Smith Michael A, Chiacchia Sam, Boehme Jason, Datar Sanjeev A, Morell Emily, Keller Roberta L, Romer Amy, Colglazier Elizabeth, Parker Claire, Becerra Jasmine, Fineman Jeffrey R
Division of Pediatric Critical Care, Department of Pediatrics, University of California, San Francisco, California, United States.
Division of Pediatric Pulmonary Hypertension, Department of Pediatrics, University of California, San Francisco, California, United States.
Am J Physiol Heart Circ Physiol. 2025 Jan 1;328(1):H47-H57. doi: 10.1152/ajpheart.00622.2024. Epub 2024 Nov 26.
Pediatric pulmonary hypertension is a heterogeneous disease associated with significant morbidity and mortality. MicroRNAs have been implicated as both pathologic drivers of disease and potential therapeutic targets in pediatric pulmonary hypertension. We sought to characterize the circulating microRNA profiles of a diverse array of pediatric patients with pulmonary hypertension using high-throughput sequencing technology. Peripheral blood samples were drawn from patients recruited at the time of a clinically indicated cardiac catheterization, and microRNA sequencing followed by differential expression and target/pathway enrichment analyses were performed. Among 63 pediatric patients with pulmonary hypertension, we identified specific microRNA signatures that uniquely classified patients by disease subtype, correlated with indicators of disease severity including invasive hemodynamic metrics, and changed over the course of treatment for pulmonary hypertension. These microRNA profiles include a number of specific microRNA molecules known to function in signaling pathways critical to pulmonary vascular biology and disease, including transforming growth factor-β (TGF-β), VEGF, PI3K/Akt, cGMP-PKG, and HIF-1 signaling. Circulating levels of miR-122-5p, miR-124-3p, miR-204-5p, and miR-9-5p decreased over the course of treatment in a subset of patients who had multiple samples drawn during the study period. Our findings support the further investigation of specific microRNAs as mechanistic mediators, biomarkers, and therapeutic targets in pulmonary hypertension. We present novel insight into the circulating microRNA profiles of pediatric patients with pulmonary hypertension. Our findings support the utility of microRNAs as both useful biomarkers of disease severity and potential therapeutic targets in pediatric pulmonary hypertension.
小儿肺动脉高压是一种异质性疾病,具有较高的发病率和死亡率。微小RNA已被认为是小儿肺动脉高压疾病的病理驱动因素和潜在治疗靶点。我们试图使用高通量测序技术来表征一系列不同类型小儿肺动脉高压患者的循环微小RNA谱。在临床指征的心脏导管插入术时采集招募患者的外周血样本,然后进行微小RNA测序,接着进行差异表达以及靶标/通路富集分析。在63例小儿肺动脉高压患者中,我们鉴定出特定的微小RNA特征,这些特征可根据疾病亚型对患者进行独特分类,与包括有创血流动力学指标在内的疾病严重程度指标相关,并在肺动脉高压治疗过程中发生变化。这些微小RNA谱包括许多已知在对肺血管生物学和疾病至关重要的信号通路中起作用的特定微小RNA分子,包括转化生长因子-β(TGF-β)、血管内皮生长因子(VEGF)、磷脂酰肌醇-3激酶/蛋白激酶B(PI3K/Akt)、环磷酸鸟苷-蛋白激酶G(cGMP-PKG)和缺氧诱导因子-1(HIF-1)信号通路。在研究期间采集了多个样本的一部分患者中,miR-122-5p、miR-124-3p、miR-204-5p和miR-9-5p的循环水平在治疗过程中下降。我们的研究结果支持进一步研究特定的微小RNA作为肺动脉高压的机制介导物、生物标志物和治疗靶点。我们对小儿肺动脉高压患者的循环微小RNA谱提出了新的见解。我们的研究结果支持微小RNA作为小儿肺动脉高压疾病严重程度的有用生物标志物和潜在治疗靶点的实用性。