Neurodegeneration
How safe is clinic lecanemab in practice?
Open access · cc by · source: Europe PMC
Among 234 memory-clinic patients on lecanemab, infusion reactions (37%) and ARIA (22%) were common but generally manageable; mild dementia had much higher symptomatic ARIA.
Study at a glance
- Design
- Cohort — Retrospective consecutive case series of specialty-clinic lecanemab initiations
- N
- N=234 · Patients with early symptomatic AD receiving ≥1 infusion
- Population
- Early symptomatic Alzheimer disease patients at Washington University Memory Diagnostic Center
- Outcome
- Infusion reactions, ARIA (including symptomatic), and treatment withdrawal
Structured fields used in claim comparison tables when every cited study has a complete layer.
Key findings
IRR 37%; ARIA 22% (ARIA-E 15%, isolated ARIA-H 6.7%); symptomatic ARIA 5.7% overall but 27% in mild dementia vs 1.8% in MCI/very mild; 9.8% withdrew (4.3% for ARIA); no macrohemorrhage/death.
Methodology
Reviewed consecutive lecanemab starts (Aug 2023–Oct 2024), dosing every 2 weeks, MRI monitoring, and adverse events through Dec 2024.
Limitations
Long-term efficacy vs placebo in this clinic sample, or risk under every eligibility exception.
How this study connects
Role on claims
Each row is a claim on a concept or method page where this paper supports, challenges, or qualifies the statement. Roles are hand-checked — not a model guess.
Brain multi-omics reveals multimodal AD molecular profiles including a severe cluster.
Integrating transcriptomic/proteomic/metabolomic/lipidomic brain data yielded four multimodal profiles, including Knight-C4 with pronounced dysregulation and worse clinical features.
Scope note — clinic anti-amyloid treatment experience — not a multi-omics subtype discovery
Limits the claim's scope: a different population, assay, or outcome.
Specialty clinics are delivering lecanemab with real-world workflow constraints.
A specialty memory-clinic report on lecanemab treatment adds practice-level evidence beside biomarker/pathology marker papers.
Evidence for the claim as stated.
History
When this study was placed
Dated entries from the concept change log — when this paper was added or removed as support, challenge, or qualifier on a claim.
Placed as a scope qualifier on Alzheimer’s and MCI markers
Integrating transcriptomic/proteomic/metabolomic/lipidomic brain data yielded four multimodal profiles, including Knight-C4 with pronounced dysregulation and worse clinical features.
Placed as supporting evidence on Alzheimer’s and MCI markers
A specialty memory-clinic report on lecanemab treatment adds practice-level evidence beside biomarker/pathology marker papers.
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