• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

循环血清 miR-509-3p 在先天性心脏病相关肺动脉高压中的临床诊断价值。

Clinical diagnostic value of circulating serum miR-509-3p in pulmonary arterial hypertension with congenital heart disease.

机构信息

Department of Cardiovascular Surgery, Liaocheng People's Hospital, Liaocheng 252000, China.

出版信息

Hellenic J Cardiol. 2020 Jan-Feb;61(1):26-30. doi: 10.1016/j.hjc.2018.06.004. Epub 2018 Jun 8.

DOI:10.1016/j.hjc.2018.06.004
PMID:29890280
Abstract

OBJECTIVE

Most pulmonary arterial hypertension (PAH) biomarkers are used for risk stratification and prognosis prediction. We aimed to evaluate the diagnostic value of circulating serum miR-509-3p in PAH with congenital heart disease.

METHODS

Preoperative blood samples were collected from patients who were diagnosed as having PAH and had to receive right ventricular catheterization. According to right ventricular catheterization results, these patients were divided into a control group with normal mean pulmonary artery pressure (mPAP < 20 mmHg) and a PAH group (mPAP ≥ 25 mmHg). The expression of serum miR-509-3p was detected by real-time quantitative PCR. The receiver operating characteristic curve was plotted. A dichotomous logistic regression model was also established.

RESULTS

The expression level of circulating serum miR-509-3p in the PAH group was significantly lower than that of the control group. Based on the relative expression of miR-509-3p in serum, the area under the curve (AUC) for single-factor diagnosis of PAH was 0.694 (95% confidence interval [CI]: 0.555-0.883, P = 0.01), which was approximately 0.81 (AUC of noninvasive screening by echocardiography). When the relative expression of miR-509-3p was 0.79, the sensitivity and specificity were 80% and 60%, respectively. Based on the established model, AUC of serum miR-509-3p combined with echocardiography was 0.844, thus indicating a high diagnostic value. Compared with two individual indices, the combination further enhanced the diagnostic efficiency.

CONCLUSIONS

The expression of miR-509-3p decreased in the serum of patients with PAH along with congenital heart disease. The diagnostic value of circulating serum miR-509-3p in PAH was close to that obtained by echocardiography. Combining the two indices further increased the diagnostic efficiency of PAH.

摘要

目的

大多数肺动脉高压(PAH)生物标志物用于风险分层和预后预测。本研究旨在评估循环血清 miR-509-3p 在先天性心脏病合并 PAH 中的诊断价值。

方法

收集术前经右心导管检查诊断为 PAH 且必须接受右心导管检查的患者的血液样本。根据右心导管检查结果,将这些患者分为对照组(平均肺动脉压(mPAP)<20mmHg)和 PAH 组(mPAP≥25mmHg)。采用实时定量 PCR 检测血清 miR-509-3p 的表达。绘制受试者工作特征曲线。还建立了二项逻辑回归模型。

结果

PAH 组循环血清 miR-509-3p 的表达水平明显低于对照组。基于血清中 miR-509-3p 的相对表达,PAH 的单因素诊断曲线下面积(AUC)为 0.694(95%置信区间[CI]:0.555-0.883,P=0.01),接近超声心动图无创筛查的 0.81(AUC)。当 miR-509-3p 的相对表达为 0.79 时,敏感性和特异性分别为 80%和 60%。基于建立的模型,血清 miR-509-3p 与超声心动图联合的 AUC 为 0.844,表明具有较高的诊断价值。与两个单独的指标相比,联合进一步提高了诊断效率。

结论

先天性心脏病合并 PAH 患者血清中 miR-509-3p 的表达降低。循环血清 miR-509-3p 在 PAH 中的诊断价值与超声心动图相当。联合这两个指标进一步提高了 PAH 的诊断效率。

