应对心脏代谢疾病的新技术、生物标志物和分子靶点

Novel Techniques, Biomarkers and Molecular Targets to Address Cardiometabolic Diseases.

作者信息

Di Fiore Valerio, Cappelli Federica, Del Punta Lavinia, De Biase Nicolò, Armenia Silvia, Maremmani Davide, Lomonaco Tommaso, Biagini Denise, Lenzi Alessio, Mazzola Matteo, Tricò Domenico, Masi Stefano, Mengozzi Alessandro, Pugliese Nicola Riccardo

机构信息

Department of Clinical and Experimental Medicine, University of Pisa, Via Roma 67, 56124 Pisa, Italy.

Department of Chemistry and Industrial Chemistry, University of Pisa, Via Giuseppe Moruzzi 13, 56124 Pisa, Italy.

出版信息

J Clin Med. 2024 May 14;13(10):2883. doi: 10.3390/jcm13102883.

Abstract

Cardiometabolic diseases (CMDs) are interrelated and multifactorial conditions, including arterial hypertension, type 2 diabetes, heart failure, coronary artery disease, and stroke. Due to the burden of cardiovascular morbidity and mortality associated with CMDs' increasing prevalence, there is a critical need for novel diagnostic and therapeutic strategies in their management. In clinical practice, innovative methods such as epicardial adipose tissue evaluation, ventricular-arterial coupling, and exercise tolerance studies could help to elucidate the multifaceted mechanisms associated with CMDs. Similarly, epigenetic changes involving noncoding RNAs, chromatin modulation, and cellular senescence could represent both novel biomarkers and targets for CMDs. Despite the promising data available, significant challenges remain in translating basic research findings into clinical practice, highlighting the need for further investigation into the complex pathophysiology underlying CMDs.

摘要

心脏代谢疾病(CMDs)是相互关联的多因素病症,包括动脉高血压、2型糖尿病、心力衰竭、冠状动脉疾病和中风。由于与CMDs患病率上升相关的心血管发病率和死亡率负担,在其管理中迫切需要新的诊断和治疗策略。在临床实践中,诸如心外膜脂肪组织评估、心室-动脉耦合和运动耐量研究等创新方法有助于阐明与CMDs相关的多方面机制。同样,涉及非编码RNA、染色质调节和细胞衰老的表观遗传变化可能代表CMDs的新型生物标志物和靶点。尽管有可用的有前景的数据,但将基础研究结果转化为临床实践仍面临重大挑战,这突出了对CMDs潜在复杂病理生理学进行进一步研究的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67c7/11122330/2a29a79fc02e/jcm-13-02883-g001.jpg

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