Evaluation of the diagnostic role of circulating miR-16, miR-10b, and miR-21 expression in patients with nonalcoholic fatty liver disease

IF 1 Q4 GENETICS & HEREDITY
Fatemeh Amani , Amirhossein Sahebkar , Seyed Hamid Aghaee-Bakhtiari , Mohammadreza Farzanehfar , Saeedeh Askarian , Reza Kazemi Oskuee
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Abstract

Non-alcoholic fatty liver disease (NAFLD) is a growing global health concern and is characterized by fat accumulation in the liver in the absence of significant alcohol consumption. However, current diagnostic tools, including liver biopsy and imaging techniques, have limitations in terms of accessibility, invasiveness, and sensitivity. Recently, microRNAs (miRNAs) have emerged as non-invasive biomarkers for the diagnosis of NAFLD. In this study, we investigated the expression of three microRNAs (miR-16, miR-10b, and miR-21) in patients with NAFLD across different disease stages compared with healthy subjects. First, miRNAs were extracted from serum samples collected from 34 healthy controls and 38 patients with NAFLD, including 20 with grade 1 and 18 with grade 2 of the disease. Subsequently, cDNA was synthesized from RNA, and miR-21, miR-16, and miR-10b expression was measured using RT-qPCR. The results revealed the downregulation of miR-16 in the early and advanced stages of NAFLD. The serum expression of miR-21 (p < 0 0.01) and miR-10b (p < 0.05) increased in the total NAFLD samples compared with the control group. Moreover, miR-10b expression was significantly higher in patients with stage 2 of NAFLD than in those with stage1 of NAFLD (p < 0.05), suggesting its potential as a biomarker to distinguish between the different grades of the disease. Our results revealed the clinical value of these miRNAs as non-invasive, sensitive, and stage-specific biomarkers for NAFLD. These findings suggest that the assessment of miR-16, miR-21, and miR-10b expression levels could serve as a potentially useful tool for the diagnosis of NAFLD presence and severity.

Abstract Image

评估循环 miR-16、miR-10b 和 miR-21 表达在非酒精性脂肪肝患者中的诊断作用
非酒精性脂肪肝(NAFLD)是一个日益受到全球关注的健康问题,其特点是在没有大量饮酒的情况下肝脏中脂肪堆积。然而,目前的诊断工具,包括肝活检和成像技术,在可及性、侵袭性和灵敏度方面都有局限性。最近,微小核糖核酸(miRNA)已成为诊断非酒精性脂肪肝的非侵入性生物标志物。在这项研究中,我们研究了非酒精性脂肪肝患者在不同疾病阶段与健康人相比的三种微RNA(miR-16、miR-10b和miR-21)的表达情况。首先,我们从 34 名健康对照者和 38 名非酒精性脂肪肝患者(包括 20 名 1 级患者和 18 名 2 级患者)的血清样本中提取了 miRNA。随后,从 RNA 中合成 cDNA,并采用 RT-qPCR 方法测定 miR-21、miR-16 和 miR-10b 的表达。结果显示,在非酒精性脂肪肝的早期和晚期,miR-16 的表达均出现下调。与对照组相比,非酒精性脂肪肝总样本中血清中miR-21(p < 0 0.01)和miR-10b(p < 0.05)的表达增加。此外,非酒精性脂肪肝二期患者的 miR-10b 表达明显高于非酒精性脂肪肝一期患者(p < 0.05),这表明 miR-10b 有可能成为区分疾病不同等级的生物标志物。我们的研究结果揭示了这些 miRNA 作为非侵袭性、敏感性和非酒精性脂肪肝分期特异性生物标志物的临床价值。这些研究结果表明,评估 miR-16、miR-21 和 miR-10b 的表达水平可作为诊断非酒精性脂肪肝的存在和严重程度的潜在有用工具。
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来源期刊
Gene Reports
Gene Reports Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.30
自引率
7.70%
发文量
246
审稿时长
49 days
期刊介绍: Gene Reports publishes papers that focus on the regulation, expression, function and evolution of genes in all biological contexts, including all prokaryotic and eukaryotic organisms, as well as viruses. Gene Reports strives to be a very diverse journal and topics in all fields will be considered for publication. Although not limited to the following, some general topics include: DNA Organization, Replication & Evolution -Focus on genomic DNA (chromosomal organization, comparative genomics, DNA replication, DNA repair, mobile DNA, mitochondrial DNA, chloroplast DNA). Expression & Function - Focus on functional RNAs (microRNAs, tRNAs, rRNAs, mRNA splicing, alternative polyadenylation) Regulation - Focus on processes that mediate gene-read out (epigenetics, chromatin, histone code, transcription, translation, protein degradation). Cell Signaling - Focus on mechanisms that control information flow into the nucleus to control gene expression (kinase and phosphatase pathways controlled by extra-cellular ligands, Wnt, Notch, TGFbeta/BMPs, FGFs, IGFs etc.) Profiling of gene expression and genetic variation - Focus on high throughput approaches (e.g., DeepSeq, ChIP-Seq, Affymetrix microarrays, proteomics) that define gene regulatory circuitry, molecular pathways and protein/protein networks. Genetics - Focus on development in model organisms (e.g., mouse, frog, fruit fly, worm), human genetic variation, population genetics, as well as agricultural and veterinary genetics. Molecular Pathology & Regenerative Medicine - Focus on the deregulation of molecular processes in human diseases and mechanisms supporting regeneration of tissues through pluripotent or multipotent stem cells.
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