Assessing Eligibility for Anti‐Amyloid Treatment Among Primary Care Patients with Cognitive Symptoms
(2025) In Alzheimer's & dementia : the journal of the Alzheimer's Association- Abstract
- Background
Primary care is key to early identification and referral of patients with Alzheimer’s disease (AD). Assessing eligibility for new anti-amyloid treatment may guide appropriate referrals and prevent overburdening specialized care. In this study we determined eligibility for anti-amyloid treatment in patients undergoing cognitive evaluation in primary care.
Method
Patients were selected from the BioFINDER-Primary Care study (NCT06120361), which consecutively enrolls patients undergoing cognitive evaluation at 25 primary care units in Sweden. Between January 2020 and April 2025, patients were comprehensively assessed for co-morbidities, treatments, clinical symptoms, and cognitive status. Eligibility for... (More) - Background
Primary care is key to early identification and referral of patients with Alzheimer’s disease (AD). Assessing eligibility for new anti-amyloid treatment may guide appropriate referrals and prevent overburdening specialized care. In this study we determined eligibility for anti-amyloid treatment in patients undergoing cognitive evaluation in primary care.
Method
Patients were selected from the BioFINDER-Primary Care study (NCT06120361), which consecutively enrolls patients undergoing cognitive evaluation at 25 primary care units in Sweden. Between January 2020 and April 2025, patients were comprehensively assessed for co-morbidities, treatments, clinical symptoms, and cognitive status. Eligibility for anti-amyloid treatment was evaluated based on Cummings et.al (2023). MRI was assessed by a senior neuroradiologist. Amyloid status was determined using cerebrospinal fluid (CSF) Aβ42/40 ratio or amyloid PET. All patients received a full clinical work-up at a specialized memory clinic.
Result
A total of 636 participants were examined. The prevalence of treatment contraindications is presented in Table 1. 35 individuals had contraindications for MRI and were excluded. From the remainder, 386 (60.7%) participants had treatment-appropriate cognitive status (mild cognitive impairment or mild dementia) and among these, 226 (35.5%) were amyloid positive. Of these, 37 were considered to have a non-AD etiology for their symptoms, leaving 189 for further evaluation. After excluding patients with significant comorbidities (active anticoagulant treatment, immunological disease, cancer, stroke/TIA within 12 months, or epilepsy) 124 (19.5%) remained. Excluding those with MRI abnormalities reduced the sample to 74 (11.6%). Additional exclusion criteria (BMI and age restriction) reduced the eligible participant group to 71 (11.2%). Finally, applying the EMA, but not FDA, restriction excluding APOE ε4 homozygotes (11 remaining individuals) resulted in an eligible population of 60 individuals (9.4%) (Figure 1).
Conclusion
About 9-11% of patients undergoing cognitive evaluation in primary care are potentially eligible for anti-amyloid treatment under current clinical guidelines. Major exclusion factors included neuroimaging findings, anticoagulant use, and comorbidities. These findings may guide expectations around treatment uptake and support real-world health-economic analyses based on patient eligibility. At AAIC, we will present a proposed workflow to streamline identification of treatment candidates from primary to specialist care.
(Less)
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https://lup.lub.lu.se/record/d245213a-32e8-4c7e-9814-d906441f7cd0
- author
- Barbosa Djärf, Josef
LU
; Borgström Bolmsjö, Beata
LU
; van Westen, Danielle
LU
; Tideman, Pontus
LU
; Smith, Ruben
LU
; Schindler, Suzanne E.
; Mattsson-Carlgren, Niklas
LU
; Stomrud, Erik
LU
; Hansson, Oskar
LU
and Palmqvist, Sebastian
LU
- contributor
- Fawad, Ayesha
LU
- organization
-
- Clinical Memory Research (research group)
- MultiPark: Multidisciplinary research on neurodegenerative diseases
- Family Medicine and Community Medicine (research group)
- LU Profile Area: Proactive Ageing
- Neuroradiology (research group)
- Translational Diabetes Research (research group)
- Regeneration in Movement Disorders (research group)
- Brain Injury After Cardiac Arrest (research group)
- alternative title
- Bedömning av lämplighet för anti-amyloidbehandling hos primärvårdspatienter med kognitiva symtom
- publishing date
- 2025-12-23
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Alzheimer's & dementia : the journal of the Alzheimer's Association
- publisher
- Wiley
- ISSN
- 1552-5279
- DOI
- 10.1002/alz70861_108336
- language
- English
- LU publication?
