Official Journal of Japan Society of Ningen Dock
Online ISSN : 2186-5027
Print ISSN : 1880-1021
ISSN-L : 1880-1021
Original Articles
Clinical Potentials of Plasma Aβ40 and Aβ42 Levels and Mild Cognitive Impairment (MCI) Screening (Determining Plasma Apolipoprotein A1, Transthyretin, and Complement C3) as Blood Tests for Detecting Alzheimer’s Disease and MCI, Respectively
Kazuhiko Uchida, Hitomi Ito, Shan Liu, Naoko Hata, Hideaki Suzuki, Kohji Meno, Hiroyasu Akatsu, Hiroyuki Matsukawa, Takashi Asada, Tetsuaki Arai
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2021 Volume 36 Issue 4 Pages 560-567

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Abstract

Objective: Biomarker-based early detection of Alzheimer’s disease (AD) and mild cognitive impairment (MCI) is important for early intervention and prevention of dementia. We previously developed an ‘MCI screening blood test’ involving the testing of triple markers (apolipoprotein A1, transthyretin, and complement protein C3) for the evaluation of cognitive impairment in older adults. In this study, we combined the MCI screening blood test with testing of plasma Aβ40 and Aβ42 levels to evaluate the clinical potential of these five markers in the diagnosis of MCI and AD.

Methods: Through an immunoassay, we measured plasma Aβ40 and Aβ42 levels and triple marker levels in samples of 178 AD, 145 MCI, and 40 cognitively healthy elderly (NDC) patients.

Results: Plasma levels of the triple markers were lower in MCI and AD than in NDC patients. Receiver operating characteristic curve analysis revealed that the composite of triple markers had relative area under the curve (AUC) values of 0.81 and 0.74 in AD vs. NDC and MCI vs. NDC, respectively. The Aβ40/42 ratio had an AUC of 0.71 (AD vs. NDC) and 0.62 (MCI vs. NDC). Furthermore, addition of the triple markers to the Aβ40/42 ratio resulted in AUC values of 0.85 (sensitivity 80%, specificity 85%) in AD vs. NDC and 0.81 (sensitivity 77%, specificity 73%) in MCI vs. NDC.

Conclusion: Blood tests determining these triple markers’ levels and the Aβ40/42 ratio may be useful during routine health checks to evaluate the progression of cognitive impairment in older adults.

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© 2021 Japan Society of Ningen Dock
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