ApoE Status Report

Overview

APOE Status Report

What This Test Covers

APOE Genotype Analysis

Determines the individual's APOE genotype based on the two defining SNPs

These variants identify the three major APOE isoforms:

APOE Status & Risk Interpretation

Provides a clear genetic risk classification based on APOE genotype

This interpretation supports provider-led risk assessment and preventive care planning.

Comprehensive APOE Genotype Interpretation

Includes a detailed interpretation table outlining

Personalized Brain Health Support

The report provides evidence-informed recommendations across

Why It Matters

APOE is one of the most extensively studied genetic markers associated with cognitive aging and lipid metabolism. While genotype alone does not determine whether disease will occur, it can provide valuable insight into inherited biological susceptibility.

Understanding APOE status enables healthcare professionals to identify individuals who may benefit from earlier monitoring, personalized preventive interventions, and targeted lifestyle strategies that support long-term brain and cardiometabolic health.

Rather than waiting for symptoms to emerge, clinicians can use APOE status to deliver more proactive, precision-guided care.

Who Should Take This Test

The APOE Status Report is designed for

Physicians and neurologists

Functional & integrative medicine practitioners

Preventive and longevity-focused clinicians

Cardiovascular specialists

Healthcare professionals supporting patients with cognitive concerns or a family history of Alzheimer's disease

What You’ll Receive

ExtendingME Lab Analysis

Comprehensive Report

A clean report layout with with APOE genotype determination (ε2, ε3, ε4), APOE status and genetic risk interpretation, and a comprehensive genotype interpretation table.

Your Journey Begins

Personalized Insights

Personalized nutrition insights, lifestyle recommendations, cognitive exercise training guidance, and brain health education.

Continued Education

Provider Portal Access

Secure digital report access via the ExtendingME Provider Portal for seamless report viewing and sharing.

Why Epigenetic Testing is Important

SNP-Specific Risk Interpretations

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

Congenital Disease Risk Management

Turnaround Time

Results are available within 2 weeks from sample receipt and are securely delivered through the Provider Portal for convenient clinical review and patient follow-up.

Collection Method

ExtendingME kits include everything required for convenient, non-invasive saliva collection. Samples can be collected from home and returned for laboratory analysis, providing a simple and accessible approach to genetic testing.

ExtendingME Testing Kit

Meet EMma Soft —
Powering Personalized Medicine

EMma Soft is ExtendingME’s proprietary platform designed to connect every part of your personalized medicine offering—from genetic insights to patient engagement and ongoing care. It brings your entire ecosystem together to support scalable growth and long-term value.

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