyper-priming causing strong associates to dominate cognition. Alternately, later verbal memory maintenance failure may cause weaker associates to fade more quickly than stronger associates from memory due to less initial activation. To further examine this semantic bias, patients and controls were presented short 4 word long sentences (The toast was buttered). The second word was a homograph or unambiguous noun. The last word disambiguated homographs (dominant or subordinate meaning) or was congruent or incongruent with unambiguous nouns. Previously, we showed increasingly larger N400 from unambiguous associates to dominate associates to subordinate associates to unambiguous non-associates in controls. Pre-selection of dominant meanings predicts that schizophrenia patients would show small N400 to dominant associates and as large N400 to subordinate associates as to incongruous endings. Here, controls again showed graded N400 amplitudes. Patients with schizophrenia showed small N400 to congruent and dominant endings and large N400 to subordinate and incongruous endings. These data suggest early pre-selection of dominant associates in schizophrenia. This effect is unlikely solely due to verbal memory maintenance failure, as patients were able to detect incongruity, albeit with a smaller N400 effect, and displayed generally larger N400 to all stimuli. These results suggest alterations in semantic memory associative networks coupled with verbal working memory maintenance decay in schizophrenia. Copyright 2009 Elsevier B.V. All rights reserved.

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Year:  2009        PMID: 19819269      PMCID: PMC2827669          DOI: 10.1016/j.ijpsycho.2009.10.002

Source DB:  PubMed          Journal:  Int J Psychophysiol        ISSN: 0167-8760            Impact factor:   2.997


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