$195
Unlock insights into your genetic risk for late-onset Alzheimer’s disease. Our easy-to-use DNA test kit identifies the presence of the APOE e4 variant, a key indicator linked to increased chances of developing late-onset Alzheimer’s.
Alzheimer’s is a progressive disorder that affects the brain, impairing memory and essential mental functions. It’s the main cause of dementia worldwide, being responsible for 60–70% of around 55 million global dementia cases as of 2023.
Most Alzheimer’s patients exhibit symptoms after age 65, referred to as late-onset Alzheimer’s disease. This type comprises over 90% of all cases. A rarer type, “early-onset”, can appear before age 65 and is often hereditary.
Alzheimer’s is a neurodegenerative disease, meaning it involves the gradual degeneration or death of brain cells. The first alterations in the brain start well before any recognizable symptoms appear.
The hallmark of Alzheimer’s is the formation of two distinct protein abnormalities:
Alzheimer’s disease, a progressive brain disorder, primarily affects memory and thinking skills. While symptoms can vary among individuals, there are common indicators that might suggest the onset or progression of the disease:
Variation in the APOE gene is the strongest genetic factor influencing the risk of late-onset Alzheimer’s disease. This gene plays an important role in the body including transporting fats, supporting neuronal growth and nerve regeneration, regulating immune responses, and repairing injuries in the central nervous system.
The APOE gene has three common alleles: e2, e3, and e4. Everyone has two copies of this gene, which combine in pairs to influence their Alzheimer’s disease risk:
Understanding your APOE gene variant helps in early detection and intervention. Early action, including monitoring and medication, can slow down the progression of Alzheimer’s disease. Knowing your risk promotes informed healthcare decisions.
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