Evidence map›Paper›PMID 38213949›Full record

ArticleAlzheimer's & dementia (Amsterdam, Netherlands)

Polygenic risk for Alzheimer's disease is associated with neuroaxonal damage before onset of clinical symptoms.

Sonja M Kagerer, Swapnil Awasthi, Stephan Ripke, Aleksandra Maceski, Pascal Benkert, Aïda B Fall, Peter Riederer, Peter Fischer, Susanne Walitza, Edna Grünblatt and 2 more

Open access · goldAbstract read
In one paragraph

Article in Alzheimer's & dementia (Amsterdam, Netherlands). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. More ThanNeurology. Genetics · 2025
    Article
  3. Article
  4. Article
  5. Article
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

12 authors at 8 institutions in 6 countries.

Sonja M KagererDepartment of Geriatric Psychiatry Psychiatric University Hospital Zurich (PUK) Zurich Switzerland.
Swapnil AwasthiDepartment of Psychiatry and Psychotherapy Charité-Universitätsmedizin Berlin Germany.
Stephan RipkeDepartment of Psychiatry and Psychotherapy Charité-Universitätsmedizin Berlin Germany.
Aleksandra MaceskiDepartment of Neurology University Hospital and University of Basel Basel Switzerland.
Pascal BenkertMultiple Sclerosis Centre and Research Center for Clinical Neuroimmunology and Neuroscience (RC2NB) Departments of Biomedicine and Clinical Research University Hospital and University of Basel Basel Switzerland.
Aïda B FallGeriatric Psychiatry Service University Hospitals of Geneva (HUG) Thônex Switzerland.
Peter RiedererCenter of Mental Health Clinic and Policlinic of Psychiatry Psychosomatics and Psychotherapy University Hospital of Würzburg Würzburg Germany.
Peter FischerDepartment of Psychiatry Social Medicine Center East-Donauspital Vienna Austria.
Susanne WalitzaDepartment of Child and Adolescent Psychiatry and Psychotherapy Psychiatric University Hospital Zurich University of Zurich Zurich Switzerland.
Edna GrünblattDepartment of Child and Adolescent Psychiatry and Psychotherapy Psychiatric University Hospital Zurich University of Zurich Zurich Switzerland.
Jens KuhleDepartment of Neurology University Hospital and University of Basel Basel Switzerland.
Paul G UnschuldGeriatric Psychiatry Service University Hospitals of Geneva (HUG) Thônex Switzerland.
Charité - Universitätsmedizin Berlin · DEDepartment of Biomedicine Basel · CHUniversity Hospital of Zurich · CHUniversity of Geneva · CHDonauspital · ATSwiss Integrative Center for Human Health · CHUniversity of Basel · CHUniversity of Southern Denmark · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionEstablishing valid diagnostic strategies is a precondition for successful therapeutic intervention in Alzheimer's disease (AD).

methodsOne hundred forty-four healthy 75-year-old participants from the Vienna-Transdanube-Aging longitudinal cohort study were tested for neuroaxonal damage by single molecular array (Simoa) plasma neurofilament light chain (NfL) levels at baseline, 30, 60, and 90 months, and onset of AD dementia. Individual risk for sporadic AD was estimated by continuous shrinkage polygenic risk score (PRS-CS, genome-wide association study).

resultsNineteen participants developed AD after a median of 60 months (interquartile range 30). In participants with AD, baseline NfL plasma levels correlated with PRS-CS ( DISCUSSION: Our data suggest that polygenic risk for AD and plasma NfL closely interact years before onset of clinical symptoms. Peripheral NfL may serve as a diagnostic measure supporting early therapeutic intervention and secondary prevention in AD.

Indexed as

Alzheimer's diseasegenome‐wide association studiesneurofilament light chainplasma biomarkerpolygenic risk scoresingle molecular array

Identifiers

PMID38213949
PMCPMC10776830
OpenAlexW4390699120

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.