Author/Authors :
Shafiei, Jalil Department of Genetic - Science and Research Branch Islamic Azad University, Tehran, Iran , Javadi, Gholamreza Department of Genetic - Science and Research Branch Islamic Azad University, Tehran, Iran , Nateghi, Behnaz Department of Biochemistry - Faculty of Science - Nourdanesh Institutions of Higher Education, Meimeh, Isfahan, Iran , Shaygannejad, Vahid Department of Neurology - Isfahan Neurosciences Research Center - Isfahan University of Medical Sciences, Isfahan, Iran , Salehi, Mansoor Department of Genetics and Molecular Biology - School of Medicine - Isfahan University of Medical Sciences, Isfahan, Iran
Abstract :
Introduction: Multiple sclerosis (MS) is an inflammatory demyelinating in which there is no
standardized method to detect this disease activity. It has shown abnormal microRNAs (miRNAs)
function in peripheral blood immune cells. miRNAs expression is probably responsible for
immunological features associated with MS. The purpose of the current study was to investigate the
association of miR-93-5p expression with MS disease.
Materials and methods: In this case-control study, a totally of 30 relapsing-remitting MS (RRMS)
patients and 30 healthy subjects were enrolled. Following miRNA extraction and cDNA synthesis, miR-
93-5p expression was examined in peripheral blood mononuclear cells (PBMCs) using real-time
polymerase chain reaction.
Results: The expression of miR-93-5p was significantly increased in RRMS patients compared to
healthy subjects (P=0.001). Receiver operating curve (ROC) analysis identified a strong predictive
power of miR‑93-5p on discriminating MS from healthy individuals, with the area under the curve
(AUC) of 0.939 (95% CI; 0.8581-1.000). On the other hand, the samples were analyzed based on the
type of drug treatment (interferon and non-interferon), which did not show any considerable differences
(P=0.863).
Conclusion: Our findings showed that miR-93-5p has highly elevated expression in patients with
RRMS compared to healthy subjects. Based on the results miR-93-5p may be a prospective biomarker
with the potential use for diagnosis of RRMS patients.