Evidence map›Paper›PMID 41372457›Full record

ArticleScientific reports2025

A blood-based co-expression signature of LncRNAs and transcription factors in neuromyelitis optica with diagnostic and mechanistic implications.

Soudeh Ghafouri-Fard, Fatemeh Sadat Feghahati, Bashdar Mahmud Hussen, Arezou Sayad

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Article in Scientific reports, 2025. 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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5 · Who and what money

Authors and funding

4 authors.

Soudeh Ghafouri-FardDepartment of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Fatemeh Sadat FeghahatiPhytochemistry Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Bashdar Mahmud HussenDepartment of Clinical Analysis, College of Pharmacy, Hawler Medical University, Erbil, Kurdistan Region, Iraq.
Arezou SayadDepartment of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran. Ar.sayad@yahoo.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neuromyelitis optica (NMO) is an autoimmune disease that mainly affects the optic nerves and spinal cord. This disorder has been associated with dysregulation of several transcripts. We aimed to find possible peripheral markers for NMO through expression analysis of NF-κB-associated transcripts. Thus, we assessed expression of seven NF-κB-associated transcripts (including lncRNAs and mRNAs), namely ADINR, ANRIL, NKILA, PACER, DICER-AS, DILC, and CEBPA in the blood samples of NMO patients and healthy subjects. All seven transcripts demonstrated evidently higher expression in NMO patients compared with controls. The most prominent over-expression belonged to DICER-AS, followed by ADINR, PACER, NKILA, ANRIL, CEBPA, and DILC. All comparisons were statistically significant at P ≤ 0.0001, except DILC, which remained highly significant (P = 0.0001). Based on the ROC curve analyses, several transcripts, particularly, ADINR and DICER-AS could discriminate NMO patients from controls. The correlation in the expression of mentioned genes suggest a possible co-regulated lncRNA–transcription factor module in the blood of NMO patients that probably unites on NF-κB, IL-6/STAT3 and myeloid regulatory pathways. Taken together, these transcripts might be used in future biomarker discovery attempts for NMO in larger cohorts of NMO patients and controls.

Indexed as

Neuromyelitis OpticaRNA, Long NoncodingTranscription FactorsAdultBiomarkersFemaleGene Expression ProfilingGene Expression RegulationHumansMaleMiddle AgedNF-kappa BRNA, MessengerBiomarkersNF-kappa BRNA, Long NoncodingRNA, MessengerTranscription FactorsADINRANRILCEBPADICER-ASDILCNeuromyelitis opticaNF-κBNKILAPACER

Identifiers

PMID41372457
PMCPMC12816566

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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.