Evidence map›Paper›PMID 40988568›Full record

Observational studyBrain : a journal of neurology2026

Neurofilament light chain as a prognostic marker in cerebral adrenoleukodystrophy.

Elizabeth I Pierpont, Ashish O Gupta, Julie B Eisengart, Ryan Shanley, Rhys O Evans, Daniel J Loes, David Nascene, Srikala Narayanan, Paul J Orchard, Troy C Lund

Abstract readObservational Study
In one paragraph

Observational study in Brain : a journal of neurology, 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

10 authors.

Elizabeth I PierpontDepartment of Pediatrics, University of Minnesota, Masonic Institute for the Developing Brain, Minneapolis, MN 55414, USA.ORCID 0000-0001-7555-8613
Ashish O GuptaDepartment of Pediatrics, University of Minnesota, Masonic Cancer Center, Minneapolis, MN 55455, USA.ORCID 0000-0001-5679-5533
Julie B EisengartDepartment of Pediatrics, University of Minnesota, Masonic Institute for the Developing Brain, Minneapolis, MN 55414, USA.ORCID 0000-0001-5340-017X
Ryan ShanleyBiostatistics and Bioinformatics Core, University of Minnesota, Masonic Cancer Center, Minneapolis, MN 55455, USA.
Rhys O EvansDepartment of Pediatrics, University of Minnesota, Masonic Institute for the Developing Brain, Minneapolis, MN 55414, USA.
Daniel J LoesDepartment of Radiology, University of Minnesota Medical School, Minneapolis, MN 55455, USA.
David NasceneDepartment of Radiology, University of Minnesota Medical School, Minneapolis, MN 55455, USA.
Srikala NarayananDepartment of Radiology, Texas Children's Hospital, Baylor College of Medicine, Houston TX 77030, USA.
Paul J OrchardDepartment of Pediatrics, University of Minnesota, Masonic Cancer Center, Minneapolis, MN 55455, USA.
Troy C LundDepartment of Pediatrics, University of Minnesota, Masonic Cancer Center, Minneapolis, MN 55455, USA.ORCID 0000-0001-9174-8919

Funding

University of Minnesota Clinical and Translational Science Institute (UMN CTSI)UM1TR004405 · NCATS · UNIVERSITY OF MINNESOTA · PI Bruce R Blazar, Damien A Fair · 2023 to 2026
$30.8M
Neurocognitive and neuroimaging markers of emerging cerebral adrenoleukodystrophyK23NS123258 · NINDS · UNIVERSITY OF MINNESOTA · PI Elizabeth Irene Pierpont · 2022 to 2026
$794k
NCATS NIH HHS K23NS123258NCATS NIH HHS UM1TR004405NINDS NIH HHS K23 NS123258the University of Minnesota Foundation
6 · The paper itself

Abstract

Cerebral adrenoleukodystrophy (C-ALD) is a rapidly progressing inflammatory neurodegenerative disease with unpredictable onset in males with ALD. It must be treated at an early stage of demyelination, determined by MRI, to preserve neurocognitive function. Validation of biochemical markers that can aid in the prediction of functional outcomes is needed for optimizing disease management and therapeutic development. Our objective was to determine whether plasma neurofilament light chain (NfL), a biomarker of neuroaxonal injury, corresponds to functional outcomes after standard of care treatment with haematopoietic stem cell transplantation (HSCT). This retrospective observational cohort study of 27 patients with C-ALD treated with HSCT at a mean age of 8.0 years (standard deviation = 2.6) examined pre-treatment biomarker levels and neurocognitive outcomes 1 year after treatment. Plasma biospecimens were collected at a median of 10 days prior to HSCT, and NfL concentrations were measured with Single-Molecule Array (SiMoA) assay. White matter lesions were characterized by Loes MRI severity scores. Following treatment, neurocognitive outcomes across six domains were measured at a median of 1 year post-HSCT using the Wechsler intelligence quotient (IQ) scales, the Beery-Buktenica Test of Visual-Motor Integration and the Purdue Pegboard test. Pre-HSCT NfL values in C-ALD patients ranged from 5.0 to 911.0 pg/ml, with a median of 35.8 pg/ml. Higher NfL levels were associated with lower post-HSCT scores across all neurocognitive domains (P < 0.05). Large effect sizes were seen for visual reasoning, processing speed, fine motor dexterity and visual-motor integration (Pearson correlations: r = -0.74 to -0.84). Partial correlations showed a moderate association between NfL and neurocognitive outcomes, even when adjusting for MRI severity scores. NfL has a strong correlation with neurocognitive status following treatment for C-ALD. These encouraging findings suggest an opportunity to improve our capacity to forecast outcomes and therefore improve counselling for families considering cellular therapies.

Indexed as

AdrenoleukodystrophyNeurofilament ProteinsAdolescentBiomarkersChildChild, PreschoolCohort StudiesFemaleHematopoietic Stem Cell TransplantationHumansMagnetic Resonance ImagingMalePrognosisRetrospective StudiesBiomarkersneurofilament protein LNeurofilament ProteinsABCD1bloodclinical outcome assessmentsneuropsychologyperoxisomalX-linked

Identifiers

PMID40988568
PMCPMC13017199

What OpenQuestion holds

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LicenceCC BY-NC
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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.