非编码RNA在急性主动脉夹层中的调控:从特征到机制。

IF 3.4 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Ruibin Wei, Yingqing Feng
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引用次数: 0

摘要

主动脉夹层是一种危及生命的疾病,由主动脉内膜撕裂或主动脉壁出血引起,导致主动脉壁层分离。正如Nienaber所报道的,主动脉夹层在65-75岁的人群中最常见,在这一人群中,每年每10万人中有35例发生。主动脉夹层的发病因素很多,包括高血压、血脂异常、遗传变异引起的主动脉内膜异常等。然而,随着基因测序和转基因技术的发展,基因方法正被用于疾病的诊断和治疗,包括急性主动脉夹层。关于急性主动脉夹层的基因研究始于2006年左右。近年来,对急性主动脉夹层的研究主要集中在microRNA (miRNA)上。研究发现,miRNA在急性主动脉夹层的发生发展中起着至关重要的调节作用。通过调节miRNA的表达,可以预防和治疗急性主动脉夹层。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Noncoding RNA in the Regulation of Acute Aortic Dissection: From Profile to Mechanism

Aortic dissection is a life-threatening condition caused by a tear in the intimal layer of the aorta or bleeding within the aortic wall, resulting in the separation of the layers of the aortic wall. As Nienaber reported, aortic dissection is most common in people 65–75 years old and has an incidence of 35 cases per 100,000 people per year in this population. Many pathogenic factors are involved in aortic dissection, including hypertension, dyslipidemia, and abnormality of the aortic intima caused by genetic variation. However, with the development of gene sequencing and transgenic technology, genetic methods are being used for the diagnosis and treatment of diseases, including acute aortic dissection. Genetic research on acute aortic dissection began around 2006. Recently, research on acute aortic dissection has mainly focused on microRNA (miRNA). Studies have found that miRNA plays a critical regulatory role in the occurrence and development of acute aortic dissection. By regulating miRNA expression, acute aortic dissection can be prevented and treated.

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来源期刊
Cardiovascular Therapeutics
Cardiovascular Therapeutics 医学-心血管系统
CiteScore
5.60
自引率
0.00%
发文量
55
审稿时长
6 months
期刊介绍: Cardiovascular Therapeutics (formerly Cardiovascular Drug Reviews) is a peer-reviewed, Open Access journal that publishes original research and review articles focusing on cardiovascular and clinical pharmacology, as well as clinical trials of new cardiovascular therapies. Articles on translational research, pharmacogenomics and personalized medicine, device, gene and cell therapies, and pharmacoepidemiology are also encouraged. Subject areas include (but are by no means limited to): Acute coronary syndrome Arrhythmias Atherosclerosis Basic cardiac electrophysiology Cardiac catheterization Cardiac remodeling Coagulation and thrombosis Diabetic cardiovascular disease Heart failure (systolic HF, HFrEF, diastolic HF, HFpEF) Hyperlipidemia Hypertension Ischemic heart disease Vascular biology Ventricular assist devices Molecular cardio-biology Myocardial regeneration Lipoprotein metabolism Radial artery access Percutaneous coronary intervention Transcatheter aortic and mitral valve replacement.
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