Evidence map›Paper›PMID 26263977›Full record

ReviewInternational journal of molecular sciences2015

Brain-Specific Cytoskeletal Damage Markers in Cerebrospinal Fluid: Is There a Common Pattern between Amyotrophic Lateral Sclerosis and Primary Progressive Multiple Sclerosis?

Ahmed Abdelhak, Andreas Junker, Johannes Brettschneider, Jan Kassubek, Albert C Ludolph, Markus Otto, Hayrettin Tumani

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 10% of its field
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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Multiple Sclerosis: Pathogenesis Mechanism and Biomarkers.Central nervous system agents in medicinal chemistry · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Significance of CSF NfL and tau in ALS.Journal of neurology · 2018
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. 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

7 authors at 2 institutions in 1 country.

Ahmed AbdelhakDepartment of Neurology, Ulm University, Oberer Eselsberg 45, 89081 Ulm, Germany. ahmed.abdelhak@uni-ulm.de.
Andreas JunkerInstitute of Neuropathology, University Hospital Göttingen, Robert-Koch-Str 40, 37075 Göttingen, Germany. andreas.junker@med.uni-goettingen.de.
Johannes BrettschneiderDepartment of Neurology, Ulm University, Oberer Eselsberg 45, 89081 Ulm, Germany. jbre@mail.med.upenn.edu.
Jan KassubekDepartment of Neurology, Ulm University, Oberer Eselsberg 45, 89081 Ulm, Germany. jan.kassubek@uni-ulm.de.
Albert C LudolphDepartment of Neurology, Ulm University, Oberer Eselsberg 45, 89081 Ulm, Germany. albert.ludolph@rku.de.
Markus OttoDepartment of Neurology, Ulm University, Oberer Eselsberg 45, 89081 Ulm, Germany. markus.otto@uni-ulm.de.
Hayrettin TumaniDepartment of Neurology, Ulm University, Oberer Eselsberg 45, 89081 Ulm, Germany. hayrettin.tumani@uni-ulm.de.
Universität Ulm · DEUniversity of Göttingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many neurodegenerative disorders share a common pathophysiological pathway involving axonal degeneration despite different etiological triggers. Analysis of cytoskeletal markers such as neurofilaments, protein tau and tubulin in cerebrospinal fluid (CSF) may be a useful approach to detect the process of axonal damage and its severity during disease course. In this article, we review the published literature regarding brain-specific CSF markers for cytoskeletal damage in primary progressive multiple sclerosis and amyotrophic lateral sclerosis in order to evaluate their utility as a biomarker for disease progression in conjunction with imaging and histological markers which might also be useful in other neurodegenerative diseases associated with affection of the upper motor neurons. A long-term benefit of such an approach could be facilitating early diagnostic and prognostic tools and assessment of treatment efficacy of disease modifying drugs.

Indexed as

Amyotrophic Lateral SclerosisBiomarkersBrainBrain InjuriesCytoskeletonHumansMotor NeuronsMultiple Sclerosis, Chronic Progressivetau ProteinsTubulinBiomarkerstau ProteinsTubulinamyotrophic lateral sclerosis (ALS)biomarkerneurofilamentsprimary progressive multiple sclerosis (PPMS)tautubulin

Identifiers

PMID26263977
PMCPMC4581209
OpenAlexW1933799322

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.