相似文献

1
Clinical diagnostic value of circulating serum miR-509-3p in pulmonary arterial hypertension with congenital heart disease.循环血清 miR-509-3p 在先天性心脏病相关肺动脉高压中的临床诊断价值。
Hellenic J Cardiol. 2020 Jan-Feb;61(1):26-30. doi: 10.1016/j.hjc.2018.06.004. Epub 2018 Jun 8.
2
Serum miR-204 and miR-451 Expression and Diagnostic Value in Patients with Pulmonary Artery Hypertension Triggered by Congenital Heart Disease.血清 miR-204 和 miR-451 表达与先天性心脏病相关肺动脉高压患者的诊断价值。
Comput Math Methods Med. 2022 Jun 13;2022:9430708. doi: 10.1155/2022/9430708. eCollection 2022.
3
Circulating microRNA as a Novel Biomarker for Pulmonary Arterial Hypertension Due to Congenital Heart Disease.循环微RNA作为先天性心脏病所致肺动脉高压的新型生物标志物
Pediatr Cardiol. 2017 Jan;38(1):86-94. doi: 10.1007/s00246-016-1487-3. Epub 2016 Nov 11.
4
Expression and clinical significance of miR-8078 in patients with congenital heart disease-associated pulmonary arterial hypertension.miR-8078 在先天性心脏病相关肺动脉高压患者中的表达及临床意义。
Gene. 2024 Feb 20;896:147964. doi: 10.1016/j.gene.2023.147964. Epub 2023 Nov 4.
5
miR-1226-3p Promotes eNOS Expression of Pulmonary Arterial Endothelial Cells to Mitigate Hypertension in Rats via Targeting Profilin-1.miR-1226-3p 通过靶向 Profilin-1 促进肺动脉内皮细胞中 eNOS 的表达,从而减轻大鼠高血压。
Biomed Res Int. 2021 Nov 3;2021:1724722. doi: 10.1155/2021/1724722. eCollection 2021.
6
[Risk factors for death and the clinical features of different subtypes of patients with pulmonary arterial hypertension related to congenital heart disease].[先天性心脏病相关肺动脉高压患者不同亚型的死亡危险因素及临床特征]
Zhonghua Xin Xue Guan Bing Za Zhi. 2020 Apr 24;48(4):315-322. doi: 10.3760/cma.j.cn112148-20190628-00364.
7
Transpulmonary Expression of Exosomal microRNAs in Idiopathic and Congenital Heart Disease-Related Pulmonary Arterial Hypertension.跨肺表达外泌体 microRNAs 在特发性和先天性心脏病相关肺动脉高压中的作用。
J Am Heart Assoc. 2023 Dec 5;12(23):e031435. doi: 10.1161/JAHA.123.031435. Epub 2023 Nov 28.
8
Plasma Connective Tissue Growth Factor as a Biomarker of Pulmonary Arterial Hypertension Associated With Congenital Heart Disease in Adults.血浆结缔组织生长因子作为成人先天性心脏病相关肺动脉高压的生物标志物
Circ J. 2023 Mar 24;87(4):527-535. doi: 10.1253/circj.CJ-22-0172. Epub 2023 Feb 25.
9
miR-29a-3p/THBS2 Axis Regulates PAH-Induced Cardiac Fibrosis.miR-29a-3p/THBS2 轴调控肺动脉高压诱导的心脏纤维化。
Int J Mol Sci. 2021 Sep 30;22(19):10574. doi: 10.3390/ijms221910574.
10
[Value of serum miR-155-5p and miR-133a-3p expression for the diagnosis and prognosis evaluation of sepsis].血清miR-155-5p和miR-133a-3p表达对脓毒症诊断及预后评估的价值
Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2016 Aug;28(8):694-8. doi: 10.3760/cma.j.issn.2095-4352.2016.08.005.

引用本文的文献

1
Dysregulation of miR-330-3p is Involved in the Occurrence and Development of Pulmonary Arterial Hypertension Caused by Congenital Heart Disease.miR-330-3p失调参与先天性心脏病所致肺动脉高压的发生发展。
Anatol J Cardiol. 2025 Apr 21;29(6):291-9. doi: 10.14744/AnatolJCardiol.2025.4807.
2
MicroRNA Expression in Patients with Coronary Artery Disease and Hypertension-A Systematic Review.冠心病合并高血压患者的 microRNA 表达:系统综述。
Int J Mol Sci. 2024 Jun 11;25(12):6430. doi: 10.3390/ijms25126430.
3
Predictive Value of Smoking Index Combined with NT-proBNP for Patients with Pulmonary Hypertension Due to Chronic Lung Disease: A Retrospective Study.
吸烟指数联合 NT-proBNP 对慢性肺部疾病相关肺动脉高压患者的预测价值:一项回顾性研究。
Int J Chron Obstruct Pulmon Dis. 2024 Jun 4;19:1233-1245. doi: 10.2147/COPD.S448496. eCollection 2024.
4
Recent progress in the roles of microRNAs in pulmonary arterial hypertension associated with congenital heart disease.微小 RNA 在先天性心脏病相关肺动脉高压中的作用的最新进展。
Narra J. 2024 Apr;4(1):e579. doi: 10.52225/narra.v4i1.579. Epub 2024 Feb 28.
5
Differential expression spectrum and targeted gene prediction of tRNA-derived small RNAs in idiopathic pulmonary arterial hypertension.特发性肺动脉高压中tRNA衍生小RNA的差异表达谱及靶向基因预测
Front Mol Biosci. 2023 Jul 11;10:1204740. doi: 10.3389/fmolb.2023.1204740. eCollection 2023.
6
Pulmonary arterial hypertension associated with congenital heart disease: An omics study.先天性心脏病相关肺动脉高压:一项组学研究。
Front Cardiovasc Med. 2023 Mar 10;10:1037357. doi: 10.3389/fcvm.2023.1037357. eCollection 2023.
7
Effects of (L.) Sch Bip on colitis-associated colorectal cancer.(L.)Sch Bip对结肠炎相关结直肠癌的影响。
Front Pharmacol. 2023 Jan 9;13:1119091. doi: 10.3389/fphar.2022.1119091. eCollection 2022.
8
Differential Expression Profile of microRNAs and Tight Junction in the Lung Tissues of Rat With Mitomycin-C-Induced Pulmonary Veno-Occlusive Disease.丝裂霉素C诱导的大鼠肺静脉闭塞病肺组织中微小RNA与紧密连接的差异表达谱
Front Cardiovasc Med. 2022 Feb 16;9:746888. doi: 10.3389/fcvm.2022.746888. eCollection 2022.
9
MicroRNA Alterations Induced in Human Skin by Diesel Fumes, Ozone, and UV Radiation.柴油烟雾、臭氧和紫外线辐射对人体皮肤中微小RNA的影响。
J Pers Med. 2022 Jan 28;12(2):176. doi: 10.3390/jpm12020176.
10
miR-29a-3p/THBS2 Axis Regulates PAH-Induced Cardiac Fibrosis.miR-29a-3p/THBS2 轴调控肺动脉高压诱导的心脏纤维化。
Int J Mol Sci. 2021 Sep 30;22(19):10574. doi: 10.3390/ijms221910574.