Evidence map›Paper›PMID 42649149›Full record

ArticleTranslational psychiatry2026

Exploring serum biomarkers in paediatric psychiatry: the impact of NfL and GFAP.

Marc Pawlitzki, Lars Masanneck, Laura Schlarbaum, Nicole Jankovic, Stefan Bittner, Falk Steffen, Jens Kuhle, Pascal Benkert, Jonathan Repple, Judith Bühlmeier and 6 more

Abstract read
In one paragraph

Article in Translational psychiatry, 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

16 authors.

Marc Pawlitzki *Department of Neurology, Medical Faculty University Hospital Düsseldorf, Düsseldorf, Germany. marcguenter.pawlitzki@med.uni-duesseldorf.de.ORCID http://orcid.org/0000-0003-3080-2277
Lars Masanneck *Department of Neurology, Medical Faculty University Hospital Düsseldorf, Düsseldorf, Germany.ORCID http://orcid.org/0000-0003-2496-1415
Laura SchlarbaumPaderborn University, Faculty of Natural Sciences, Institute of Nutrition, Consumption and Health, Paderborn, Germany.ORCID http://orcid.org/0009-0001-4969-4459
Nicole JankovicPaderborn University, Faculty of Natural Sciences, Institute of Nutrition, Consumption and Health, Paderborn, Germany.
Stefan BittnerDepartment of Neurology, Focus Program Translational Neuroscience (FTN) and Immunotherapy (FZI), Rhine Main Neuroscience Network (RMN2), Medical Center, Johannes Gutenberg University Mainz, Mainz, Germany.
Falk SteffenDepartment of Neurology, Focus Program Translational Neuroscience (FTN) and Immunotherapy (FZI), Rhine Main Neuroscience Network (RMN2), Medical Center, Johannes Gutenberg University Mainz, Mainz, Germany.ORCID http://orcid.org/0000-0003-3708-8600
Jens KuhleMultiple 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.ORCID http://orcid.org/0000-0002-6963-8892
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.
Jonathan ReppleGoethe University Frankfurt, University Hospital, Department of Psychiatry, Psychosomatic Medicine and Psychotherapy, Frankfurt, Germany.ORCID http://orcid.org/0000-0003-1379-9491
Judith BühlmeierPaderborn University, Faculty of Natural Sciences, Institute of Nutrition, Consumption and Health, Paderborn, Germany.
Anke HinneyCenter for Translational Neuro- and Behavioral Sciences, University Hospital Essen, Essen, Germany.ORCID http://orcid.org/0000-0001-5659-0706
Johannes HebebrandDepartment of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
Raphael HirtzHelios University Medical Centre Wuppertal - Children's Hospital, Witten/Herdecke University, Wuppertal, Germany.
Sven G MeuthDepartment of Neurology, Medical Faculty University Hospital Düsseldorf, Düsseldorf, Germany.
Lars Libuda *Paderborn University, Faculty of Natural Sciences, Institute of Nutrition, Consumption and Health, Paderborn, Germany.
Manuel Föcker *Department of Child and Adolescent Psychiatry, University Hospital Münster, Münster, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Serum neurofilament light chain (sNfL) and glial fibrillary acidic protein (GFAP) are biomarkers of neuroaxonal and astrocytic damage but remain understudied in adolescent psychiatric populations. This study investigated sNfL and GFAP levels in 412 adolescents diagnosed with anorexia nervosa (AN) (n = 52), depression (n = 237), and other psychiatric disorders (n = 123). We assessed their diagnostic utility, correlation with disease severity, and longitudinal changes during AN treatment. Biomarkers were measured using Single Molecule Array technology, with Z-scores derived from reference datasets. Compared to population norms, both biomarkers were elevated in AN (sNfL: 1.15 ± 1.17; GFAP: 1.50 ± 0.84) and in depression (sNfL: 0.34 ± 1.10; GFAP: 0.58 ± 1.00). Patients with AN showed significantly higher biomarker levels than those with depression or other psychiatric disorders; importantly, this distinction remained evident in sensitivity analyses restricted to underweight individuals with depression. In AN, sNfL levels correlated with baseline weight loss (β = -0.45, R² = 0.20) and declined significantly during treatment, while GFAP changes were less pronounced. Neither marker correlated with depressive symptom severity. Bootstrapped ROC analyses showed moderate-to-good discriminatory power (AUCs 0.70-0.84) for distinguishing AN from depression. These findings suggest that neuroaxonal and astrocytic stress is a component of adolescent psychopathology, particularly in AN. sNfL appears sensitive to starvation-related neurobiological changes, with levels normalizing alongside weight restoration. GFAP showed similar but less robust trends. Accordingly, the observed biomarker changes reflect more than underweight alone, supporting a potential role in differential diagnosis and treatment monitoring.

Indexed as

Anorexia NervosaDepressive DisorderGlial Fibrillary Acidic ProteinMental DisordersNeurofilament ProteinsAdolescentBiomarkersChildFemaleHumansMaleSeverity of Illness IndexBiomarkersGFAP protein, humanGlial Fibrillary Acidic Proteinneurofilament protein LNeurofilament Proteins

Identifiers

PMID42649149
PMCPMC13518902

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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.