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.
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.
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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.
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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- The MTRNR2L gene family and age-related macular degeneration.Frontiers in immunology · 2026Review
Corrections and comments
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
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.
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Registered trials
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