Evidence map›Paper›PMID 41343058›Full record

ReviewJournal of neural transmission (Vienna, Austria : 1996)2026

Neurofilament light chain as a diagnostic and prognostic biomarker in atypical parkinsonisms: current evidence, new data, challenges, and future directions.

A Perez-Soriano, C Painous, M Fernandez, J Perez-Montesino, L de Mena, I Zaro, A Camara, Y Compta

Abstract readReview
PubMed Publisher
In one paragraph

Review in Journal of neural transmission (Vienna, Austria : 1996), 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. Trial
  2. Review
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

8 authors.

A Perez-Soriano *Parkinson's Disease & Movement Disorders Unit, Neurology Service, Hospital Clínic I Universitari de Barcelona; IDIBAPS, CIBERNED (CB06/05/0018-ISCIII), ERN- RND, Institut de Neurocicies UBNeuro (Maria de Maeztu Excellence Centre), Universitat de Barcelona, Barcelona, Catalonia, Spain.
C Painous *Parkinson's Disease & Movement Disorders Unit, Neurology Service, Hospital Clínic I Universitari de Barcelona; IDIBAPS, CIBERNED (CB06/05/0018-ISCIII), ERN- RND, Institut de Neurocicies UBNeuro (Maria de Maeztu Excellence Centre), Universitat de Barcelona, Barcelona, Catalonia, Spain.
M FernandezLab of Parkinson Disease and Other Neurodegenerative Movement Disorders: Clinical and Experimental Research, Department of Neurology, Institut D'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Hospital Clínic de Barcelona, Institut de Neurociències, Universitat de Barcelona, Barcelona, Catalonia, Spain.
J Perez-MontesinoLab of Parkinson Disease and Other Neurodegenerative Movement Disorders: Clinical and Experimental Research, Department of Neurology, Institut D'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Hospital Clínic de Barcelona, Institut de Neurociències, Universitat de Barcelona, Barcelona, Catalonia, Spain.
L de MenaLab of Parkinson Disease and Other Neurodegenerative Movement Disorders: Clinical and Experimental Research, Department of Neurology, Institut D'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Hospital Clínic de Barcelona, Institut de Neurociències, Universitat de Barcelona, Barcelona, Catalonia, Spain.
I ZaroParkinson's Disease & Movement Disorders Unit, Neurology Service, Hospital Clínic I Universitari de Barcelona; IDIBAPS, CIBERNED (CB06/05/0018-ISCIII), ERN- RND, Institut de Neurocicies UBNeuro (Maria de Maeztu Excellence Centre), Universitat de Barcelona, Barcelona, Catalonia, Spain.
A CamaraParkinson's Disease & Movement Disorders Unit, Neurology Service, Hospital Clínic I Universitari de Barcelona; IDIBAPS, CIBERNED (CB06/05/0018-ISCIII), ERN- RND, Institut de Neurocicies UBNeuro (Maria de Maeztu Excellence Centre), Universitat de Barcelona, Barcelona, Catalonia, Spain.
Y ComptaParkinson's Disease & Movement Disorders Unit, Neurology Service, Hospital Clínic I Universitari de Barcelona; IDIBAPS, CIBERNED (CB06/05/0018-ISCIII), ERN- RND, Institut de Neurocicies UBNeuro (Maria de Maeztu Excellence Centre), Universitat de Barcelona, Barcelona, Catalonia, Spain. ycompta@clinic.cat.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Atypical parkinsonian syndromes, such as multiple system atrophy (MSA) and progressive supranuclear palsy (PSP), are neurodegenerative disorders characterized by rapid progression, limited treatment options, and clinical overlap, as well as frequent misdiagnosis with Parkinson's disease (PD). Early and accurate diagnosis, together with reliable tools for prognosis, remain major unmet needs in their clinical management and for the design and interpretation of therapeutic clinical trials, particularly those aimed at disease-modification. Neurofilament light chain (NfL), a structural protein of the neuronal cytoskeleton released into cerebrospinal fluid (CSF) and blood after axonal injury, has emerged as a valuable biomarker in this context. Markedly elevated NfL levels are consistently found in MSA and PSP compared to PD, correlating with disease severity, brain atrophy, and survival. Although NfL has strong diagnostic and prognostic value at the group level, it marginally discriminates MSA from PSP as we show in this literature review and new analysis of our Barcelona cohort. Furthermore, NfL is influenced by age, comorbidities, and analytical variability. The correlation between its levels in CSF and blood, while consistently replicated, remains moderate, and their associations with clinical outcomes and disease progression are yet to be fully defined. This review summarizes current evidence on the role of NfL in MSA and PSP, covering its applications in diagnosis, prognosis, clinical trials, and real-world practice, as well as outlining the main challenges and future directions for its broader clinical translation.

Indexed as

Multiple System AtrophyNeurofilament ProteinsSupranuclear Palsy, ProgressiveBiomarkersHumansPrognosisBiomarkersneurofilament protein LNeurofilament ProteinsAtypical parkinsonismsBiomarkerBloodCerebrospinal fluid (CSF)Corticobasal degeneration (CBD)ELISAMultiple system atrophy (MSA)Neurofilament light chain (NfL)Progressive supranuclear palsy (PSP)Simoa

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.