AI Article Synopsis

  • Long non-coding RNAs (lncRNAs) are functional transcripts linked to neurodevelopmental disorders, and this study examined their expression in the blood of epileptic patients versus normal controls.
  • Significant increases were found in two specific lncRNAs in patients, particularly highlighting a gender interaction where male patients showed higher levels compared to male controls.
  • Overall, findings suggest a potential role of these lncRNAs in epilepsy and encourage further research to explore their functions.

Article Abstract

Long non-coding RNAs (lncRNAs) are a group of functional transcripts that are not translated to proteins. Recent investigations have underscored their role in the pathogenesis of neurodevelopmental disorders. In the current investigation, we quantified expression levels of four lncRNAs (, and ) in peripheral blood of epileptic patients and normal controls. Expression of was significantly higher in patients compared with controls (Posterior beta = 1.982, = 0.001). We detected interaction effects of gender on expression of ( = 0.012). Further analyses showed over-expression of in male patients compared with male controls ( = 0.003), in spite of similar levels of expression between female cases and female controls ( = 0.77). Expression of was higher in total patients compared with total controls (Posterior beta = 1.27, = 0.02). Such difference was only observed between male patients and male controls when dividing study participants based on their gender ( = 0.012). There was no significant difference in expression of and between patients and controls. Expression levels of all lncRNAs were correlated with each other with r values ranging from 0.61 to 0.76 ( < 0.0001). However, expressions of none of lncRNAs were correlated with age of study participants. The current data implies a putative role for two lncRNAs in the pathogenesis of epilepsy and warrants future functional studies to verify the observed association.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6819822PMC
http://dx.doi.org/10.3389/fmolb.2019.00113DOI Listing

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