循环 miRNA 在骨质疏松症诊断中的作用 miRNA 在骨质疏松症中的作用。

Revista da Associacao Medica Brasileira (1992) Pub Date : 2024-09-16 eCollection Date: 2024-01-01 DOI:10.1590/1806-9282.20231724
Senay Balci, Nurdan Orucoglu, Didem Derici Yildirim, Cagri Eroglan, Özlem Bolgen Cimen, Lulufer Tamer, Mehmet Burak Yavuz Cimen
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引用次数: 0

摘要

目的:骨质疏松症是一种全身性骨骼疾病,其特点是骨脆性和骨折风险增加。研究表明,miRNAs 的功能失调或其介导的机制可能是导致骨质退化的重要病理因素。因此,本研究旨在确定被认为在骨代谢中发挥作用的 miRNA 在骨质疏松症中的作用:研究对象包括根据定量计算机断层扫描骨矿密度评估结果确诊为骨质疏松症的 48 名患者和 36 名健康人。使用 miRNA 分离试剂盒从乙二胺四乙酸(EDTA)试管中提取的血浆样本中分离出 miRNA,并将其转化为 cDNA。利用实时 PCR(RT-PCR)装置对 miR-21-5p、miR-34a-5p、miR-210、miR-122-5p、miR-125b-5p、miR-133a、miR-143-3p、miR-146a、miR-155-5p 和 miR-223 进行表达分析:结果:将患者组与对照组的 miRNA 表达水平进行比较,发现患者的所有 miRNA 均出现下调。在研究患者组表达水平的折叠变化时,发现 miR-21-5p、miR-133a、mir143-3p、miR-210 和 miR-223 存在显著差异。在接收者操作曲线分析中,miR-34、miR-125、miR-133 和 miR-210 组合的曲线下面积=0.882:本研究确定,miRNA 的联合效应及其单一效应对骨质疏松症的发生均有效。因此,即将建立的 miRNA 小组可为开发治疗骨质疏松症的新型诊断和治疗方法做出重大贡献。
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The role of circulating miRNAs in the diagnosis of osteoporosis miRNAs in osteoporosis.

Objective: Osteoporosis, defined as a systemic skeletal disease, is characterized by increased bone fragility and fracture risk. Studies have shown that dysregulation of the functions of miRNAs or the mechanisms they mediate may be an important pathological factor in bone degeneration. Therefore, the aim of the study was to determine the role of miRNAs, which are thought to play a role in bone metabolism, in osteoporosis.

Methods: The study included 48 patients who were diagnosed with osteoporosis according to the results of a bone mineral density assessment by quantitative computed tomography and 36 healthy individuals. MiRNAs from plasma samples obtained from blood samples taken into ethylenediaminetetraacetic acid (EDTA) tubes were isolated with the miRNA isolation kit and converted to cDNA. Expression analysis of miR-21-5p, miR-34a-5p, miR-210, miR-122-5p, miR-125b-5p, miR-133a, miR-143-3p, miR-146a, miR-155-5p, and miR-223 was performed on the real-time PCR (RT-PCR) device.

Results: When miRNA expression levels in the patient group were compared with the control group, all miRNAs were found to be downregulated in the patients. When fold changes in expression levels in the patient group were examined, significant differences were found in miR-21-5p, miR-133a, mir143-3p, miR-210, and miR-223. In the receiver operating curve analysis, area under the curve=0.882 for the combination of miR-34, miR-125, miR-133, and miR-210.

Conclusion: In this study, it was determined that the combined effects of miRNAs, as well as their single effects, were effective in the development of osteoporosis. Therefore, a miRNA panel to be created can make a significant contribution to the development of novel diagnostic and treatment approaches for this disease.

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