血浆来源的细胞外小泡转录组学分析揭示了正常紧张性青光眼的病理特征。

Extracellular vesicles and circulating nucleic acids Pub Date : 2024-08-19 eCollection Date: 2024-01-01 DOI:10.20517/evcna.2024.45
Sheng-Lan Xu, Jun-Hua Li, Wen-Meng Zhang, Meng-Jun Fu, Hui-Min Xing, Hua Ma, Xian-Hui Gong, Rong-Han Wu, Yuan-Bo Liang, Ren-Zhe Cui, Zai-Long Chi
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引用次数: 0

摘要

目的:正常张力性青光眼(NTG)是一种常见的视神经病变,由于眼压保持在正常范围内,诊断具有挑战性。早期诊断和干预对患者的有效终身管理至关重要。方法:本研究共招募225名受试者。通过转录组测序分析循环血浆中的小细胞外囊泡(sEVs) RNA,并通过定量实时聚合酶链反应(qRT-PCR)验证其表达水平。采用Logistic回归、线性回归和受试者工作特征(ROC)曲线分析来检验生物标志物与临床病理特征的相关性。结果:NTG患者sEVs mrna分析显示线粒体功能障碍,中枢神经系统退行性通路富集,反映了NTG的病理特征。与对照组相比,NTG患者血浆中sev let-7b-5p的表达水平明显降低,曲线下面积(AUC)为0.870 (95%CI: 0.797-0.943) (P < 0.0001),与年龄相关的AUC为0.923 (95%CI: 0.851-0.996) (P < 0.0001)。此外,我们发现let-7b-5p水平与NTG患者的严重程度和视野缺损有显著相关性,与其他眼科疾病相比具有良好的特异性。结论:NTG循环血浆中sev RNA特征揭示了线粒体功能障碍,sev let-7b-5p可作为NTG有用的无创生物标志物。
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Transcriptomic analysis of plasma-derived small extracellular vesicles reveals the pathological characteristics of normal tension glaucoma.

Aim: Normal tension glaucoma (NTG) is a common optic neuropathy that can be challenging to diagnose due to the intraocular pressure remaining within the normal range. Early diagnosis and intervention are crucial for the effective lifelong management of patients.

Methods: This study recruited a total of 225 participants. Small extracellular vesicles (sEVs) RNA from circulating plasma was analyzed via transcriptomic sequencing, and its expression levels were verified by quantitative real-time polymerase chain reaction (qRT-PCR). Logistic regression, linear regression, and receiver operating characteristic (ROC) curve analyses were performed to examine the association of biomarkers with clinicopathological characteristics.

Results: Analysis of sEVs mRNAs in NTG patients revealed mitochondrial dysfunction and enrichment of central nervous system degenerative pathways, reflecting the pathological features of NTG. Compared with those in the controls, the expression levels of sEVs let-7b-5p in the plasma of NTG patients were significantly lower, with an area under the curve (AUC) of 0.870 (95%CI: 0.797-0.943) (P < 0.0001), and the AUC combined with age was 0.923 (95%CI: 0.851-0.996) (P < 0.0001). In addition, we found that let-7b-5p levels were significantly correlated with the severity and visual field defects of NTG patients and had good specificity compared with other ophthalmic diseases.

Conclusion: The sEVs RNA signatures in circulating plasma from NTG revealed mitochondrial dysfunction and that sEVs let-7b-5p can be a useful noninvasive biomarker for NTG.

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