Association Between Plasma Amyloid-β and Neuropsychological Performance in Patients With Cognitive Decline
Objective: To investigate the association between plasma amyloid-β (Aβ) levels and neuropsychological performance in patients with cognitive decline using a highly sensitive nano-biosensing platform. Methods: We prospectively recruited 44 patients with cognitive decline who underwent plasma Aβ analy...
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Veröffentlicht in: | Frontiers in aging neuroscience 2021-10, Vol.13, p.736937-736937 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Objective:
To investigate the association between plasma amyloid-β (Aβ) levels and neuropsychological performance in patients with cognitive decline using a highly sensitive nano-biosensing platform.
Methods:
We prospectively recruited 44 patients with cognitive decline who underwent plasma Aβ analysis, amyloid positron emission tomography (PET) scanning, and detailed neuropsychological tests. Patients were classified into a normal control (NC,
n
= 25) or Alzheimer’s disease (AD,
n
= 19) group based on amyloid PET positivity. Multiple linear regression was performed to determine whether plasma Aβ (Aβ
40
, Aβ
42
, and Aβ
42/40
) levels were associated with neuropsychological test results.
Results:
The plasma levels of Aβ
42/40
were significantly different between the NC and AD groups and were the best predictor of amyloid PET positivity by receiver operating characteristic curve analysis [area under the curve of 0.952 (95% confidence interval, 0.892–1.000)]. Although there were significant differences in the neuropsychological performance of cognitive domains (language, visuospatial, verbal/visual memory, and frontal/executive functions) between the NC and AD groups, higher levels of plasma Aβ
42/40
were negatively correlated only with verbal and visual memory performance.
Conclusion:
Our results demonstrated that plasma Aβ analysis using a nano-biosensing platform could be a useful tool for diagnosing AD and assessing memory performance in patients with cognitive decline. |
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ISSN: | 1663-4365 1663-4365 |
DOI: | 10.3389/fnagi.2021.736937 |