Suppr超能文献

通过使用一组选定的循环 microRNAs 进行改良的预防风险分层。

Improved risk stratification in prevention by use of a panel of selected circulating microRNAs.

机构信息

Department of Internal Medicine III, Cardiology, University Hospital, Goethe University Frankfurt, Frankfurt, Germany.

German Centre for Cardiovascular Research (DZHK), Partner site RheinMain, Frankfurt, Germany.

出版信息

Sci Rep. 2017 Jul 3;7(1):4511. doi: 10.1038/s41598-017-04040-w.

Abstract

Risk stratification is crucial in prevention. Circulating microRNAs have been proposed as biomarkers in cardiovascular disease. Here a miR panel consisting of miRs related to different cardiovascular pathophysiologies, was evaluated to predict outcome in the context of prevention. MiR-34a, miR-223, miR-378, miR-499 and miR-133 were determined from peripheral blood by qPCR and combined to a risk panel. As derivation cohort, 178 individuals of the DETECT study, and as validation cohort, 129 individuals of the SHIP study were used in a case-control approach. Overall mortality and cardiovascular events were outcome measures. The Framingham Risk Score(FRS) and the SCORE system were applied as risk classification systems. The identified miR panel was significantly associated with mortality given by a hazard ratio(HR) of 3.0 (95% (CI): 1.09-8.43; p = 0.034) and of 2.9 (95% CI: 1.32-6.33; p = 0.008) after adjusting for the FRS in the derivation cohort. In a validation cohort the miR-panel had a HR of 1.31 (95% CI: 1.03-1.66; p = 0.03) and of 1.29 (95% CI: 1.02-1.64; p = 0.03) in a FRS/SCORE adjusted-model. A FRS/SCORE risk model was significantly improved to predict mortality by the miR panel with continuous net reclassification index of 0.42/0.49 (p = 0.014/0.005). The present miR panel of 5 circulating miRs is able to improve risk stratification in prevention with respect to mortality beyond the FRS or SCORE.

摘要

风险分层在预防中至关重要。循环 microRNAs 已被提议作为心血管疾病的生物标志物。在这里,评估了由与不同心血管病理生理学相关的 mirs 组成的 mir 面板,以预测预防背景下的结果。通过 qPCR 从外周血中测定 miR-34a、miR-223、miR-378、miR-499 和 miR-133,并将其组合成风险面板。在病例对照研究中,使用 DETECT 研究的 178 名个体作为推导队列,SHIP 研究的 129 名个体作为验证队列。总死亡率和心血管事件是结果测量指标。Framingham 风险评分(FRS)和 SCORE 系统被用作风险分类系统。确定的 mir 面板与死亡率显著相关,风险比(HR)为 3.0(95%置信区间:1.09-8.43;p=0.034),在推导队列中调整 FRS 后为 2.9(95%置信区间:1.32-6.33;p=0.008)。在验证队列中,mir 面板的 HR 为 1.31(95%置信区间:1.03-1.66;p=0.03),在 FRS/SCORE 调整模型中为 1.29(95%置信区间:1.02-1.64;p=0.03)。FRS/SCORE 风险模型通过 mir 面板显著改善了死亡率的预测,连续净重新分类指数为 0.42/0.49(p=0.014/0.005)。目前的 5 种循环 mir 面板能够改善预防死亡率的风险分层,超过了 FRS 或 SCORE。

