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Article type: Research Article
Authors: Mowszowski, Lorena; b | Hermens, Daniel F.c | Diamond, Keria | Norrie, Louisaa | Hickie, Ian B.c | Lewis, Simon J.G.a | Naismith, Sharon L.a; *
Affiliations: [a] Ageing Brain Centre, Brain and Mind Research Institute, The University of Sydney, NSW, Australia | [b] Department of Psychology, Macquarie University, NSW, Australia | [c] Clinical Research Unit, Brain and Mind Research Institute, The University of Sydney, NSW, Australia
Correspondence: [*] Correspondence to: A/Prof Sharon Naismith, Ageing Brain Centre, Brain & Mind Research Institute, The University of Sydney, Level 4, 94 Mallett St, Camperdown NSW, 2050, Australia. Tel.: +612 9351 0781, Fax: +612 9351 0855, E-mail: sharon.naismith@sydney.edu.au.
Abstract: Mild cognitive impairment (MCI) refers to a transitory state between healthy aging and dementia. Biomarkers are needed to facilitate early identification of MCI and predict progression to dementia. One potential neurophysiological biomarker, mismatch negativity (MMN), is an event-related potential reflecting fundamental, pre-attentive cognitive processes. MMN is reduced in normal aging and dementia and in neuropsychiatric samples and is associated with verbal memory deficits and poor executive functioning. This study aimed to investigate auditory MMN and its relationship to neuropsychological performance in MCI. Twenty-eight MCI participants and fourteen controls, aged ≥50 years, underwent neurophysiological and neuropsychological assessment, and completed questionnaires pertaining to disability. Relative to controls, the MCI group demonstrated reduced temporal MMN amplitude (p < 0.01). Reduced right temporal MMN was significantly associated with poorer verbal learning (r = 0.496; p < 0.01) and reduced left temporal MMN was significantly associated with increased self-reported disability (r = −0.419; p < 0.05). These results indicate that patients with MCI exhibit altered pre-attentive information processing, which in turn is associated with memory and psychosocial deficits. These findings overall suggest that MMN may be a viable neurophysiological biomarker of underlying disease in this ‘at risk’ group.
Keywords: Event-related potential, memory, mild cognitive impairment, mismatch negativity, neuropsychological
DOI: 10.3233/JAD-2012-111868
Journal: Journal of Alzheimer's Disease, vol. 30, no. 1, pp. 209-219, 2012
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