- yes
- id
- d245213a-32e8-4c7e-9814-d906441f7cd0
- date added to LUP
- 2026-03-26 14:58:19
- date last changed
- 2026-03-26 15:46:21
@misc{d245213a-32e8-4c7e-9814-d906441f7cd0,
abstract = {{Background<br/>Primary care is key to early identification and referral of patients with Alzheimer’s disease (AD). Assessing eligibility for new anti-amyloid treatment may guide appropriate referrals and prevent overburdening specialized care. In this study we determined eligibility for anti-amyloid treatment in patients undergoing cognitive evaluation in primary care.<br/><br/>Method<br/>Patients were selected from the BioFINDER-Primary Care study (NCT06120361), which consecutively enrolls patients undergoing cognitive evaluation at 25 primary care units in Sweden. Between January 2020 and April 2025, patients were comprehensively assessed for co-morbidities, treatments, clinical symptoms, and cognitive status. Eligibility for anti-amyloid treatment was evaluated based on Cummings et.al (2023). MRI was assessed by a senior neuroradiologist. Amyloid status was determined using cerebrospinal fluid (CSF) Aβ42/40 ratio or amyloid PET. All patients received a full clinical work-up at a specialized memory clinic.<br/><br/>Result<br/>A total of 636 participants were examined. The prevalence of treatment contraindications is presented in Table 1. 35 individuals had contraindications for MRI and were excluded. From the remainder, 386 (60.7%) participants had treatment-appropriate cognitive status (mild cognitive impairment or mild dementia) and among these, 226 (35.5%) were amyloid positive. Of these, 37 were considered to have a non-AD etiology for their symptoms, leaving 189 for further evaluation. After excluding patients with significant comorbidities (active anticoagulant treatment, immunological disease, cancer, stroke/TIA within 12 months, or epilepsy) 124 (19.5%) remained. Excluding those with MRI abnormalities reduced the sample to 74 (11.6%). Additional exclusion criteria (BMI and age restriction) reduced the eligible participant group to 71 (11.2%). Finally, applying the EMA, but not FDA, restriction excluding APOE ε4 homozygotes (11 remaining individuals) resulted in an eligible population of 60 individuals (9.4%) (Figure 1).<br/><br/>Conclusion<br/>About 9-11% of patients undergoing cognitive evaluation in primary care are potentially eligible for anti-amyloid treatment under current clinical guidelines. Major exclusion factors included neuroimaging findings, anticoagulant use, and comorbidities. These findings may guide expectations around treatment uptake and support real-world health-economic analyses based on patient eligibility. At AAIC, we will present a proposed workflow to streamline identification of treatment candidates from primary to specialist care.<br/><br/>}},
author = {{Barbosa Djärf, Josef and Borgström Bolmsjö, Beata and van Westen, Danielle and Tideman, Pontus and Smith, Ruben and Schindler, Suzanne E. and Mattsson-Carlgren, Niklas and Stomrud, Erik and Hansson, Oskar and Palmqvist, Sebastian}},
issn = {{1552-5279}},
language = {{eng}},
month = {{12}},
note = {{Conference Abstract}},
publisher = {{Wiley}},
series = {{Alzheimer's & dementia : the journal of the Alzheimer's Association}},
title = {{Assessing Eligibility for Anti‐Amyloid Treatment Among Primary Care Patients with Cognitive Symptoms}},
url = {{http://dx.doi.org/10.1002/alz70861_108336}},
doi = {{10.1002/alz70861_108336}},
year = {{2025}},
}