Evidence map›Paper›PMID 41929703›Full record

ReviewFrontiers in neuroscience2026

Neurofilament light chain but not glial fibrillary acidic protein serum levels are elevated in Wolfram syndrome.

Matthew J Jansen, Heather M Lugar, Cris M Brown, Abby F Tang, Liam J Oiknine, Ling Chen, Jonathan M Koller, Brian A Gordon, Bess A Marshall, Fumihiko Urano and 1 more

Abstract readReview
In one paragraph

Review in Frontiers in neuroscience, 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. 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

11 authors.

Matthew J Jansen *Department of Psychiatry, Washington University School of Medicine, St. Louis, MO, United States.
Heather M Lugar *Department of Psychiatry, Washington University School of Medicine, St. Louis, MO, United States.
Cris M BrownDepartment of Medicine, Washington University School of Medicine, St. Louis, MO, United States.
Abby F TangDepartment of Medicine, Washington University School of Medicine, St. Louis, MO, United States.
Liam J OiknineDepartment of Medicine, Washington University School of Medicine, St. Louis, MO, United States.
Ling ChenInstitute for Informatics, Data Science, and Biostatistics, Washington University School of Medicine, St. Louis, MO, United States.
Jonathan M KollerDepartment of Psychiatry, Washington University School of Medicine, St. Louis, MO, United States.
Brian A GordonMallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, MO, United States.
Bess A MarshallDepartment of Pediatrics, Washington University School of Medicine, St. Louis, MO, United States.
Fumihiko UranoDepartment of Medicine, Washington University School of Medicine, St. Louis, MO, United States.
Tamara HersheyDepartment of Psychiatry, Washington University School of Medicine, St. Louis, MO, United States.

Funding

WU P&FP30DK020579 · NIDDK · WASHINGTON UNIVERSITY · PI Jennifer Lynn Powers Carson · 2013 to 2026
$27.1M
Molecular Genetics of Hereditary Endoplasmic Reticulum DiabetesR01DK132090 · NIDDK · WASHINGTON UNIVERSITY · PI JANGA, SARATH CHANDRA, URANO, FUMIHIKO · 2022 to 2025
$2.2M
NIDDK NIH HHS P30 DK020579NIDDK NIH HHS R01 DK132090
6 · The paper itself

Abstract

Background: Wolfram syndrome is a rare genetic disorder caused by pathogenic variants in the Objective: To determine if serum NfL and/or GFAP levels are elevated in Wolfram syndrome compared to controls and whether they can serve as monitoring biomarkers. Methods: Serum NfL and GFAP levels were log Results: NfL levels were higher in the Wolfram group relative to all control groups ( Conclusion: Serum NfL elevation in Wolfram syndrome may reflect the ongoing, relatively slow neurodegeneration occurring in this disorder. However, without any correspondence between serum levels and currently used clinical and neuroimaging metrics, it has limited utility as a monitoring biomarker of disease progression in this patient population. Future studies may be warranted to determine if NfL could be a treatment-response marker in Wolfram syndrome clinical trials.

Indexed as

blood-based biomarkersglial fribrillary acidic protein (GFAP)neurodegenerationneurofilament light chain (NFL)neuroimagingSimoa assayWFS1Wolfram syndrome

Identifiers

PMID41929703
PMCPMC13038970

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.