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Peripheral expression of long non-coding RNAs in bipolar patients
Arezou Sayad1, Mohammad Taheri2, Mir Davood Omrani3
1Department of Medical Genetics, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Journal of Affective Disorders
|February 18, 2019
Summary
Certain long non-coding RNAs (lncRNAs) show altered expression in bipolar disorder (BD). Specific lncRNAs like TUG1 demonstrate high diagnostic power for BD, suggesting their potential as biomarkers.
Area of Science:
- Molecular Biology
- Genetics
- Neuroscience
Background:
- Long non-coding RNAs (lncRNAs) are implicated in the pathogenesis of various human disorders, including neuropsychiatric conditions.
- Understanding the role of specific lncRNAs in bipolar disorder (BD) is crucial for advancing diagnostic and therapeutic strategies.
Purpose of the Study:
- To investigate the expression levels of six apoptosis-related lncRNAs (CCAT2, TUG1, PANDA, NEAT1, FAS-AS1, and OIP5-AS1) in bipolar disorder patients.
- To assess the potential contribution of these lncRNAs to the pathogenesis of BD.
- To evaluate the diagnostic utility of these lncRNAs as biomarkers for BD.
Main Methods:
- Expression profiling of six apoptosis-related lncRNAs in peripheral blood samples from BD patients and healthy controls.
- Statistical analysis to compare lncRNA expression between groups and identify significant differences.
- Receiver operating characteristic (ROC) curve analysis to determine the diagnostic power of individual lncRNAs and their combinations.
Main Results:
- CCAT2, TUG1, and PANDA were significantly upregulated, while OIP5-AS1 was downregulated in BD patients compared to healthy controls.
- Sex-specific differences in lncRNA expression were observed, with CCAT2 and TUG1 differing in males, and PANDA in both males and females.
- TUG1 exhibited the highest diagnostic power individually, and a combination of CCAT2, TUG1, PANDA, and OIP5-AS1 achieved a diagnostic power of 0.96, indicating high sensitivity and specificity.
Conclusions:
- Specific lncRNAs, including CCAT2, TUG1, PANDA, and OIP5-AS1, play a potential role in the pathogenesis of bipolar disorder.
- These lncRNAs demonstrate significant potential as diagnostic biomarkers for bipolar disorder, warranting further investigation.
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