Evidence map›Paper›PMID 36130840›Full record

ArticleNeurology2022

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

Anna Rosenberg, Ulf Öhlund-Wistbacka, Anette Hall, Alexandre Bonnard, Göran Hagman, Marie Rydén, Charlotta Thunborg, Fleur Wiggenraad, Anna Sandebring-Matton, Alina Solomon and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Neurology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 2 pooled it
8.1field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

50 citing papers in PubMed, 2 syntheses or guidelines pooled it, 59 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Observational
  14. Low number of patients qualifying for amyloid targeting immunotherapy.The journal of prevention of Alzheimer's disease · 2026
    Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 1 institution in 2 countries.

Anna RosenbergFrom 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 Research, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden; Ageing Epidemiology Research Unit, School of Public Health, Imperial College London, United Kingdom. anna.rosenberg@ki.se.ORCID 0000-0003-1456-7991
Ulf Öhlund-WistbackaFrom 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 Research, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden; Ageing Epidemiology Research Unit, School of Public Health, Imperial College London, United Kingdom.
Anette HallFrom 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 Research, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden; Ageing Epidemiology Research Unit, School of Public Health, Imperial College London, United Kingdom.
Alexandre BonnardFrom 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 Research, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden; Ageing Epidemiology Research Unit, School of Public Health, Imperial College London, United Kingdom.
Göran HagmanFrom 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 Research, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden; Ageing Epidemiology Research Unit, School of Public Health, Imperial College London, United Kingdom.
Marie RydénFrom 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 Research, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden; Ageing Epidemiology Research Unit, School of Public Health, Imperial College London, United Kingdom.
Charlotta ThunborgFrom 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 Research, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden; Ageing Epidemiology Research Unit, School of Public Health, Imperial College London, United Kingdom.
Fleur WiggenraadFrom 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 Research, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden; Ageing Epidemiology Research Unit, School of Public Health, Imperial College London, United Kingdom.
Anna Sandebring-MattonFrom 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 Research, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden; Ageing Epidemiology Research Unit, School of Public Health, Imperial College London, United Kingdom.
Alina SolomonFrom 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 Research, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden; Ageing Epidemiology Research Unit, School of Public Health, Imperial College London, United Kingdom.
Miia KivipeltoFrom 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 Research, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden; Ageing Epidemiology Research Unit, School of Public Health, Imperial College London, United Kingdom.
University of Eastern Finland · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesATN (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.

methodsWe 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).

resultsThe 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.

Indexed as

Alzheimer DiseaseAmyloidosisCognitive DysfunctionAgedAmyloid beta-PeptidesBiomarkersCross-Sectional StudiesDisease ProgressionFemaleHumansMaleMiddle AgedPeptide Fragmentstau ProteinsAmyloid beta-PeptidesBiomarkersPeptide Fragmentstau Proteins

Identifiers

PMID36130840
PMCPMC9651451
OpenAlexW4296714032

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.