Evidence map›Paper›PMID 41326959›Full record

ArticleAlzheimer's & dementia : the journal of the Alzheimer's Association2025

Enhancing diagnostic precision in Alzheimer's disease: Impact of comorbidities on blood biomarkers for clinical integration.

Makrina Daniilidou, Ulf Öhlund-Wistbacka, Göran Hagman, Anna Rosenberg, Nicholas Ashton, Henrik Zetterberg, Kaj Blennow, Anna Matton, Miia Kivipelto

Abstract read
In one paragraph

Article in Alzheimer's & dementia : the journal of the Alzheimer's Association, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Diagnostic accuracy of plasma p-tau217 against amyloid PET: A meta-analysis of technical platform variability and ratio versus single marker comparisons.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
    Pooled it
  2. Article
  3. Review
  4. Reliable quantification of renal function from frozen blood samples.medRxiv : the preprint server for health sciences · 2026
    Article
  5. Article
  6. Article
  7. 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

9 authors.

Makrina DaniilidouDivision of Clinical Geriatrics, Centre for Alzheimer Research, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Solna, Sweden.ORCID 0000-0002-5460-9802
Ulf Öhlund-WistbackaDivision of Clinical Geriatrics, Centre for Alzheimer Research, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Solna, Sweden.
Göran HagmanDivision of Clinical Geriatrics, Centre for Alzheimer Research, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Solna, Sweden.
Anna RosenbergDivision of Clinical Geriatrics, Centre for Alzheimer Research, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Solna, Sweden.
Nicholas AshtonDepartment of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, the Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden.
Henrik ZetterbergDepartment of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, the Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden.
Kaj BlennowDepartment of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, the Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden.
Anna MattonDivision of Clinical Geriatrics, Centre for Alzheimer Research, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Solna, Sweden.
Miia KivipeltoDivision of Clinical Geriatrics, Centre for Alzheimer Research, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Solna, Sweden.

Funding

AlzheimerfondenAlzheimer's Drug Discovery FoundationCenter for Innovative MedicineGun och Bertil Stohnes StiftelseInnovative Health Initiative Joint Undertaking (IHI JU)- AD-RIDDLE 101132933Innovative Health Initiative Joint Undertaking (IHI JU) -PROMINENT 101112145Karolinska Institutet fund for Geriatric Research (SE)Region Stockholm research grant-ALF, SwedenStiftelsen för Gamla TjänarinnorStiftelsen Stockholms sjukhem (SE)Swedish research council for health, working life and welfare (FORTE)
6 · The paper itself

Abstract

introductionComorbidities may influence Alzheimer's disease (AD) plasma biomarkers. This study aimed to investigate how medical conditions impact AD plasma biomarkers and whether comorbidity-adjusted models enhance their diagnostic performance.

methodsWe analyzed key AD plasma biomarkers in 311 memory clinic patients (mean age 59 years, 57% female) at Karolinska University Hospital, Sweden. Biomarkers were measured using single molecular array (SIMOA) and Lumipulse assay. Multivariate linear regressions and receiver operating characteristic/area under the curves (ROC/AUCs) were calculated using clinical diagnosis and cerebrospinal fluid biomarkers as gold standards.

resultsPlasma biomarkers were associated with comorbidities and metabolites such as estimated glomerular filtration rate, homocysteine, and high-density lipoprotein. Phosphorylated tau (p-tau)/amyloid beta (Aβ)42 and p-tau217 had excellent performances in AD pathology classification (AUCs > 0.938). Adjusting for comorbidity measures significantly improved the diagnostic accuracy of Aβ42/40. DISCUSSION: In conclusion, plasma biomarkers performed robustly despite comorbidity associations, with p-tau217 emerging as the strongest discriminator. These findings support their potential as diagnostic tools in clinical settings. HIGHLIGHTS: Plasma biomarkers for Alzheimer's disease (AD) were assessed in a real-world memory clinic population. Kidney dysfunction and cardiovascular risk factors influenced plasma biomarker levels. Phosphorylated tau (p-tau)217 and p-tau217/amyloid beta (Aβ)42 ratio showed strongest association with AD pathology. Aβ42/40 ratio's accuracy was improved by including comorbidities into the diagnostic algorithms.

Indexed as

Alzheimer DiseaseAmyloid beta-PeptidesBiomarkerstau ProteinsAgedComorbidityFemaleHumansMaleMiddle AgedPeptide FragmentsSwedenAmyloid beta-PeptidesBiomarkersPeptide Fragmentstau ProteinsAlzheimer's diseaseamyloid beta 42/40 ratioblood biomarkerscomorbiditiesdiagnostic accuracyphosphorylated tau217

Identifiers

PMID41326959
PMCPMC12668905

What OpenQuestion holds

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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.