A comparison of the expression patterns and diagnostic capability of the ncRNAs NEAT1 and miR-34a in non-obstructive azoospermia and severe oligospermia.

IF 3.8 3区 医学 Q2 GENETICS & HEREDITY
Aya Salman, Abdullah F Radwan, Olfat G Shaker, Adel A, Ghadir A Sayed
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引用次数: 0

Abstract

Infertility is a major global health problem, affecting 8-12% of couples worldwide, with male causes contributing to approximately 50% of cases. Notably, around 15% of infertile men are azoospermic. Consequently, there is a critical necessity to find noninvasive biomarkers to help in diagnosing and assessing the susceptibility of patients with various infertility disorders. This study is designed to determine the roles of NEAT1 and miR-34a as diagnostic and susceptibility biomarkers for non-obstructive azoospermia and severe oligospermia. The interactions between these non-coding RNA (ncRNAs) were explored, along with their correlations to hormonal profiles and clinical parameters like sperm count and motility. The potential of serum NEAT1 and miR-34a as diagnostic biomarkers for these conditions was explored. The study included 100 participants: 40 non-obstructive azoospermia patients, 40 severe oligospermia patients, and 20 healthy controls. Quantitative real-time PCR and transcriptomics-based bioinformatics tools were employed to explore the co-expression networks and molecular interactions of NEAT1, miR-34a, SIRT1, and their associated hormonal and genetic pathways. Results indicated that NEAT1 was significantly downregulated in severe oligospermia patients, while its levels in non-obstructive azoospermia patients did not differ significantly from healthy controls. Furthermore, serum miR-34a expression was considerably upregulated in both patient groups compared to controls. This study highlights the promise of serum NEAT1 and miR-34a as diagnostic markers for non-obstructive azoospermia and severe oligospermia. These findings provide valuable insights into male infertility and indicate potential avenues for personalized treatment strategies.

ncRNAs NEAT1和miR-34a在非阻塞性无精子症和严重少精子症中的表达模式和诊断能力的比较
不孕症是一个重大的全球健康问题,影响到全世界8-12%的夫妇,其中男性原因造成约50%的病例。值得注意的是,大约15%的不育男性是无精子症。因此,迫切需要寻找无创生物标志物来帮助诊断和评估各种不孕症患者的易感性。本研究旨在确定NEAT1和miR-34a作为非阻塞性无精子症和严重少精子症的诊断和易感性生物标志物的作用。研究人员探索了这些非编码RNA (ncRNAs)之间的相互作用,以及它们与激素谱和临床参数(如精子数量和活力)的相关性。研究人员探索了血清NEAT1和miR-34a作为这些疾病的诊断性生物标志物的潜力。该研究包括100名参与者:40名非阻塞性无精子症患者,40名严重少精子症患者和20名健康对照。采用实时定量PCR和基于转录组学的生物信息学工具,探索NEAT1、miR-34a、SIRT1及其相关激素和遗传途径的共表达网络和分子相互作用。结果表明,NEAT1在严重少精症患者中显著下调,而在非阻塞性无精症患者中其水平与健康对照组无显著差异。此外,与对照组相比,两组患者血清miR-34a表达均显著上调。这项研究强调了血清NEAT1和miR-34a作为非阻塞性无精子症和严重少精子症的诊断标志物的前景。这些发现为男性不育症提供了有价值的见解,并指出了个性化治疗策略的潜在途径。
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来源期刊
Human Genomics
Human Genomics GENETICS & HEREDITY-
CiteScore
6.00
自引率
2.20%
发文量
55
审稿时长
11 weeks
期刊介绍: Human Genomics is a peer-reviewed, open access, online journal that focuses on the application of genomic analysis in all aspects of human health and disease, as well as genomic analysis of drug efficacy and safety, and comparative genomics. Topics covered by the journal include, but are not limited to: pharmacogenomics, genome-wide association studies, genome-wide sequencing, exome sequencing, next-generation deep-sequencing, functional genomics, epigenomics, translational genomics, expression profiling, proteomics, bioinformatics, animal models, statistical genetics, genetic epidemiology, human population genetics and comparative genomics.
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