Evidence map›Paper›PMID 39891767›Full record

ArticleJournal of neurology2025

Serum neurofilament light chain but not serum glial fibrillary acidic protein is a marker of early Huntington's disease.

Beatrice Heim, Elias Mandler, Marina Peball, Federico Carbone, Katarína Schwarzová, Rina Demjaha, Cansu Tafrali, Arabella Buchmann, Michael Khalil, Atbin Djamshidian and 1 more

Abstract read
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Article in Journal of neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

11 authors.

Beatrice HeimDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria. Beatrice.heim@i-med.ac.at.ORCID http://orcid.org/0000-0002-6749-3044
Elias MandlerDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Marina PeballDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Federico CarboneDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Katarína SchwarzováDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Rina DemjahaDepartment of Neurology, Medical University of Graz, Graz, Austria.
Cansu TafraliDepartment of Neurology, Medical University of Graz, Graz, Austria.
Arabella BuchmannDepartment of Neurology, Medical University of Graz, Graz, Austria.
Michael KhalilDepartment of Neurology, Medical University of Graz, Graz, Austria.
Atbin DjamshidianDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Klaus SeppiDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria. klaus.seppi@i-med.ac.at.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHuntington's disease (HD) is caused by CAG trinucleotide expansion on chromosome 4, leading to mutant Huntingtin production. Premanifest carriers show no obvious clinical signs, and early symptoms progress slowly. Fluid biomarkers like neurofilament light (NfL) and glial fibrillary acidic protein (GFAP), measurable in cerebrospinal fluid and serum (sNfL, sGFAP), offer potential predicting HD progression.

objectiveTo assess the role of sGFAP and sNfL and clinical biomarkers in different disease stages and correlate with disease progression.

methodsHD mutation carriers were categorized into clinical stages according to their motor symptoms and functional capacities. The Unified HD Rating Scale, cognitive assessments and olfactory tests were used to characterize the patients clinically. Furthermore, sNfL and sGFAP levels were assessed.

resultsWe consecutively included 44 HD mutation carriers (13 premanifest HD (preHD), 18 in early (early HD) and 13 in advanced (advanced HD) disease stages) and 19 healthy controls (HC). Advanced HD patients performed worse on all clinical tasks and had higher sGFAP and sNfL levels compared to other groups (all p values < 0.05). We did not find difference in sGFAP levels between the preHD, early HD and HC group  (all p values > 0.05). In contrast, sNfL levels differed significantly between preHD and early HD, and HC (all p values < 0.05). ROC curve analysis revealed that the AUC of sGFAP (0.970) exhibited superior discriminatory accuracy compared to sNfL (0.791) levels in separating advanced from early HD patients. By contrast, ROC curve analysis revealed that the AUC of sNFL (0.988) exhibited superior discriminatory accuracy compared to sGFAP (0.609) levels in separating all HD mutation carriers from HC.

conclusionsOur study indicates that sNfL can detect changes in very early and premanifest HD stages, whereas sGFAP showed differences in more advanced stages only.

Indexed as

Glial Fibrillary Acidic ProteinHuntington DiseaseNeurofilament ProteinsAdultBiomarkersDisease ProgressionFemaleHumansMaleMiddle AgedROC CurveSeverity of Illness IndexBiomarkersGFAP protein, humanGlial Fibrillary Acidic Proteinneurofilament protein LNeurofilament ProteinsBiomarkersGlial fibrillary acidic proteinHuntington’s diseaseMutation carriersNeurocognitionNeurofilament lightOlfactory dysfunction

Identifiers

PMID39891767
PMCPMC11787204

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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.