This includes our panel, AD-Detect™ ABeta 42/40 and p-tau217 Evaluation, which combines Aβ 42/40 and p-tau217 plasma levels to help establish the likelihood of amyloid pathology consistent with Alzheimer's disease, evaluated at 91% sensitivity and 91% specificity—meeting accepted performance standards for blood-based biomarker tests.9,10
The biomarker values are combined into a single analytical interpretation, which has been shown to significantly improve predictive performance and accuracy for detecting amyloid positivity corresponding to the findings of an amyloid PET scan and establishing a diagnosis of Alzheimer's disease.