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Vascular Considerations for Patients Receiving Amyloid Immunotherapy
S. Greenberg. Innovation in Aging, 2025-12-01
Topic: Amyloid, tau and blood-test diagnosis
Abstract Amyloid-related imaging abnormalities (ARIA) in the form of edema/effusions (ARIA-E) or hemorrhagic lesions (ARIA-H) are the most impactful adverse event associated with anti-amyloid immunotherapy for Alzheimer disease. Most ARIA events are mild or silent, but a small subset can be severely symptomatic or fatal. The pathophysiologic mechanisms for ARIA appear centered around interactions of β-amyloid peptide (Aβ) with the cerebrovasculature as it transits from plaques to the perivascular space or through direct antibody-Aβ interactions after deposition in arterioles as cerebral amyloid angiopathy (CAA). The key role of the vasculature in generating ARIA creates challenges for vascular clinicians, including safety of immunotherapy for individuals with CAA markers, whether immunotherapy-treated patients can also receive anticoagulants or thrombolytics, and treatment of severe ARIA. Among key vascular that have emerged from clinical trial data and adverse event reports are that 1) knowledge about ARIA should be disseminated throughout clinical teams providing stroke care, 2) ARIA risk can be stratified by pretreatment markers of CAA and incorporated into risk-benefit discussions, 3) the suggestive link between elevated blood pressure and ARIA risk supports close adherence to hypertension guidelines, 4) concomitant anticoagulation may increase risk of symptomatic ARIA-H and therefore requires considerable caution, 5) particular vigilance is required to avoid administering thrombolytics to patients with ARIA-E presenting as a stroke mimic, which has resulted in several fatalities, and 6) in addition stopping antibody infusion, high-dose corticosteroids can be considered for treatment of severe ARIA. These vascular considerations will likely evolve with ongoing post-marketing data collection efforts.
Key findings
- Abstract Amyloid-related imaging abnormalities (ARIA) in the form of edema/effusions (ARIA-E) or hemorrhagic lesions (ARIA-H) are the most impactful adverse event associated with anti-amyloid immunotherapy for Alzheimer disease.
Why it matters
This review describes ARIA as the most impactful adverse event of anti-amyloid immunotherapy and discusses vascular issues such as CAA markers, anticoagulant and thrombolytic safety, and treatment of severe ARIA. It addresses risk management rather than curing or preventing Alzheimer's disease.
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Study details
- Evidence strengthLow
How this study scored 29/100
Published in a peer-reviewed journal. Scored zero for study design, sample size, effect reported, studied in people and randomised / blinded because the record does not state it. We have no data on senior author's track record, so that was left out: it earned 28 of the 96 points we could judge it on, which is 29 out of 100.
| Component | Points | Why |
|---|---|---|
| Journal tier | 7 / 10 | Tier 3 — peer-reviewed journal (Innovation in Aging) |
| Journal's citation record | 0 / 4 | Innovation in Aging: journal h-index 48 (OpenAlex, 2026-10-29) |
| Study design | 0 / 12 | No study design recorded — scores zero, not guessed (not stated in the record — scored 0) |
| Strength of evidence | 1 / 5 | Rated “low” in our summary |
| Peer-review validation | 10 / 10 | Peer-reviewed. Published as an article in a named peer-reviewed journal. |
| How recent | 4 / 5 | 2025 — within 3 year(s) of the newest study here |
| Sample size | 0 / 4 | Participant count not stated — scores zero (not stated in the record — scored 0) |
| Effect reported | 0 / 3 | No effect size reported — scores zero (not stated in the record — scored 0) |
| Studied in people | 0 / 3 | Not stated whether this was studied in people — scores zero (not stated in the record — scored 0) |
| Randomised / blinded | 0 / 2 | No randomisation or blinding stated — scores zero (not stated in the record — scored 0) |
| Times cited | 0 / 7 | Cited 0 times (OpenAlex, 2026-10-10) |
| Citations per year | 0 / 5 | 0.0 citations a year over 3 year(s) since 2025 |
| Impact for its field and year | 0 / 6 | Cited 0.0× the average for papers of its field and year (OpenAlex FWCI) |
| Cited by studies here | 0 / 6 | No other study in this library cites it |
| Still being cited | 0 / 4 | Cited 0 times in 2024–2026 (2026 still in progress; OpenAlex) |
| Senior author's track record | — / 4 | OpenAlex's profile for last-listed author S. Greenberg holds only 4 work(s), too few to judge a track record — left out of this score |
| Institution's track record | 3 / 3 | Harvard University: institution h-index 3,235 (OpenAlex) |
| Multi-centre collaboration | 0 / 3 | OpenAlex lists 1 institution(s) in 1 country — scores zero (affiliation lists can be incomplete) |
| Indexed in PubMed | 1 / 2 | Not in PubMed, but has a DOI |
| Free to read | 2 / 2 | Free to read |
| Points | 28 / 96 | Scored on 19 of 20 parts. We have no data for the rest, so they are left out: 28 of the 96 points we could judge it on is 29 out of 100. |
| Total | 29 / 100 | — |
What each of these 20 components measures, and what this score is not →
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Cite this study APA, Vancouver, BibTeX · download .bib or .ris
Built from the record alzhub holds for this paper, not looked up. Volume, issue and page numbers are not held in the record. Check the citation against the original before you use it.
APA 7th
Greenberg, S. (2025). Vascular Considerations for Patients Receiving Amyloid Immunotherapy. Innovation in Aging. https://doi.org/10.1093/geroni/igaf122.1009
Vancouver
Greenberg S. Vascular Considerations for Patients Receiving Amyloid Immunotherapy. Innovation in Aging. 2025. doi:10.1093/geroni/igaf122.1009.
BibTeX
@article{greenberg2025-74e40508,
author = {Greenberg, S.},
title = {{Vascular Considerations for Patients Receiving Amyloid Immunotherapy}},
journal = {Innovation in Aging},
year = {2025},
doi = {10.1093/geroni/igaf122.1009},
url = {https://doi.org/10.1093/geroni/igaf122.1009}
}