眼科 ›› 2025, Vol. 34 ›› Issue (5): 389-394.doi: 10.13281/j.cnki.issn.1004-4469.2025.05.010

• 论著 • 上一篇    下一篇

增生性糖尿病视网膜病变血清潜在生物标志物hsa_circ_0000615的发现与验证

张晴1   李婧2   浮娇1   

  1. 1 西安交通大学第一附属医院内分泌代谢科,西安710000; 2 西安交通大学第一附属医院眼科, 西安710000
  • 收稿日期:2024-07-18 出版日期:2025-09-25 发布日期:2025-09-12
  • 通讯作者: 浮姣,Email:jiao_fu@xjtufh.edu.cn
  • 基金资助:
     陕西省科学技术厅社会发展基金(2019SF-490)

Discovery and validation of serum hsa_circ_0000615 as a potential biomarker for proliferative diabetic retinopathy

Zhang Qing1, Li Jing2, Fu Jiao1   

  1. 1 Department of Endocrinology, the First Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710000, China;
    2 Departments of Ophthalmology, the First Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710000, China
  • Received:2024-07-18 Online:2025-09-25 Published:2025-09-12
  • Contact: Fu Jiao, Email: jiao_fu@xjtufh.edu.cn  
  • Supported by:
    Social Development Fund of Shaanxi Provincial Department of Science and Technology (2019SF-490)

摘要:  目的  筛查并确定血清hsa_circ_0000615是否可作为增生性糖尿病视网膜病变(PDR)的新型非侵入性生物标志物。设计  前瞻性病例系列。研究对象  采用简单随机抽样方法选择50例非糖尿病志愿者(对照组)、48例无DR的2型糖尿病(T2DM)患者、50例PDR患者和50例非增生性DR(NPDR)患者。方法  采用高通量全转录组测序以探索血清circRNAs表达谱,并通过定量实时聚合酶链反应(qRT- PCR)验证候选circRNAs。受试者工作特征(ROC)曲线分析评估这些候选circRNAs区分PDR患者与NPDR患者、T2DM患者、对照组的能力。主要指标   血清circRNAs表达谱和has_circ_0000615表达水平。结果   通过测序和qRT-PCR发现PDR患者的hsa_circ_0000615[12.015(8.530,14.325)]较对照组[3.998(3.220,5.156)]、T2DM组[5.118(3.895,7.247)]、NPDR组[5.250(4.045,7.763)]升高(P均<0.05)。PDR患者hsa_circ_0000615表达水平与糖尿病病程(r=0.429,P<0.001)和糖化血红蛋白(HbAc1)水平(r=0.567,P<0.001)呈正相关。血清hsa_circ_0000615在区分PDR患者与NPDR患者、T2DM患者、对照组方面的ROC曲线下面积分别为0.803±0.036(95% CI:0.731~0.874)、0.796±0.039(95% CI:0.719~0.872)、0.976±0.010(95% CI:0.956~0.997)。结论  血清hsa_circ_0000615有望成为眼科影像之外的PDR新型诊断生物标志物和潜在的治疗靶点。  

关键词:  , 环状RNAs;增生性糖尿病视网膜病变;生物标志物

Abstract:   Objective To screen and determine whether serum hsa_circ_0000615 can be used as a new non invasive biomarker for proliferative diabetic retinopathy (PDR). Design Prospective case series. Participants  A simple random sampling method was used to select 50 non-diabetic volunteers (as control group), 48 patients with type-2 diabetes mellitus (T2DM), 50 PDR patients and 50 patients with non-PDR (NPDR). Methods  High throughput whole transcriptome sequencing was performed to explore the expression profile of serum circRNAs, and the candidate circRNAs were validated by quantitative real-time polymerase chain reaction (qRT-PCR). Receiver operating characteristic (ROC) analysis evaluated the ability of serum hsa_circ_0000615 in discriminating PDR patients from NPDR patients, T2DM patients and control subjects. Main Outcome Measures  Serum circRNAs expression profile and has_cic_0000615 expression level. Results  By sequencing and qRT-PCR, serum hsa_circ_0000615 expression in PDR patients [12.015 (8.530, 14.325)] was significantly higher than that in control group [3.998 (3.220, 5.156)], T2DM group [5.118 (3.895, 7.247)] and NPDR group [5.250 (4.045, 7.763)] (all P<0.05).  By correlation analysis and linear regression analysis, the level of hsa_circ_0000615 expression was positively correlated with the course of diabetes (r=0.429, P<0.001) and the level of glycated hemoglobin (r=0.567, P<0.001). ROC curve analysis showed that the area under curve of serum hsa_circ_0000615 was 0.803±0.036 (95% CI: 0.731~0.874), 0.796±0.039 (95% CI: 0.719~0.872) and 0.976±0.010 (95%CI: 0.956~0.997), respectively. Conclusion  The present findings indicate that serum hsa_circ_ 0000615 may serve as a novel diagnostic biomarker and potential therapeutic target for PDR.

Key words:  CircRNAs, Proliferative diabetic retinopathy, Biomarkers