Evidence map›Paper›PMID 42137304›Full record

ArticleResearch (Washington, D.C.)2026

Artificial Intelligence Decodes Brain Elemental Signatures to Stratify Aging and Neurological Diseases.

Augustin Tillement, Eszter Nemeth, Laurent David, Dilek Cenesiz, Ulrich Neumayer, Mathias Fousse, Yang Liu, Walter J Schulz-Schaeffer, Klaus Fassbender, Alexandre Detappe and 4 more

Abstract read
In one paragraph

Article in Research (Washington, D.C.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Augustin TillementIngénierie des Matériaux Polymères (IMP), UMR 5223, Universite Claude Bernard Lyon 1, INSA de Lyon, Université Jean Monnet, CNRS, F-69622 Villeurbanne, France.
Eszter NemethDepartment of Neurology, Saarland University Medical Center, D-66421 Homburg, Germany.
Laurent DavidIngénierie des Matériaux Polymères (IMP), UMR 5223, Universite Claude Bernard Lyon 1, INSA de Lyon, Université Jean Monnet, CNRS, F-69622 Villeurbanne, France.
Dilek CenesizDepartment of Neurology, SHG Klinikum Merzig, D-66663 Merzig, Germany.
Ulrich NeumayerDepartment of Neurology, SHG Klinikum Merzig, D-66663 Merzig, Germany.
Mathias FousseDepartment of Neurology, Saarland University Medical Center, D-66421 Homburg, Germany.
Yang LiuDepartment of Neurology, Saarland University Medical Center, D-66421 Homburg, Germany.
Walter J Schulz-SchaefferInstitute of Neuropathology, Medical Faculty of the Saarland University, D-66421 Homburg, Germany.
Klaus FassbenderDepartment of Neurology, Saarland University Medical Center, D-66421 Homburg, Germany.
Alexandre DetappeNanomedicine Laboratory, Institut de Cancérologie Strasbourg Europe, F-67000 Strasbourg, France.
François LuxInstitut Lumière Matière (ILM), UMR5306, Universite Claude Bernard Lyon 1, CNRS, F-69100 Villeurbanne, France.
Sergiu GroppaDepartment of Neurology, Saarland University Medical Center, D-66421 Homburg, Germany.
Olivier TillementInstitut Lumière Matière (ILM), UMR5306, Universite Claude Bernard Lyon 1, CNRS, F-69100 Villeurbanne, France.
Yann DeckerDepartment of Neurology, Saarland University Medical Center, D-66421 Homburg, Germany.ORCID https://orcid.org/0000-0002-9426-9355

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The elemental composition of brains changes progressively with age, yet these metallome alterations remain largely unexplored as diagnostic biomarkers in neurological disease. Here, we present a comprehensive analysis of 24 inorganic elements in paired cerebrospinal fluid and serum samples from 1,608 individuals spanning healthy aging through 14 neurological conditions, representing the largest systematically standardized cohort for neurological metallomics. Uniquely, our unselected, consecutively admitted clinical cohort captures the full heterogeneity of neurological presentations, overcoming the limitations of traditional case-control designs focused on isolated disease entities. Machine learning analysis reveals that aging is associated with distinct cerebrospinal fluid elemental signatures independent of peripheral blood changes, primarily reflecting blood-brain barrier permeability alterations that correlate with established albumin quotient measurements. We identify 2 predominant patterns of neurological elemental dysregulation: one mainly consistent with passive barrier-mediated leakage in inflammatory conditions, and another mainly indicative of disease-intrinsic perturbations of metal homeostasis in neurodegenerative disorders. Age-stratified analysis reveals that elemental signatures evolve differently across the lifespan for distinct pathological processes. The integration of elemental signatures with routine clinical parameters through ensemble learning approaches enhances diagnostic accuracy across all tested neurological categories, establishing metallomics as a complementary biomarker class that captures orthogonal pathophysiological information. These findings establish brain metallomics as an emerging field where artificial intelligence reveals complex multi-element interactions present in neurological aging, opening new avenues for precision medicine in age-related neurological disorders.

Identifiers

PMID42137304
PMCPMC13168758

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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.