Cited by 70Dementia and Cognitive Impairment ResearchAlzheimer's disease research and treatmentsCerebrospinal fluid and hydrocephalus

The DOI matches its Crossref record; the references it cites are not checked yet.

β-Amyloid, Tau, Neurodegeneration Classification and Eligibility for Anti-amyloid Treatment in a Memory Clinic Population

Open access

Abstract

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.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1212/wnl.0000000000201043

Cites

Statistics

Figures

Figure 1 Study Flowchart and Patient Selection. * CSF markers required for our study were Aβ42, Aβ42/40, and tau markers (p-tau and t-tau). Either one of the Aβ markers was missing for 7 patients; 1 patient did not have data on any Aβ or tau markers (only neurofilament light NfL available).
Figure 1 Study Flowchart and Patient Selection. * CSF markers required for our study were Aβ42, Aβ42/40, and tau markers (p-tau and t-tau). Either one of the Aβ markers was missing for 7 patients; 1 patient did not have data on any Aβ or tau markers (only neurofilament light NfL available).CC BY · PubMed Central

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

The citation lists haven’t been fetched yet

References 50 · Cited by 70

Research works printed but not linked: 40

  1. 10.1212/WNL.0000000000002923 · DOI · Paper page
  2. 10.1212/WNL.0000000000005476 · DOI
  3. 10.1159/000515322 · DOI
  4. 10.1002/alz.12292 · DOI
  5. 10.1038/s41598-018-26151-8 · DOI
  6. 10.14283/jpad.2019.25 · DOI
  7. 10.1186/s13195-021-00799-3 · DOI
  8. 10.1001/jama.2019.7437 · DOI · Paper page
  9. 10.1212/WNL.0000000000007248 · DOI
  10. 10.1212/WNL.0000000000008361 · DOI
  11. 10.3233/JAD-191227 · DOI
  12. 10.1212/WNL.0000000000009724 · DOI · Paper page
  13. 10.1186/s13195-020-00621-6 · DOI
  14. 10.1002/dad2.12026 · DOI
  15. 10.1002/dad2.12031 · DOI
  16. 10.14283/jpad.2021.41 · DOI · Paper page
  17. 10.1016/0022-3956(75)90026-6 · DOI · Paper page
  18. 10.1111/j.1532-5415.2005.53221.x · DOI · Paper page
  19. 10.1007/978-0-387-79948-3_4454 · DOI
  20. 10.1007/978-0-387-79948-3_1153 · DOI
  21. 10.1007/978-0-387-79948-3_1399 · DOI
  22. 10.1186/s13195-019-0550-8 · DOI
  23. 10.3389/fnagi.2021.604119 · DOI
  24. 10.1007/BF00868807 · DOI
  25. 10.1159/000117270 · DOI
  26. 10.1007/s00330-011-2205-4 · DOI
  27. 10.2214/ajr.149.2.351 · DOI
  28. 10.1007/s00330-019-06067-1 · DOI
  29. 10.3389/fnagi.2017.00117 · DOI
  30. 10.1373/clinchem.2017.281055 · DOI
  31. 10.1186/s13195-020-00713-3 · DOI
  32. 10.1212/WNL.0000000000009485 · DOI · Paper page
  33. 10.1001/jama.2021.15286 · DOI
  34. 10.1016/j.ijcard.2017.07.012 · DOI
  35. 10.1038/s41582-021-00520-w · DOI
  36. 10.1186/s13195-019-0485-0 · DOI · Paper page
  37. 10.1186/s13195-018-0362-2 · DOI
  38. 10.3233/jad-210236 · DOI
  39. 10.1186/s13195-015-0114-5 · DOI
  40. 10.1001/jama.2015.4668 · DOI · Paper page

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
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
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

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

How to cite

Cite CoChat for the checks on this page, and the paper for its own findings.

This page
CoChat. (2026). Citation check: β-Amyloid, Tau, Neurodegeneration Classification and Eligibility for Anti-amyloid Treatment in a Memory Clinic Population. https://app.cochat.ai/papers/10.1212/wnl.0000000000201043
The paper
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