Abstract

BackgroundAlzheimer’s disease (AD) is an irreversible neurodegenerative disease characterized by the hallmark finding of cerebral amyloid deposition. Many researchers have tried to predict the existence of cerebral amyloid deposition by using easily accessible blood plasma samples, but the effectiveness of such strategies remains controversial.MethodsWe developed a new multiplex kit, the QPLEX™ Alz plus assay kit, which uses proteomics-based blood biomarkers to prescreen for cerebral amyloid deposition. A total of 300 participants who underwent Pittsburgh compound B (PiB)-positron emission tomography (PET) which allows imaging of cerebral amyloid deposition were included in this study. We compared the levels of QPLEX™ biomarkers between patients who were classified as PiB-negative or PiB-positive, regardless of their cognitive function. Logistic regression analysis followed by receiver operating characteristic (ROC) curve analysis was performed. The kit accuracy was tested using a randomized sample selection method.ResultsThe results obtained using our assay kit reached 89.1% area under curve (AUC) with 80.0% sensitivity and 83.0% specificity. Further validation of the QPLEX™ Alz plus assay kit using a randomized sample selection method showed an average accuracy of 81.5%.ConclusionsOur QPLEX™ Alz plus assay kit provides preliminary evidence that it can be used as blood marker to predict cerebral amyloid deposition but independent validation is needed.

Highlights

  • Alzheimer’s disease (AD) is an irreversible neurodegenerative disease characterized by the hallmark finding of cerebral amyloid deposition

  • We revealed a novel blood-based biomarker panel for cerebral amyloid deposition consisting of galectin-3 binding protein (LGALS3BP), Aβ1–40, angiotensin-converting enzyme (ACE), and periostin (POSTN) [3, 4]

  • We developed a new AD diagnostic kit, the QPLEXTM Alz plus assay kit, which predicts cerebral amyloid deposition using our previously developed blood biomarkers, LGALS3BP, Aβ1–40, ACE, and POSTN

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Summary

Introduction

Alzheimer’s disease (AD) is an irreversible neurodegenerative disease characterized by the hallmark finding of cerebral amyloid deposition. Many researchers have tried to predict the existence of cerebral amyloid deposition by using accessible blood plasma samples, but the effectiveness of such strategies remains controversial. In the early stages of the disease, when pathological hallmarks exist in the brain but no clinical symptom is seen, patients would be unlikely to undergo a brain PET scan [2, 3]. This a major obstacle when early diagnosis relies on PET. Many researchers and clinicians have noted that the use of efficient, early, and accessible diagnostic methods could prevent or delay the progress of AD pathology

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