El Samaloty Nourhan M, Hassan Zeinab A, Hefny Zeinab M, Abdelaziz Dalia H A
Department of Biochemistry and Molecular Biology, Faculty of Pharmacy, Future University, Egypt.
Department of Biochemistry and Molecular Biology, Faculty of Pharmacy, Helwan University, Egypt.
Arab J Gastroenterol. 2019 Mar;20(1):1-7. doi: 10.1016/j.ajg.2019.01.011. Epub 2019 Mar 7.
Hepatitis C represents a potential public health problem worldwide. Insulin resistance (IR) and type 2 diabetes (T2D) are among the serious metabolic complications for chronic hepatitis C virus (HCV) infection. MicroRNAs (miRNAs) are a group of small non-coding RNAs which are implicated in the modulation of almost all biological processes. The objective of this study was to investigate the levels of both miR-155 and miR-34a in sera of chronic HCV patients with or without T2D.
In this study, we investigated the expression of both miR-155 and miR-34a in 80 subjects (20 HCV, 19 HCV/T2D, 21 T2D and 19 healthy controls), using quantitative real-time PCR.
Our results revealed significantly higher levels of both miR-155 and miR-34a in chronic HCV patients compared to healthy control subjects. However, only circulating miR-155 levels showed significant decline in diabetic HCV patients compared to non-diabetic HCV group. Intriguingly, the circulating levels of miR-155 were inversely correlated with HOMA-IR, fasting blood glucose and HbA1c levels.
Our findings indicate that the insulin resistance and T2D in HCV are strongly related to miR-155. This may suggest a role for miR-155 in the pathogenesis of IR caused by HCV. However, further large-scale studies are required to confirm our findings.
丙型肝炎是全球潜在的公共卫生问题。胰岛素抵抗(IR)和2型糖尿病(T2D)是慢性丙型肝炎病毒(HCV)感染的严重代谢并发症。微小RNA(miRNA)是一组小的非编码RNA,几乎参与所有生物过程的调控。本研究的目的是调查合并或未合并T2D的慢性HCV患者血清中miR-155和miR-34a的水平。
在本研究中,我们使用定量实时PCR检测了80名受试者(20名HCV患者、19名HCV/T2D患者、21名T2D患者和19名健康对照者)中miR-155和miR-34a的表达。
我们的结果显示,与健康对照受试者相比,慢性HCV患者中miR-155和miR-34a的水平显著更高。然而,与非糖尿病HCV组相比,仅糖尿病HCV患者的循环miR-155水平显著下降。有趣的是,miR-155的循环水平与HOMA-IR、空腹血糖和糖化血红蛋白水平呈负相关。
我们的研究结果表明,HCV中的胰岛素抵抗和T2D与miR-155密切相关。这可能表明miR-155在HCV引起的IR发病机制中起作用。然而,需要进一步的大规模研究来证实我们的发现。