Role of Matrix Metalloproteinase-2 in the Development of Atherosclerosis among Patients with Coronary Artery Disease.
Nazirah SamahAzizah UgusmanAdila A HamidNadiah S SulaimanAmilia AminuddinPublished in: Mediators of inflammation (2023)
Coronary artery disease (CAD) is a caused by atherosclerotic plaque buildup in the coronary arteries that supply blood and oxygen to the heart. Matrix metalloproteinase (MMP) is a family of zinc-dependent endopeptidase that is involved in various stages of atherosclerosis as demonstrated in in vitro and in vivo studies. MMP-2 is associated with both stable and unstable atherosclerotic plaque formation. The current review aimed to identify the role of MMP-2 in atherosclerosis development among CAD patients. Literature search was conducted through four online databases and only studies that were published from 2018 until February 2023 were included. The risk of bias was assessed by using the Newcastle-Ottawa Scale. A total of 10,622 articles were initially identified, and only eight studies that fulfilled the selection criteria were included in this review. The results showed that MMP-2 levels and activity were higher in patients with unstable CAD than those with stable CAD and healthy subjects. There was a significant association between MMP-2 levels and cardiovascular disease with MMP-14 levels, which is a pro-MMP-2 activator. In addition, two single nucleotide polymorphisms of the MMP-2 gene (rs243865 and rs243866) were significantly associated with the development of atherosclerosis. In conclusion, MMP-2 plays a crucial role in the development of atherosclerosis among patients with CAD and could be a potential target for CAD therapy.
Keyphrases
- coronary artery disease
- cardiovascular disease
- cell migration
- cardiovascular events
- percutaneous coronary intervention
- coronary artery bypass grafting
- type diabetes
- heart failure
- end stage renal disease
- chronic kidney disease
- healthcare
- stem cells
- newly diagnosed
- coronary artery
- risk assessment
- ejection fraction
- aortic stenosis
- randomized controlled trial
- toll like receptor
- mesenchymal stem cells
- genome wide
- dna methylation
- copy number
- atrial fibrillation
- transcatheter aortic valve replacement
- oxide nanoparticles