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This page is alzhub.org's plain-English summary of a published study, not the paper itself. It is generated from the record we hold for this study, sourced and linked below — check the original for the full text and methods.

⚠ Preprint — not yet peer-reviewed alzhub usefulness score 16 out of 100. Treatments

Topic: Plasma and spinal-fluid biomarkers

Background The benefits of amyloid-β monoclonal antibodies for Alzheimer’s disease are tempered by the risk of amyloid-related imaging abnormalities (ARIA). Detailed real-world characterization of ARIA, including incidence, timing, radiologic severity and localization, natural history, and risk factors, is essential to optimize treatment safety. This study provides a comprehensive description of ARIA in a large real-world cohort of patients receiving lecanemab. Methods In this retrospective cohort study from the Mass General Brigham Alzheimer’s Therapeutic Program, we analyzed data from 468 patients with early Alzheimer’s disease who were at least 90 days from their first lecanemab infusion, including those whose treatment was modified or discontinued. ARIA was monitored using a standardized MRI protocol. High-dimensional analysis of baseline clinical, laboratory, and biomarker variables was performed using univariate correlations and Cox proportional hazards models with data-driven cutpoints. Findings The overall incidence of any ARIA was 25.2%, with ARIA-H occurring in 22.4% of patients and ARIA-E in 12.2%. Symptoms developed in 4.5% of all patients. Both subtypes demonstrated significant occipital involvement, with ARIA-H showing additional frontotemporal predominance. ARIA-H was typically mild and persistent with rare radiologic resolution, whereas ARIA-E was transient, resolving with a mean time to resolution of 75.6 days. Key baseline predictors of ARIA-H included CSF Aβ42 ≤683.8 pg/mL (HR 6.39), ≥1 microhemorrhage (HR 2.55), and at least one APOE ε4 allele (HR 1.77). ARIA-E was predicted by diastolic blood pressure >75 mmHg (HR 3.12), serum chloride >105 mmol/L (HR 2.79), at least one APOE ε4 allele (HR 2.51), and serum sodium >141 mmol/L (HR 1.70). ARIA-Mixed was associated with elevated serum chloride >105 mmol/L (HR 3.92), at least one APOE ε4 allele (HR 2.87), and diastolic blood pressure >75 mmHg (HR 2.60). Interpretation This comprehensive real-world characterization of ARIA, together with the identification of novel modifiable risk factors for ARIA-E, including elevated diastolic blood pressure and high-normal serum electrolytes, enables personalized risk assessment and tailored monitoring, thereby advancing the safe implementation of disease-modifying Alzheimer’s therapies. Funding Funding for this project was provided by the Mass General Neuroscience Transformative Scholar Award.

Cite this study APA, Vancouver, BibTeX · download .bib or .ris

APA 7th

Rezaii, N., Dickson, JR., Ford, J. N., He, Y., Katsumi, Y., Ramirez-Gomez, L., et al. (2026). Real-World Characterization of Amyloid-Related Imaging Abnormalities (ARIA) in Lecanemab Treatment at an Academic Health System. medRxiv. https://doi.org/10.64898/2026.01.23.26344739

Vancouver

Rezaii N, Dickson JR, Ford JN, He Y, Katsumi Y, Ramirez-Gomez L, et al. Real-World Characterization of Amyloid-Related Imaging Abnormalities (ARIA) in Lecanemab Treatment at an Academic Health System. medRxiv. 2026. doi:10.64898/2026.01.23.26344739.

BibTeX

@article{rezaii2026-4202aa20,
  author  = {Rezaii, N. and Dickson, JR. and Ford, J. N. and He, Y. and Katsumi, Y. and Ramirez-Gomez, L. and Lam, A. and Shah, H. and others},
  title   = {{Real-World Characterization of Amyloid-Related Imaging Abnormalities (ARIA) in Lecanemab Treatment at an Academic Health System}},
  journal = {medRxiv},
  year    = {2026},
  doi     = {10.64898/2026.01.23.26344739},
  url     = {https://doi.org/10.64898/2026.01.23.26344739}
}

Built from the record alzhub holds for this paper, not looked up. Volume, issue and page numbers are not held in the record. The record's author list ends in “et al.”, so not every author is named. Check the citation against the original before you use it.

Key findings

Study details

How this study scored 16/100
How this study's score is builtJournal tier 2 of 10; Journal's citation record 0 of 4; Study design 7 of 12; Strength of evidence 3 of 5; Peer-review validation 4 of 10; How recent 5 of 5; Sample size 2 of 4; Effect reported 2 of 3; Studied in people 3 of 3; Randomised / blinded 0 of 2; Times cited left out, no data; Citations per year left out, no data; Impact for its field and year left out, no data; Cited by studies here left out, no data; Still being cited left out, no data; Senior author's track record left out, no data; Institution's track record left out, no data; Multi-centre collaboration left out, no data; Indexed in PubMed 1 of 2; Free to read 0 of 2. 29 of the 62 points it could be judged on, which is 47 of 100. Raw total 47 of 100, shown as 16 because this is not a peer-reviewed research article.raw total 47 of 100capped at 16 — hatched points do not count

Preprint — not yet peer-reviewed. It scored 47 on the same rubric, but non-peer-reviewed sources are capped at 16, so it shows as 16. Scored zero for randomised / blinded because the record does not state it. We have no data on times cited, citations per year, impact for its field and year, cited by studies here, still being cited, senior author's track record, institution's track record and multi-centre collaboration, so those were left out: it earned 29 of the 62 points we could judge it on, which is 47 out of 100.

ComponentPointsWhy
Journal tier 2 / 10 Tier 4 — not a peer-reviewed journal (medRxiv)
Journal's citation record 0 / 4 Not a journal article, so the journal's record does not count
Study design 7 / 12 A cohort study following people over time
Strength of evidence 3 / 5 Rated “moderate” in our summary
Peer-review validation 4 / 10 Preprint — not yet peer-reviewed. Hosted on a preprint server.
How recent 5 / 5 2026 — within 1 year(s) of the newest study here
Sample size 2 / 4 468 participants
Effect reported 2 / 3 Effect reported as a number, without an interval or test
Studied in people 3 / 3 Studied in people (participant count stated)
Randomised / blinded 0 / 2 No randomisation or blinding stated — scores zero (not stated in the record — scored 0)
Times cited — / 7 No citation count (not found in OpenAlex) — left out of this score
Citations per year — / 5 No citation count or no year — left out of this score
Impact for its field and year — / 6 No field-weighted citation impact (OpenAlex has none yet) — left out of this score
Cited by studies here — / 6 Not yet checked against this library's citation graph — left out of this score
Still being cited — / 4 No yearly citation counts — left out of this score
Senior author's track record — / 4 Senior author's record not available — left out of this score
Institution's track record — / 3 No institution listed in OpenAlex — left out of this score
Multi-centre collaboration — / 3 Institutions not listed — left out of this score
Indexed in PubMed 1 / 2 Not in PubMed, but has a DOI
Free to read 0 / 2 Behind a paywall — scores zero
Points 29 / 62 Scored on 12 of 20 parts. We have no data for the rest, so they are left out: 29 of the 62 points we could judge it on is 47 out of 100.
Total 47 / 100 Capped to 16 because this is not a peer-reviewed article.

What each of these 20 components measures, and what this score is not →

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