Real‐World Patient Eligibility for Alzheimer's Disease Anti‐Amyloid Therapy in Seven Swedish Memory Clinics
Open Access
- 20 October 2026
- journal article
- Published by Wiley in European Journal of Neurology
- Vol. 33 (10)
Abstract
Background: Anti‐amyloid therapies lecanemab and donanemab are the first potentially disease‐modifying treatments for Alzheimer's disease (AD) approved in Europe. We estimated real‐world eligibility for these treatments in a large multicenter memory clinic patient cohort in Sweden (MemClin). Methods: MemClin included patients with a first diagnostic visit between 2016 and 2022 at seven specialist memory clinics in Stockholm, Sweden. To estimate eligibility for anti‐amyloid therapy, we applied key inclusion/exclusion criteria from the lecanemab and donanemab appropriate use recommendations. Eligible patients were required to have (1) a clinical diagnosis of AD‐type dementia or mild cognitive impairment (MCI), (2) confirmed Aβ pathology (abnormal CSF Aβ42) and (3) no apparent medical exclusion criteria. Eligibility was calculated for different scenarios to provide both upper‐bound estimates (main analysis) and more conservative, implementation‐ready estimates of near‐term treatable patients (sensitivity analysis). Results: Cohort consisted of 2126 patients (mean age 77.1 ± 6.6 years; 61.8% MCI, 24.2% dementia, 13.7% subjective cognitive impairment). In the main analysis, 11.5% of the whole cohort was estimated to be eligible for either treatment (lecanemab 10.6%, donanemab 11.5%). Most eligible patients had early‐stage disease (61.9% MCI vs. 38.1% dementia) and an A + T– biomarker profile, that is, normal biomarker of tau (57.9%). Eligibility was markedly lower in sensitivity analyses (e.g., 2.7% when all patients without MRI were assumed ineligible). Conclusions: Even upper‐bound estimates indicate that a minority of real‐world memory clinic patients may currently qualify for anti‐amyloid therapy. These findings provide timely evidence to inform the ongoing debate on the implementation of anti‐amyloid therapy in public healthcare.Keywords
Funding Information
- Innovative Health Initiative (101112145)
- Innovative Health Initiative (101132933)
- Center for Innovative Medicine (FoUI‐104172)
- EU Joint Programme – Neurodegenerative Disease Research (357810)
- Alzheimerfonden (AF‐1031812)
- Vetenskapsrådet (2025‐02405)
- Konung Gustaf V:s och Drottning Victorias Frimurarestiftelse
- Hjärnfonden (FO2026‐0228)
- Forskningsrådet för hälsa, arbetsliv och välfärd (2025‐02071)
- VINNOVA (2025‐03749)
This publication has 29 references indexed in Scilit:
- Donanemab treatment effect by baseline tau burden and disease severity: Observations from the TRAILBLAZER‐ALZ 2 trialAlzheimer's & Dementia, 2026
- Eligibility for lecanemab and donanemab in Korea under Appropriate Use RecommendationsAlzheimer's & Dementia, 2025
- Lecanemab Treatment in a Specialty Memory ClinicJAMA Neurology, 2025
- “Real‐world” eligibility for anti‐amyloid treatment in a tertiary memory clinic settingAlzheimer's & Dementia, 2025
- Developing Treatment Models for the Delivery of the Antiamyloid Therapy, Lecanemab: Considerations for Implementation of Lecanemab in Healthcare SystemsThe American Journal of Geriatric Psychiatry, 2025
- Blood Biomarkers to Detect Alzheimer Disease in Primary Care and Secondary CareJAMA, 2024
- Projected Annual Lecanemab Treatment Eligibility in an Irish Regional Specialist Memory ClinicInternational Journal of Geriatric Psychiatry, 2024
- Donanemab in Early Symptomatic Alzheimer DiseaseJAMA, 2023
- Potential eligibility for Aducanumab therapy in an Irish specialist cognitive service—Utilising cerebrospinal fluid biomarkers and appropriate use criteriaInternational Journal of Geriatric Psychiatry, 2022
- Global estimates on the number of persons across the Alzheimer's disease continuumAlzheimer's & Dementia, 2022