When patients first voice concerns about memory, thinking, or daily function impairment, it’s often to their primary care provider. From there, the traditional care pathway toward a potential Alzheimer’s disease (AD) diagnosis has been for the provider to conduct brief cognitive screens and questionnaires. If impairment is identified or suspected, the patient would be sent for amyloid PET scans or cerebrospinal fluid (CSF) testing via lumbar puncture, to a neurology specialist, or both. However, access to these tests as well as specialist appointments can often be limited by availability, wait times, cost, or patient willingness to undergo invasive procedures.
Blood-based Alzheimer’s disease biomarker testing offers a practical, objective tool to help close this gap in the primary care setting. Used as an adjunct to a structured cognitive assessment and standard medical evaluation, these tests can help estimate the likelihood of AD-related pathology from an accessible blood draw—supporting more efficient triage, reducing diagnostic uncertainty when symptoms are ambiguous, and streamlining decisions about referral, additional testing, and early interventions.
In this article:
Clinical challenge | Why it matters | Ordering recommendations | Interpreting test results | Next steps | Supporting resources
Providers witness this gap in their everyday practice
An accessible blood test for Alzheimer’s disease biomarkers can help bridge this diagnostic blind spot by providing objective evidence of AD-related pathology.
Once cognitive impairment is significant enough to be observed through clinical assessment tools, beta-amyloid and phosphorylated tau (p-tau) proteins—both AD biomarkers—may have already been increasing. But blood-based biomarker testing can help identify these microstructural changes in the brain.1
When cognitive screenings suggest impairment but don’t clearly indicate cause, testing for multiple blood-based Alzheimer’s disease biomarkers can more reliably demonstrate quantifiable evidence of amyloid positivity. This helps providers act with greater confidence in 4 clinically meaningful ways.
A positive cognitive screening questionnaire simply indicates the presence of cognitive impairment. Meanwhile, blood-based Alzheimer’s disease biomarkers help assess whether AD pathology is a likely contributor to that impairment. This is an especially useful distinction in mild cognitive impairment (MCI) or early dementia, when functional changes may be subtle and clinical assessment can be unreliable.
For patients with limited or no access to more definitive diagnostic testing, such as PET and CSF, a blood-based biomarker test may be a more affordable—and significantly less invasive—option that bears comparably reliable results.
Blood testing for Alzheimer’s disease biomarkers can help clinicians prioritize who needs and is most likely to benefit from expedited referral, advanced imaging or CSF testing, or evaluation for disease-modifying therapies (DMTs) that require evidence of amyloid pathology.
Earlier definition around a patient’s cognitive status allows for earlier intervention such as counseling and care planning, medication audits to avoid therapies with cognitive side effects, and targeted management of associated risk factors (sleep, depression, hearing, etc).
At the forefront of the latest advances in diagnostics for Alzheimer’s disease, Quest offers the AD-Detect® ABeta 42/40 and p-tau217 Evaluation to test patients showing signs of cognitive impairment. As the key test in the confirmation of amyloid pathology, the panel measures and interprets plasma amyloid ratios (AB42/40) and phosphorylated tau levels (p-tau217) to deliver clinically meaningful insight into patient risk for Alzheimer’s disease development. In patients with cognitive impairment, this panel offers a potential diagnosis, not just assessment of risk.
Blood-based testing for Alzheimer’s disease biomarkers should not replace a traditional clinical evaluation. Instead, it should be used as a complementary tool after a provider has conducted the initial steps in patients ages 55 or older, such as
The AD-Detect® ABeta 42/40 and p-tau217 panel evaluates the symptomatic patient’s plasma AB42/40 ratios and p-tau217 levels. There are 3 possible results that show likelihood of amyloid pathology consistent with AD:
Meeting established parameters for confirmatory testing,8,9 the AD-Detect® ABeta 42/40 and p-tau217 panel evaluates at 91% sensitivity and 91% specificity with a 15% indeterminate rate. These rates are comparable to identifying amyloids with standard-of-care PET scans.
If the AD-Detect® ABeta 42/40 and p-tau217 Evaluation reveals a high likelihood of disease, primary care clinicians can streamline the care pathway. Patients can be referred to the neurology specialty with biomarker results already in hand, making their first specialist visit more efficient. Pre-appointment testing can shorten the path to a definitive Alzheimer’s disease diagnosis and better prepares a patient for a more targeted treatment plan.
In many cases, a high result may eliminate the need for PET or CSF testing. (Note that the choice to do further assessments is with the patient in consultation with their healthcare provider.)
Reach out to receive additional information on Quest’s neurology lab tests, services, and coverage.