Evidence map›Paper›PMID 42645074›Full record

ArticleDiseases (Basel, Switzerland)2026

Phosphorylated Neurofilament Heavy Chain in Cerebrospinal Fluid and Serum as a Biomarker of Axonal Injury in Algerian Patients with Multiple Sclerosis.

Bouchra Nour El Houda Baiski, Zoulikha Mokrani, Sara Mimi Atmani, Fatma Zohra Ider, Nabila Lakri, Fatma Zohra Souid, Samia Chaib, Assia Galleze

Abstract read
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Article in Diseases (Basel, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

8 authors.

Bouchra Nour El Houda BaiskiLaboratory of Cellular and Molecular Biology, Faculty of Biological Sciences, Houari Boumediene University of Sciences and Technology (USTHB), Algiers 16111, Algeria.
Zoulikha MokraniDepartment of Biology and Organism Physiology, Faculty of Biological Sciences, Houari Boumediene University of Sciences and Technology (USTHB), Algiers 16111, Algeria.
Sara Mimi AtmaniLaboratory of Cellular and Molecular Biology, Faculty of Biological Sciences, Houari Boumediene University of Sciences and Technology (USTHB), Algiers 16111, Algeria.ORCID 0000-0001-6786-5744
Fatma Zohra IderLaboratory of Cellular and Molecular Biology, Faculty of Biological Sciences, Houari Boumediene University of Sciences and Technology (USTHB), Algiers 16111, Algeria.
Nabila LakriNeurology Department, Mohamed Seghir Nekkache Hospital, Algiers 16000, Algeria.
Fatma Zohra SouidImmunology Department, Mohamed Seghir Nekkache Hospital, Algiers 16000, Algeria.
Samia ChaibImmunology Department, Mohamed Seghir Nekkache Hospital, Algiers 16000, Algeria.
Assia GallezeLaboratory of Cellular and Molecular Biology, Faculty of Biological Sciences, Houari Boumediene University of Sciences and Technology (USTHB), Algiers 16111, Algeria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveAxonal injury is a key determinant in irreversible disability in multiple sclerosis (MS). Reliable biomarkers of neuroaxonal damage are essential for improving diagnosis, monitoring disease progression, and evaluating treatment response. This study investigated the relationship between phosphorylated neurofilament heavy chain (pNF-H), clinical characteristics, and conventional cerebrospinal fluid (CSF) and serum biomarkers in Algerian patients with MS.

methodsA total of 102 participants were enrolled. Clinical, immunological, and biochemical parameters were assessed, including the Expanded Disability Status Scale (EDSS), oligoclonal bands (OCBs), IgG index, albumin quotient, and pNF-H concentrations in paired CSF and serum samples.

resultsOCBs were detected in 85.5% of patients, and 65.21% exhibited intrathecal immunoglobulin synthesis, with a median IgG index of 0.87. Patients with progressive MS were significantly older and more disabled than those with relapsing-remitting MS (age:

conclusionsElevated pNF-H levels in CSF and serum are associated with disease severity and progressive MS, supporting their potential as complementary biomarkers of neuroaxonal damage and clinical disability in routine MS assessment.

Indexed as

axonal injurybiomarkerscerebrospinal fluidmultiple sclerosisneurodegenerationpNF-H

Identifiers

PMID42645074
PMCPMC13512889

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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.