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WHAT IS ARIA?
- Amyloid-Related Imaging Abnormalities (ARIA) are side effects that may occur in patients receiving monoclonal antibody intravenous infusions for Alzheimer’s disease.
- ARIA is detected through brain imaging (MRI) and is categorized into two types:
- ARIA-E (Edema): Swelling in the brain.
- ARIA-H (Hemosiderin deposition): Small areas of bleeding in the brain.
WHY GENETIC TESTING MATTERS
- Knowing your ApoE 4 status can help your healthcare provider evaluate your risk of ARIA and guide treatment decisions.
- The risk of ARIA varies depending on your genetic profile and other factors. The ApoE ε4 gene plays a significant role:
- ApoE 4 Homozygote (two copies of E4 allele):
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- Approximately 30-40% of patients may experience ARIA, with most cases being asymptomatic or mild.
- ApoE 4 Heterozygote (one copy of the E4 allele):
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- Around 20-25% of patients may experience ARIA.
- Non-carriers (no copies of Apo E4 allele):
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- About 10-15% of patients may experience ARIA.
ARIA SEVERITY
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- Rare - occurs in approximately 1-2% of patients.
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- More likely in ApoE ε4 homozygotes.
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- More Common - occurs in approximately 10-20% of patients.
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- Often detected on MRI without symptoms.
SYMPTOMS OF ARIA
- Most ARIA cases have no symptoms.
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- Occurs in 5-10% of patients.
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- Call your provider promptly if you experience any of these symptoms.
ARIA MANAGEMENT
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- Routine MRI scans are conducted before starting treatment and periodically during therapy to detect ARIA early.
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- If ARIA is detected, your doctor may temporarily stop or adjust the treatment dosage.
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- Symptomatic ARIA may require additional medical interventions to alleviate symptoms.
KEY TAKEAWAYS
- ARIA is a potential side effect of monoclonal antibody treatments for Alzheimer’s disease.
- Discuss risks and benefits with your provider. Risks and benefits are based your ApoE ε4 genetic profile and overall health.
- Regular monitoring and prompt communication with your healthcare provider ensure the best outcomes.