Association of Central Auditory Processing Dysfunction With Preclinical Alzheimer's Disease

Author:

Byun Min Soo12ORCID,Chang Munyoung34ORCID,Yi Dahyun5ORCID,Ahn Hyejin6,Han Dongkyun12,Jeon Seulki7,Jang Hyunsook8,Lee Dong Young125,Oh Seung Ha79,

Affiliation:

1. Department of Psychiatry Seoul National University College of Medicine Seoul South Korea

2. Department of Neuropsychiatry Seoul National University Hospital Seoul South Korea

3. Department of Otolaryngology‐Head and Neck Surgery Chung‐Ang University College of Medicine Seoul South Korea

4. Department of Otolaryngology‐Head and Neck Surgery Chung‐Ang University Hospital Seoul South Korea

5. Institute of Human Behavioral Medicine, Medical Research Centre Seoul National University Seoul South Korea

6. Interdisciplinary Program of Cognitive Science Seoul National University College of Humanities Seoul South Korea

7. Department of Otolaryngology‐Head and Neck Surgery Seoul National University Hospital Seoul South Korea

8. Division of Speech Pathology and Audiology, Research Institute of Audiology & Speech Pathology Hallym University Chuncheon‐si Gangwon‐do South Korea

9. Department of Otolaryngology‐Head and Neck Surgery Seoul National University College of Medicine Seoul South Korea

Abstract

AbstractObjectiveTo investigate whether central auditory processing dysfunction measured by the dichotic digit test‐1 digit (DDT1) is present in preclinical Alzheimer's disease (AD) individuals who are cognitively normal (CN) older adults with the cerebral beta‐amyloid (Aβ) deposition and to explore the potential of the DDT1 as a screening test for preclinical AD.Study DesignCross‐sectional design.SettingA prospective observational cohort study.MethodsCN older adults with a global clinical dementia rating score of 0 were included. The hearing test battery including pure‐tone audiometry, speech audiometry, distortion product otoacoustic emission, and DDT1 was administered to participants.ResultsFifty CN older adults were included. Among them, 38 individuals were included in the Aβ deposition negative (AN) group and 12 were included in the Aβ deposition positive (AP) group. The DDT1 scores of both the better and worse ears were significantly lower in the AP group than in the AN group (p = .008 andp = .015, respectively). No significant differences were observed between the groups in tests of the peripheral auditory pathways. In multivariable logistic regression analysis adjusted for apolipoprotein E4 positivity, the DDT1 better ear score predicted the AP group (p = .036, odds ratio = 0.892, 95% confidence interval: 0.780‐0.985) with relatively high diagnostic accuracy.ConclusionOur findings suggest that Aβ deposition may affect the central auditory pathway even before cognitive decline appears. DDT1, which can easily be applied to the old‐age population, may have the potential as a screening tool for preclinical AD.

Publisher

Wiley

Subject

Otorhinolaryngology,Surgery

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