相似文献

1
2
Circulating microRNAs predict future fatal myocardial infarction in healthy individuals - The HUNT study.
J Mol Cell Cardiol. 2016 Aug;97:162-8. doi: 10.1016/j.yjmcc.2016.05.009. Epub 2016 May 15.
3
Increased circulating microRNA-122 is a biomarker for discrimination and risk stratification in patients defined by sepsis-3 criteria.
PLoS One. 2018 May 21;13(5):e0197637. doi: 10.1371/journal.pone.0197637. eCollection 2018.
4
Liver-specific microRNA-122 as prognostic biomarker in patients with chronic systolic heart failure.
Int J Cardiol. 2020 Mar 15;303:80-85. doi: 10.1016/j.ijcard.2019.11.090. Epub 2019 Nov 7.
6
Whole blood sequencing reveals circulating microRNA associations with high-risk traits in non-ST-segment elevation acute coronary syndrome.
Atherosclerosis. 2017 Jun;261:19-25. doi: 10.1016/j.atherosclerosis.2017.03.041. Epub 2017 Mar 30.
7
Identifying circulating microRNAs as biomarkers of cardiovascular disease: a systematic review.
Cardiovasc Res. 2016 Sep;111(4):322-37. doi: 10.1093/cvr/cvw174. Epub 2016 Jun 29.
8
miRNA-197 and miRNA-223 Predict Cardiovascular Death in a Cohort of Patients with Symptomatic Coronary Artery Disease.
PLoS One. 2015 Dec 31;10(12):e0145930. doi: 10.1371/journal.pone.0145930. eCollection 2015.
10
Influence of Overweight and Obesity on Circulating Inflammation-Related microRNA.
Microrna. 2018;7(2):148-154. doi: 10.2174/2211536607666180402120806.

引用本文的文献

3
MicroRNAs and Cardiovascular Disease Risk.
Curr Cardiol Rep. 2024 Feb;26(2):51-60. doi: 10.1007/s11886-023-02014-1. Epub 2024 Jan 11.
5
Circulating MicroRNAs as Novel Biomarkers in Risk Assessment and Prognosis of Coronary Artery Disease.
Eur Cardiol. 2022 Mar 7;17:e06. doi: 10.15420/ecr.2021.47. eCollection 2022 Feb.
8
Cardiorenal Syndrome: New Pathways and Novel Biomarkers.
Biomolecules. 2021 Oct 26;11(11):1581. doi: 10.3390/biom11111581.
9
MiR-223 levels predicting perioperative bleeding in off-pump coronary artery bypass grafting.
Ann Transl Med. 2020 Nov;8(21):1341. doi: 10.21037/atm-20-2022b.
10
Extracellular miRNAs: From Biomarkers to Mediators of Physiology and Disease.
Cell Metab. 2019 Oct 1;30(4):656-673. doi: 10.1016/j.cmet.2019.07.011. Epub 2019 Aug 22.

本文引用的文献

1
MicroRNA-34a Plays a Key Role in Cardiac Repair and Regeneration Following Myocardial Infarction.
Circ Res. 2015 Aug 14;117(5):450-9. doi: 10.1161/CIRCRESAHA.117.305962. Epub 2015 Jun 16.
2
Comparing two correlated C indices with right-censored survival outcome: a one-shot nonparametric approach.
Stat Med. 2015 Feb 20;34(4):685-703. doi: 10.1002/sim.6370. Epub 2014 Nov 17.
3
MicroRNA-378 controls classical brown fat expansion to counteract obesity.
Nat Commun. 2014 Aug 22;5:4725. doi: 10.1038/ncomms5725.
5
Admission levels of circulating miR-499-5p and risk of death in elderly patients after acute non-ST elevation myocardial infarction.
Int J Cardiol. 2014 Mar 15;172(2):e276-8. doi: 10.1016/j.ijcard.2013.12.203. Epub 2014 Jan 8.
7
A cardiac-enriched microRNA, miR-378, blocks cardiac hypertrophy by targeting Ras signaling.
J Biol Chem. 2013 Apr 19;288(16):11216-32. doi: 10.1074/jbc.M112.442384. Epub 2013 Feb 27.
8
MicroRNA-34a regulates cardiac ageing and function.
Nature. 2013 Mar 7;495(7439):107-10. doi: 10.1038/nature11919. Epub 2013 Feb 20.
9
Mortality from ischaemic heart disease by country, region, and age: statistics from World Health Organisation and United Nations.
Int J Cardiol. 2013 Sep 30;168(2):934-45. doi: 10.1016/j.ijcard.2012.10.046. Epub 2012 Dec 4.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验