Alzheimer’s Disease Assessment Panel

Integrating Tau–Amyloid and APOE for Precision Cognitive Insight

Overview​

The Alzheimer’s Disease Assessment Panel equips clinicians with a clear, integrated view of both current brain pathology and long-term genetic susceptibility to Alzheimer’s disease. By combining an FDA-cleared blood-based biomarker test with APOE genotyping, this panel enables earlier risk awareness, more informed clinical decisions, and personalized brain-health strategies.

Unlike traditional assessments that rely solely on symptoms or family history, this panel delivers objective biological insight helping clinicians identify Alzheimer’s-related changes before cognitive symptoms become clinically obvious.

Alzheimer’s Disease Assessment Panel with ApoE​

What This Test Covers

FDA-Cleared Lumipulse® pTau217 /
Aβ1-42 Plasma Ratio Test

This panel includes the FDA-cleared Lumipulse® blood test, offering a less invasive and more accessible alternative to PET imaging or cerebrospinal fluid analysis.

It evaluates two critical Alzheimer’s-associated biomarkers:

  • pTau217
  • β-Amyloid 1-42 (Aβ1-42)

The pTau217 / Aβ1-42 ratio provides insight into early amyloid-related brain changes, often preceding noticeable memory loss or cognitive decline. This allows clinicians professionals to identify biological risk earlier in the disease continuum.

Health Support Insights

  • Cognitive Exercise Training Evidence-informed activities that support neuroplasticity, memory, and long-term brain resilience aligned with the individual’s overall risk profile.

  • Nutritional Insights Targeted nutrition insights to support amyloid clearance, mitochondrial health, and inflammation balance.

  • Lifestyle Strategies Key modifiable factors including sleep, stress, metabolic health, and cardiovascular function.

  • Supplement Insights Evidence-based supplement insights aligned with individual biological and genetic context.

  • Labs to Consider Select laboratory markers to support clinical decision-making and further personalize nutrition, lifestyle, and supplement strategies.

APOE Genotype Analysis

The report includes APOE genotyping, the most extensively studied genetic factor in late-onset Alzheimer’s disease.
● APOE-ε4
● APOE-ε2
● APOE-ε3
This genetic layer provides context for lifetime susceptibility, helping clinicians tailor risk communication and preventive strategies.

Integrated Risk Interpretation -
Biological Activity + Genetic Predisposition

By uniting current biomarker activity with genetic risk, this panel delivers a more complete and clinically meaningful Alzheimer’s risk profile. Clinicians gain clarity on whether changes reflect active pathology, inherited vulnerability, or both, enabling smarter monitoring and earlier action.

Why It Matters

Alzheimer’s disease begins years, often decades before diagnosis. Relying on symptoms alone delays intervention.
This panel allows clinicians to

By integrating biomarkers and genetics, providers can shift the focus from late diagnosis to early action.

Who Should Take This Test

This panel is designed for

Physicians and neurologists

Physicians and neurologists

Preventive and longevity-focused clinicians

Functional and integrative medicine practitioners

Clinicians managing patients with memory concerns or family history of dementia

Ideal for practices aiming to deliver proactive, precision-driven cognitive health care

What You’ll Receive

ExtendingME Lab Analysis

Comprehensive Report

• FDA-cleared pTau217 / Aβ1-42 blood biomarker results
• APOE genotype analysis with clear interpretation
Integrated Alzheimer’s risk overview

Your Journey Begins

Personalized Insights

Clinically relevant insights across cognition, nutrition, lifestyle, supplements and labs to consider.

Continued Education

Provider Portal Access

Secure digital access to the ExtendingME Provider Portal for test ordering and result tracking.

Congenital Disease Risk Management

Turnaround Time

Results will be available approximately 2 weeks from the receipt of the sample and will be securely delivered through the Provider Portal, allowing efficient review and patient follow-up.

Collection Method

ExtendingME kits include all necessary self-collection devices for non-invasive, at-home saliva collection, making it easy to deliver real-time, data-driven healthcare solutions without the need for lab visits.

ExtendingME Testing Kit
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