Centre for Advanced Research and Excellence in Heart Failure (CARE-HF), Sree Chitra Tirunal Institute for Medical Sciences and Technology (SCTIMST), Trivandrum 695011, Kerala, India.
Centre for Advanced Research and Excellence in Heart Failure (CARE-HF), Sree Chitra Tirunal Institute for Medical Sciences and Technology (SCTIMST), Trivandrum 695011, Kerala, India; Department of Cardiology, Sree Chitra Tirunal Institute for Medical Sciences and Technology (SCTIMST), Trivandrum 695011, Kerala, India.
Int J Biol Macromol. 2024 Mar;261(Pt 2):129714. doi: 10.1016/j.ijbiomac.2024.129714. Epub 2024 Jan 27.
MicroRNAs (miRNAs), a class of non-coding RNAs, are utilized as biomarkers for a wide range of disorders. Circulating miRNAs are proposed as potential markers in the clinical identification of heart failure (HF). However, identifying miRNA biomarkers in HF requires identification of robust endogenous control miRNAs for normalization in differential expression analysis. Hence, this study aimed to identify circulating miRNAs that can be utilized as endogenous controls in HF. We evaluated the expression of eight miRNAs, which were previously reported as endogenous controls in different pathological conditions. Total RNA, including miRNA, was extracted from the serum samples of 30 HF patients (15 HFrEF and 15 HFpEF) and their matched controls (n = 15). We used quantitative PCR to determine the miRNA expression. The stability of the selected endogenous miRNAs was assessed and compared using a standard set of criteria with the RefFinder software. Six of the eight miRNAs analyzed showed consistent expression among all sample groups. Stability analysis ranked hsa-let-7i-5p, hsa-miR-148b-3p, and hsa-miR-484 as the most stable miRNAs, indicating their potential as reliable endogenous controls.
微小 RNA(miRNAs)是一类非编码 RNA,被用作多种疾病的生物标志物。循环 miRNAs 被认为是心力衰竭(HF)临床诊断的潜在标志物。然而,要在 HF 中识别 miRNA 生物标志物,需要鉴定用于差异表达分析的稳健内源性对照 miRNA。因此,本研究旨在鉴定可作为 HF 内源性对照的循环 miRNA。我们评估了 8 种 miRNA 的表达情况,这些 miRNA 之前曾在不同的病理条件下被报道为内源性对照。从 30 名 HF 患者(15 名 HFrEF 和 15 名 HFpEF)及其匹配的对照组(n=15)的血清样本中提取包括 miRNA 在内的总 RNA。我们使用定量 PCR 来确定 miRNA 的表达。使用 RefFinder 软件,根据一套标准标准评估并比较了选定的内源性 miRNA 的稳定性。在所有样本组中,分析的 8 个 miRNA 中的 6 个显示出一致的表达。稳定性分析将 hsa-let-7i-5p、hsa-miR-148b-3p 和 hsa-miR-484 列为最稳定的 miRNA,表明它们有作为可靠内源性对照的潜力。