He Ling, Wu Xingwu, Wu Rongye, Guo Ping, He Wenfeng, Sun Wanlei, Chen He
Department of Geratology, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi 330006, P.R. China.
Assisted Reproductive Center, Jiangxi Maternal and Child Health Hospital, Nanchang, Jiangxi 330006, P.R. China.
Exp Ther Med. 2022 May;23(5):347. doi: 10.3892/etm.2022.11275. Epub 2022 Mar 23.
Asthenozoospermia (AZS) is characterized by reduced sperm motility and its pathogenesis remains poorly understood. Piwi-interacting RNAs (piRNAs) have been indicated to serve important roles in spermatogenesis. However, little is known about the correlation of piRNA expression with AZS. In the present study, small RNA sequencing (small RNA-seq) was performed on sperm samples from AZS patients and fertile controls. Reverse transcription-quantitative (RT-q) PCR was used to validate the small RNA-seq results. Bioinformatics analyses were performed to predict the functions of differentially expressed piRNAs (DEpiRNAs). Logistic regression models were constructed and receiver operating characteristic curve (ROC) analysis was used to evaluate their diagnostic performance. A total of 114 upregulated and 169 downregulated piRNAs were detected in AZS patients. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes analyses showed that the DEpiRNAs were mainly associated with transcription, signal transduction, cell differentiation, metal ion binding and focal adhesion. These results were verified by RT-qPCR analysis of eight selected piRNAs. The PCR results were consistent with the sequencing results in patients with AZS compared with controls in the first cohort. The expression of piR-hsa-32694, piR-hsa-26591, piR-hsa-18725 and piR-hsa-18586 was significantly upregulated in patients with AZS. The diagnostic power of the four piRNAs was further analyzed using ROC analysis; piR-hsa-26591 exhibited an area under the ROC curve (AUC) of 0.913 (95% CI: 0.795-0.994). Logistic regression modelling and subsequent ROC analysis indicated that the combination of the 4 piRNAs achieved good diagnostic efficacy (AUC: 0.935).
弱精子症(AZS)的特征是精子活力降低,其发病机制仍知之甚少。已有研究表明,Piwi相互作用RNA(piRNA)在精子发生中起重要作用。然而,关于piRNA表达与AZS的相关性却知之甚少。在本研究中,对AZS患者和正常生育对照者的精子样本进行了小RNA测序(small RNA-seq)。采用逆转录定量(RT-q)PCR验证小RNA-seq结果。进行生物信息学分析以预测差异表达的piRNA(DEpiRNA)的功能。构建逻辑回归模型,并使用受试者工作特征曲线(ROC)分析来评估其诊断性能。在AZS患者中总共检测到114个上调的piRNA和169个下调的piRNA。基因本体论和京都基因与基因组百科全书分析表明,DEpiRNA主要与转录、信号转导、细胞分化、金属离子结合和粘着斑有关。通过对8个选定piRNA的RT-qPCR分析验证了这些结果。在第一个队列中,与对照组相比,AZS患者的PCR结果与测序结果一致。piR-hsa-32694、piR-hsa-26591、piR-hsa-18725和piR-hsa-18586在AZS患者中的表达显著上调。使用ROC分析进一步分析了这4种piRNA的诊断能力;piR-hsa-