Evidence map›Paper›PMID 41917159›Full record

ArticleNature medicine2026

A deep joint-learning proteomics model for diagnosis of six conditions associated with dementia.

Lijun An, Alexa Pichet Binette, Ines Hristovska, Gabriele Vilkaite, Yu Xiao, Romina Zendehdel, Zijian Dong, Bart Smets, Rowan Saloner, Shinya Tasaki and 13 more

Abstract read
In one paragraph

Article in Nature medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–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

2 citing papers in PubMed.

  1. Article
  2. Engineering in vivo CAR-T cells.Nature medicine · 2026
    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

23 authors.

Lijun AnDepartment of Clinical Sciences Malmö, SciLifeLab, Lund University, Lund, Sweden. lijun.an@med.lu.se.ORCID http://orcid.org/0000-0003-1030-4625
Alexa Pichet BinetteClinical Memory Research Unit, Department of Clinical Sciences Malmö, Lund University, Lund, Sweden.
Ines HristovskaClinical Memory Research Unit, Department of Clinical Sciences Malmö, Lund University, Lund, Sweden.
Gabriele VilkaiteDepartment of Clinical Sciences Malmö, SciLifeLab, Lund University, Lund, Sweden.ORCID http://orcid.org/0009-0009-6985-4307
Yu XiaoDepartment of Clinical Sciences Malmö, SciLifeLab, Lund University, Lund, Sweden.
Romina ZendehdelDepartment of Clinical Sciences Malmö, SciLifeLab, Lund University, Lund, Sweden.
Zijian DongCentre for Sleep and Cognition and Centre for Translational MR Research, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Bart SmetsJohnson & Johnson, Beerse, Belgium.
Rowan SalonerMemory and Aging Center, Department of Neurology, Weill Institute for Neurosciences, University of California, San Francisco, CA, USA.ORCID http://orcid.org/0000-0002-1351-6183
Shinya TasakiRush Alzheimer's Disease Center, Rush University Medical Center, Chicago, IL, USA.ORCID http://orcid.org/0000-0003-3656-7394
Ying XuDepartment of Psychiatry, Washington University School of Medicine, St. Louis, MO, USA.ORCID http://orcid.org/0009-0006-0387-2439
Varsha KrishGates Ventures, Seattle, WA, USA.
Farhad ImamGates Ventures, Seattle, WA, USA.ORCID http://orcid.org/0000-0003-2854-2568
Shorena JanelidzeClinical Memory Research Unit, Department of Clinical Sciences Malmö, Lund University, Lund, Sweden.ORCID http://orcid.org/0000-0003-2869-8378
Danielle van WestenDepartment of Diagnostic Radiology, Clinical Sciences, Lund University, Lund, Sweden.ORCID http://orcid.org/0000-0001-8649-9874
Global Neurodegenerative Proteomics Consortium (GNPC)
Erik StomrudClinical Memory Research Unit, Department of Clinical Sciences Malmö, Lund University, Lund, Sweden.
Christopher D WhelanRCSI University of Medicine and Health Sciences, Royal College of Surgeons in Ireland, Dublin, Ireland.
Sebastian PalmqvistClinical Memory Research Unit, Department of Clinical Sciences Malmö, Lund University, Lund, Sweden.ORCID http://orcid.org/0000-0002-9267-1930
Rik OssenkoppeleClinical Memory Research Unit, Department of Clinical Sciences Malmö, Lund University, Lund, Sweden.
Niklas Mattsson-CarlgrenClinical Memory Research Unit, Department of Clinical Sciences Malmö, Lund University, Lund, Sweden.ORCID http://orcid.org/0000-0002-8885-7724
Oskar HanssonClinical Memory Research Unit, Department of Clinical Sciences Malmö, Lund University, Lund, Sweden.ORCID http://orcid.org/0000-0001-8467-7286
Jacob W VogelDepartment of Clinical Sciences Malmö, SciLifeLab, Lund University, Lund, Sweden. jacob.vogel@med.lu.se.ORCID http://orcid.org/0000-0001-6394-9940

Funding

Crafoordska Stiftelsen (Crafoord Foundation) 20230790Knut och Alice Wallenbergs Stiftelse (Knut and Alice Wallenberg Foundation) KAW 2020.0239U.S. Department of Health & Human Services | NIH | National Institute on Aging (U.S. National Institute on Aging) U01 AG079847-02Vetenskapsrådet (Swedish Research Council) 2024-03642
6 · The paper itself

Abstract

Co-pathology is a common feature of neurodegenerative diseases that complicates diagnosis, treatment and clinical management. However, sensitive, specific and scalable biomarkers for in vivo pathological diagnosis are not available for most neurodegenerative neuropathologies. Here we present Proteomics-based Artificial Intelligence for Dementia Diagnosis (ProtAIDe-Dx), a deep joint-learning model on 17,187 patients and controls (age of 70.3 ± 11.5 years, 53.2% female), that uses plasma proteomics to provide simultaneous probabilistic diagnosis across 6 conditions associated with dementia in aging. ProtAIDe-Dx achieves cross-validated balanced classification accuracy of 70-95% and area under the curve of >78% across all conditions. The model's diagnostic probabilities highlighted subgroups of patients with co-pathologies and were associated with pathology-specific biomarkers in an external memory clinic sample, even among individuals without cognitive impairment. Model interpretation revealed a suite of protein networks marking shared and specific biological processes across diseases and identified novel and previously described proteins discriminating each diagnosis. ProtAIDe-Dx significantly improved biomarker-based differential diagnosis in a memory clinic sample, pinpointing proteins leading to diagnostic decisions at an individual level. Together, this work highlights the promise of plasma proteomics to improve patient-level diagnostic workup with a single blood draw.

Indexed as

Deep LearningDementiaProteomicsAgedAlzheimer DiseaseBiomarkersFemaleHumansMaleMiddle AgedBiomarkers

Identifiers

PMID41917159
PMCPMC13190262

What OpenQuestion holds

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Registered trials

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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.