The mismatch negativity as an index of cognitive abilities in adults with Down syndrome

Author:

Saini Fedal12ORCID,Masina Fabio3,Wells Jasmine12,Rosch Richard456,Hamburg Sarah127ORCID,Startin Carla1278,Strydom André127

Affiliation:

1. Department of Forensic and Neurodevelopmental Sciences , Institute of Psychiatry, Psychology & Neuroscience, , 16 De Crespigny Park, London SE5 8AB , UK

2. King’s College London , Institute of Psychiatry, Psychology & Neuroscience, , 16 De Crespigny Park, London SE5 8AB , UK

3. IRCCS San Camillo Hospital , Via Alberoni, 70, 30126 Lido VE , Italy

4. Department of Clinical Neurophysiology, King’s College Hospital NHS Foundation Trust , Golden Jubilee, Denmark Hill, London SE5 9RS , UK

5. Wellcome Centre for Human Neuroimaging , UCL Queen Square Institute of Neurology, , Queen Square, London WC1N 3AR , UK

6. University College London , UCL Queen Square Institute of Neurology, , Queen Square, London WC1N 3AR , UK

7. Division of Psychiatry, University College London , Maple House, 149 Tottenham Ct Rd, London W1T 7BN , UK

8. School of Psychology, University of Roehampton , Grove House, Roehampton Lane, London, SW15 5PJ , UK

Abstract

Abstract Down syndrome (DS) is associated with an ultra-high risk of developing Alzheimer’s disease (AD). Understanding variability in pre-AD cognitive abilities may help understand cognitive decline in this population. The mismatch negativity (MMN) is an event-related potential component reflecting the detection of deviant stimuli that is thought to represent underlying memory processes, with reduced MMN amplitudes being associated with cognitive decline. To further understand the MMN in adults with DS without AD, we explored the relationships between MMN, age, and cognitive abilities (memory, language, and attention) in 27 individuals (aged 17–51) using a passive auditory oddball task. Statistically significant MMN was present only in 18 individuals up to 41 years of age and the latency were longer than canonical parameters reported in the literature. Reduced MMN amplitude was associated with lower memory scores, while longer MMN latencies were associated with poorer memory, verbal abilities, and attention. Therefore, the MMN may represent a valuable index of cognitive abilities in DS. In combination with previous findings, we hypothesize that while MMN response and amplitude may be associated with AD-related memory loss, MMN latency may be associated with speech signal processing. Future studies may explore the potential impact of AD on MMN in people with DS.

Funder

Wellcome Trust Strategic Award

London Down Syndrome Consortium

Baily Thomas Charitable Fund

Medical Research Council

Wellcome Trust

Human Brain Project SGA3

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Cognitive Neuroscience

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