Novel Techniques, Biomarkers and Molecular Targets to Address Cardiometabolic Diseases

被引:0
|
作者
Di Fiore, Valerio [1 ]
Cappelli, Federica [1 ]
Del Punta, Lavinia [1 ]
De Biase, Nicolo [1 ]
Armenia, Silvia [1 ]
Maremmani, Davide [1 ]
Lomonaco, Tommaso [2 ]
Biagini, Denise [2 ]
Lenzi, Alessio [2 ]
Mazzola, Matteo [3 ]
Trico, Domenico [1 ]
Masi, Stefano [1 ]
Mengozzi, Alessandro [1 ]
Pugliese, Nicola Riccardo [1 ]
机构
[1] Univ Pisa, Dept Clin & Expt Med, Via Roma 67, I-56124 Pisa, Italy
[2] Univ Pisa, Dept Chem & Ind Chem, Via Giuseppe Moruzzi 13, I-56124 Pisa, Italy
[3] Univ Pisa, Dept Surg Med & Mol Pathol & Crit Care Med, Via Paradisa 2, I-56124 Pisa, Italy
关键词
cardiometabolic desease; arterial hypertension; type 2 diabetes mellitus; heart failure; novel markers; EPICARDIAL ADIPOSE-TISSUE; LONG NONCODING RNAS; HEART-FAILURE; NATRIURETIC-PEPTIDE; EJECTION FRACTION; SIRT1; RESVERATROL; ASSOCIATION; DYSFUNCTION; INFLAMMATION;
D O I
10.3390/jcm13102883
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
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页数:19
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