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β-Amyloid, Tau, Neurodegeneration Classification and Eligibility for Anti-amyloid Treatment in a Memory Clinic Population
Open accessAbstract
BACKGROUND AND OBJECTIVES: ATN (β-amyloid [Aβ], tau, neurodegeneration) system categorizes individuals based on their core Alzheimer disease (AD) biomarkers. An important potential future use for ATN is therapeutic decision-making in clinical practice once disease-modifying treatments (e.g., anti-amyloid), become widely available. In this cross-sectional study, we applied ATN and estimated potential eligibility for anti-amyloid treatment in a real-life memory clinic with biomarker assessments integrated into the routine diagnostic procedure and all specialized resources available for the implementation of novel treatments. METHODS: We included all consecutive patients at the Karolinska University Hospital Memory clinic in Solna, Stockholm, Sweden, who had their first diagnostic visit in April 2018-February 2021, informed consent for the clinic research database, and available clinical and biomarker (CSF and imaging) data. ATN classification was based on CSF Aβ42 (or Aβ42/40; A), CSF phosphorylated tau (T), and medial temporal lobe atrophy (N). For CSF markers, we applied laboratory cutoffs and data-driven cutoffs for comparison (determined with Gaussian mixture modeling). Eligibility for anti-amyloid treatment was assessed following the published recommendations for aducanumab (AD dementia or mild cognitive impairment [MCI] with no evidence of non-AD etiology, appropriate level of cognition, and AD-consistent CSF profile). RESULTS: The study population consisted of 410 patients (52% subjective cognitive impairment, 23% MCI, and 25% any dementia; age 59 ± 7 years, 56% women). Regardless of biomarker cutoffs, most patients were A-T-N- (54%-57%). A+ prevalence was 17%-30% (higher with data-driven cutoffs). Up to 13% of all patients (27% of those with MCI and 28% of those with dementia) were potentially eligible for anti-amyloid treatment when AD-consistent CSF was defined as any A+ profile. When A+T+ profile was required, treatment was targeted more to the dementia than MCI stage (eligibility up to 14% in MCI and 22% in dementia). The opposite applied to earlier-stage intervention (A+T-N-; eligibility up to 12% in MCI and 2% in dementia). DISCUSSION: In a memory clinic setting with all necessary infrastructure and national guidelines in place for dementia diagnostic examination (best-case scenario), most of the patients did not meet the eligibility criteria for anti-amyloid treatment. Continuing the development of disease-modifying treatments with different mechanisms of action is a priority.
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“Alzheimer's disease (AD) is a progressive neurodegenerative disorder characterized by two core biomarkers: amyloid beta (Aβ) plaques and tau neurofibrillary tangles.”
From Unique transcriptomic alterations in 5XFAD;PS19 mouse model identify glial lipid dysregulation and coordinated microglial–oligodendrocyte responses (2026) · cites this paper as [1]
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Metadata
- Authors
- Rosenberg, A., Öhlund-Wistbacka, U., Hall, A., Bonnard, A., Hagman, G., Rydén, M., Thunborg, C., Wiggenraad, F., Sandebring-Matton, A., Solomon, A., & Kivipelto, M.
- Affiliations
- Karolinska University Hospital (SE)
- From the Division of Clinical Geriatrics (A.R., U.Ö.-W., C.T., A.S.-M., A.S., M.K.), Centre for Alzheimer Research, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden; Department of Neurology (A.R., A.H., A.S, M.K.), Institute of Clinical Medicine, University of Eastern Finland, Kuopio; Medical Unit Aging (U.Ö.-W., A.B., G.H., M.R., F.W., M.K.), Karolinska University Hospital, Stockholm, Sweden; Division of Neurogeriatrics (A.S.M.), Centre for Alzheimer...
- Corresponding author
- Rosenberg, Anna
- Venue
- Neurology
- Published
- 2022-11-08
- Volume
- 99
- Issue
- 19
- Pages
- e2102-e2113
- ISSN
- 0028-3878 (ISSN-L)
- 1526-632X
- PMC
- PMC9651451
- OpenAlex
- W4296714032
- Cited by
- 70
- References
- 50
- Citations by year
- 2026: 19 · 2025: 21 · 2024: 23 · 2023: 7
- FWCI
- 8.31
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- cc-by
- Locations
- Neurology (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- H2020 European Research Council (804371)
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Alzheimer's disease research and treatments
- Health Sciences › Medicine › Clinical Neurology › Cerebrospinal fluid and hydrocephalus
- Keywords
- Alzheimer's disease, aducanumab, amyloid-beta, phosphorylated tau, medial temporal lobe atrophy, cerebrospinal fluid biomarkers, mild cognitive impairment, dementia, memory clinic patients, biomarker cut-off values, disease-modifying therapy, early intervention, Gaussian mixture model, amyloid PET, FDG-PET
- MeSH terms
- Aged, Alzheimer Disease, Amyloidosis, Cross-Sectional Studies, Female, Humans, Male, Middle Aged, Peptide Fragments, Biomarkers, Amyloid beta-Peptides, tau Proteins, Disease Progression, Cognitive Dysfunction
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- Rosenberg, A., Öhlund-Wistbacka, U., Hall, A., Bonnard, A., Hagman, G., Rydén, M., Thunborg, C., Wiggenraad, F., Sandebring-Matton, A., Solomon, A., & Kivipelto, M. (2022). β-Amyloid, Tau, Neurodegeneration Classification and Eligibility for Anti-amyloid Treatment in a Memory Clinic Population. Neurology. https://doi.org/10.1212/wnl.0000000000201043