Alzheimer's Panel

Overview

Alzheimer’s disease is a progressive neurodegenerative disorder that impacts memory, cognition, and quality of life. Today, an estimated 6.9 million Americans aged 65 and older are living with Alzheimer’s dementia, a number projected to rise to 13.8 million by 2060. While symptoms often emerge later in life, the underlying biological changes begin decades earlier.

By analyzing a broad range of gene variants, this panel helps identify risk before symptoms arise empowering both providers and patients to take proactive steps.

What This Test Covers

Our Panel is structured into six key categories, each addressing distinct pathways that influence Alzheimer’s disease risk and cognitive health:

Neurodegenerative Risk Genetics

Microbiome–Cognitive Health Profile

Alzheimer’s Metabolic Risk Indicators

Homocysteine Regulation

Neuro-Immune Health

Nutrient Metabolism Profiles

Why It Matters

Early detection of genetic risk can be a game-changer allowing for preventive strategies that delay or reduce disease progression. The Alzheimer’s Panel helps address this urgency by offering:

Who Should Take This Test

This panel is ideal for:

Adults with a family history of Alzheimer’s or dementia seeking proactive risk assessment.

Individuals experiencing early signs of cognitive decline or memory concerns

Functional and integrative medicine practitioners addressing brain aging at the root.

Neurologists and dementia clinics integrating genomics into diagnostic protocolssing cutting-edge genetic data.

Providers supporting patients with brain fog, emotional changes, or mood shifts

Anyone seeking to personalize brain health plans with precision-based insights

What You’ll Receive

Comprehensive Genetic Report

Organized into clear categories and subcategories, covering key health areas.

Your Journey Begins.

Personalized Insights

Actionable insights for nutrition, lifestyle, labs to consider and supplementation based on patients' unique genetic profile.

Continued Education

Provider Portal Access

Results are delivered digitally through the ExtendingME Provider Portal, ensuring seamless viewing, and sharing of reports.

Why Epigenetic Testing is Important

SNP-Specific Risk Interpretations (optional, based on your requirements)

For providers seeking deeper genetic insights, we offer detailed SNP-level interpretations.

Congenital Disease Risk Management

Turnaround Time

Results will be available within 3 weeks from the receipt of the sample and will be securely delivered through the Provider Portal, enabling seamless access, viewing, and sharing of reports.

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.

Take Action Before Symptoms Start

Early genetic insights. Smarter prevention. Personalized brain health powered by your DNA

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