Evidence map›Paper›PMID 41298728›Full record

ArticleScientific reports2025

Altered expression of LINC03091 and LINC03090 LncRNAs in bipolar disorder: a case-control study.

Zeynab Ganji Zeitooni, Zeinab Shirvani-Farsani, Bahar Naghavi Gargari

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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. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Zeynab Ganji ZeitooniDepartment of Cell and Molecular Biology, Faculty of Life Sciences and Biotechnology, Shahid Beheshti University, Tehran, IR, Iran.
Zeinab Shirvani-FarsaniDepartment of Cell and Molecular Biology, Faculty of Life Sciences and Biotechnology, Shahid Beheshti University, Tehran, IR, Iran. z_shirvani@sbu.ac.ir.
Bahar Naghavi GargariDepartment of Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, IR, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long non-coding RNAs (lncRNAs) are widely expressed and play an essential role in gene regulation through various transcriptional and post-transcriptional mechanisms. Recent findings have highlighted the role of lncRNAs in sustaining cellular homeostasis and neurogenesis within the brain. An increasing number of reports have identified dysregulated lncRNAs linked to psychiatric disorders, including bipolar disorder (BD). We analyzed the expression levels of LRRC2-AS1, LINC03091, and LINC03090 lncRNAs in the blood samples of 50 patients with BD and 50 healthy individuals matched by age, sex, and ethnicity. RNA extraction and cDNA synthesis were performed, followed by real-time polymerase chain reaction to quantify lncRNA expression levels. Receiver operating characteristic (ROC) curve analysis was used to assess the biomarker potential. Furthermore, the relationship between gene expression levels and BD comorbidities was explored. Our findings revealed a significant enhancement in LINC03091 and LINC03090 expression in patients with BD compared with healthy subjects (P < 0.0001 and P = 0.02, respectively). However, the expression levels of LRRC2-AS1 was not significant (P = 0.69). ROC curve analysis indicated that LINC03091 (AUC = 0.74, P < 0.0001) and LINC03090 (AUC = 0.64, P = 0.01) expression levels could effectively differentiate patients from healthy controls. Considering these results, LINC03091 and LINC03090 may have a crucial role in BD and could serve as biomarkers for diagnostic and predictive applications.

Indexed as

Bipolar DisorderGene Expression RegulationRNA, Long NoncodingAdultBiomarkersCase-Control StudiesFemaleHumansMaleMiddle AgedROC CurveBiomarkersRNA, Long NoncodingBiomarkerBipolar disorderGene expressionLINC03090LINC03091LncRNALRRC2-AS1

Identifiers

PMID41298728
PMCPMC12657914

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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.