Proteasome Activity in the Plasma as a Novel Biomarker in Mild Cognitive Impairment with Chronic Tinnitus

Authors
Yun, YejinLee, Sang-YeonChoi, Won HoonPark, Jong-ChanLee, Dong HanKim, Yun KyungLee, Jung HoonLee, Jun-YoungLee, Min JaeKim, Young Ho
Issue Date
2020-10
Publisher
IOS PRESS
Citation
JOURNAL OF ALZHEIMERS DISEASE, v.78, no.1, pp.195 - 205
Abstract
Background: Although the existence of proteasomes in human blood, termed circulating proteasomes (c-proteasomes), has been reported previously, their origin and pathophysiological functions remain largely unknown. Objective: Given that c-proteasome activity was significantly reduced in Alzheimer's disease model mice and relatively high frequency of mild cognitive impairment (MCI) is accompanied by chronic tinnitus in aged patients, we examined whether c-proteasome activity in human plasma was associated with cognitive function in patients with chronic tinnitus. Methods: c-Proteasome activity in the plasma of tinnitus patients (N = 55) was measured with fluorogenic reporter substrate, suc-LLVY-AMC. To assess MCI, the Montreal Cognitive Assessmentwas conducted with a cut-off score of 22/23. All patients underwent audiological and psychoacoustic analyses. Levels of c-proteasomes, A beta(42), and A beta(40) were measured using ELISA, and their association with c-proteasome activity was evaluated. Results: The activity of circulating proteasomes was significantly lower in patients with chronic tinnitus and MCI (p = 0.042), whereas activities of other plasma enzymes showed little correlation. In addition, c-proteasome activity was negatively associated with the level of plasma A beta and was directly dependent on its own concentration in the plasma of patients with chronic tinnitus. Conclusion: Our current work provides a new perspective for understanding the potential relationship between circulating proteasomes in the plasma and cognitive dysfunction, suggesting a novel, non-invasive biomarker in the context of MCI diagnosis.
Keywords
CIRCULATING PROTEASOMES; HEARING-LOSS; WORKING-MEMORY; 20S PROTEASOME; MOUSE MODEL; ALZHEIMERS; RISK; BETA; TAU; CIRCULATING PROTEASOMES; HEARING-LOSS; WORKING-MEMORY; 20S PROTEASOME; MOUSE MODEL; ALZHEIMERS; RISK; BETA; TAU; Amyloid-beta; biomarker; mild cognitive impairment; plasma; proteasome; tinnitus
ISSN
1387-2877
URI
https://pubs.kist.re.kr/handle/201004/118026
DOI
10.3233/JAD-200728
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KIST Article > 2020
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