Evidence map›Paper›PMID 41777515›Full record

ArticleNoro psikiyatri arsivi2026

Diagnostic Value of Serum Humanin-Like 3 Levels in Multiple Sclerosis Patients with Predominant Optic Nerve and Spinal Cord Involvement: A Preliminary Study.

Cem İsmail Küçükali, Nuray Sancar, Hande Yüceer Korkmaz, Tuncay Gündüz, Murat Kürtüncü, Erdem Tüzün

Abstract read
In one paragraph

Article in Noro psikiyatri arsivi, 2026. 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

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

1 citing paper in PubMed.

  1. 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

6 authors.

Cem İsmail KüçükaliDepartment of Neuroscience, Aziz Sancar Institute of Experimental Medicine, Institute of Graduate Studies in Health Sciences, Istanbul University, Istanbul, Türkiye.
Nuray SancarDepartment of Neuroscience, Aziz Sancar Institute of Experimental Medicine, Institute of Graduate Studies in Health Sciences, Istanbul University, Istanbul, Türkiye.
Hande Yüceer KorkmazDepartment of Neuroscience, Aziz Sancar Institute of Experimental Medicine, Institute of Graduate Studies in Health Sciences, Istanbul University, Istanbul, Türkiye.
Tuncay GündüzDepartment of Neurology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Türkiye.
Murat KürtüncüDepartment of Neurology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Türkiye.
Erdem TüzünDepartment of Neuroscience, Aziz Sancar Institute of Experimental Medicine, Institute of Graduate Studies in Health Sciences, Istanbul University, Istanbul, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Our aim was to determine whether serum levels of humanin-like 3 (encoded by the MTRNR2L3 gene) may serve as a diagnostic biomarker for differentiation of NMOSD from relapsing remitting multiple sclerosis (RRMS) presenting with clinical features reminiscent of NMOSD. Methods: Humanin-like 3 levels were measured by ELISA in sera of 30 RRMS patients, 10 NMOSD patients, 15 RRMS patients presenting predominantly with spinal cord and optic nerve attacks (MS-SCON) and 23 healthy controls. Results: MS-SCON patients showed significantly higher humanin-like 3 levels than other groups. Receiver operating characteristic (ROC) curve analysis showed that 5.26 ng/ml cut-off value of humanin-like 3 level discriminated MS-SCON from NMOSD by 66.7% sensitivity and 90% specificity. Humanin-like 3 levels did not correlate with demographic and clinical variables of MS and NMOSD. Conclusion: Serum humanin-like 3 level might potentially be used as a biomarker in differential diagnosis of MS patients presenting with NMOSD-like features. Elevated humanin-like 3 levels of MS-SCON patients might be an indicator of increased stress on neuronal survival in this MS subgroup.

Indexed as

AutoimmunityCSF-1humanin-like 3multiple sclerosismyelitis

Identifiers

PMID41777515
PMCPMC12951491

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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.