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Auditory cortical activity in amnestic mild cognitive impairment: relationship to subtype and conversion to dementia
Edward J Golob1, Rie Irimajiri, Arnold Starr
1Department of Neurology, University of California, Irvine, CA, USA. egolob@tulane.edu
Abstract:
Mild cognitive impairment (MCI) patients have a high risk of converting to Alzheimer's disease. The most common diagnostic subtypes of MCI have an episodic memory disorder (amnestic MCI) occurring either alone [single domain (SD)] or with other cognitive impairments [multiple domain (MD)]. Previous studies report increased amplitudes of auditory cortical potentials in MCI, but their relationships to MCI subtypes and clinical outcomes were not defined. We studied subjects with amnestic MCI (n = 41: 28 SD, 13 MD), Alzheimer's disease (n = 14), and both younger (n = 22) and age-matched older controls (n = 44). Baseline auditory sensory (P50, N100) and cognitive potentials (P300) were recorded during an auditory discrimination task. MCI patients were followed for up to 5 years, and outcomes were classified as (i) continued diagnosis of MCI (MCI-stable, n = 16), (ii) probable Alzheimer's disease (MCI-convert, n = 18), or other outcomes (n = 7). Auditory potentials were analysed as a function of MCI diagnosis and outcomes, and compared with young, older controls, and mild Alzheimer's disease subjects. P50 amplitude increased with normal ageing, and had additional increases in MCI as a function of both initial diagnosis (MD > than SD) and outcome (MCI-convert > MCI-stable). P300 latency increased with normal ageing, and had additional increases in MCI but did not differ among outcomes. We conclude that auditory cortical sensory potentials differ among amnestic MCI subtypes and outcomes occurring up to 5 years later.
Insights
Auditory sensory potentials, specifically P50 amplitude, show distinct patterns in mild cognitive impairment (MCI) patients. These changes can differentiate subtypes and predict conversion to Alzheimer's disease, offering a potential diagnostic biomarker.
Area of Science:
- Neuroscience
- Clinical Neurology
- Biomarkers
Background:
- Mild cognitive impairment (MCI) is a precursor to Alzheimer's disease (AD).
- Amnestic MCI, characterized by episodic memory deficits, has subtypes: single domain (SD) and multiple domain (MD).
- Previous research noted altered auditory cortical potentials in MCI, but subtype and outcome associations were unclear.
Purpose of the Study:
- To investigate auditory sensory and cognitive potentials (P50, N100, P300) in amnestic MCI subtypes.
- To determine the relationship between these potentials and clinical outcomes (MCI-stable vs. MCI-convert to AD) over 5 years.
- To compare findings in MCI with young controls, older controls, and mild AD patients.
Main Methods:
- Auditory evoked potentials (P50, N100, P300) were recorded during an auditory discrimination task.
- Participants included amnestic MCI (SD and MD subtypes), probable AD, young controls, and age-matched older controls.
- MCI patients were followed for up to 5 years to classify outcomes: MCI-stable or MCI-convert to probable AD.
Main Results:
- P50 amplitude increased with normal aging and was further elevated in MCI.
- Elevated P50 amplitude was significantly higher in multiple domain (MD) MCI than single domain (SD) MCI.
- Higher P50 amplitude in MCI predicted conversion to probable AD (MCI-convert > MCI-stable).
- P300 latency increased with aging and MCI, but did not differentiate outcomes.
Conclusions:
- Auditory sensory potentials, particularly P50 amplitude, differ between amnestic MCI subtypes.
- P50 amplitude serves as a potential biomarker for predicting progression from MCI to Alzheimer's disease.
- These findings highlight the utility of auditory evoked potentials in understanding MCI heterogeneity and prognosis.
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