amyloid-related imaging abnormality-edema, effusions, hemorrhage or siderosis (ARIA-E, ARIA-H)

From Aaushi
Jump to navigation Jump to search

Etiology

* 2-3% of placebo recipients in aducanumab clinical trial with ARIA-E

* incidence dose-related[3]

Pathology

Genetics

Clinical manifestations

Radiology

  • abnormalities seen on MRI neuroimaging*
    • 98% resolve, 83% within 16 weeks (weeks)

Management

More general terms

References

  1. George J Alzheimer's Drug Slows Decline, Trial Data Show. Lecanemab met primary and secondary endpoints, but was associated with adverse events. MedPage Today November 30, 2022 https://www.medpagetoday.com/neurology/alzheimersdisease/101972
    van Dyck CH, Swanson CJ, Aisen P Lecanemab in Early Alzheimer's Disease. N Engl J Med 2022. Nov 29. PMID: https://www.ncbi.nlm.nih.gov/pubmed/36449413 https://www.nejm.org/doi/full/10.1056/NEJMoa2212948
  2. 2.0 2.1 2.2 Salloway S, Chalkias S, Barkhof F et al Amyloid-Related Imaging Abnormalities in 2 Phase 3 Studies Evaluating Aducanumab in Patients With Early Alzheimer Disease. JAMA Neurol. 2022 Jan 1;79(1):13-21. PMID: https://www.ncbi.nlm.nih.gov/pubmed/34807243 PMCID: PMC8609465 Free PMC article. Clinical Trial.
  3. 3.0 3.1 Filippi M, Cecchetti G, Spinelli EG, Vezzulli P, Falini A, Agosta F. Amyloid-Related Imaging Abnormalities and beta-Amyloid-Targeting Antibodies: A Systematic Review. JAMA Neurol. 2022 Mar 1;79(3):291-304 PMID: https://www.ncbi.nlm.nih.gov/pubmed/35099507 Review. https://jamanetwork.com/journals/jamaneurology/fullarticle/2788269