Matrix Metalloproteinases in Cardioembolic Stroke: From Background to Complications.
Anna WysockaJacek SzczygielskiMarta KopańskaJoachim M OertelAndrzej GlowniakPublished in: International journal of molecular sciences (2023)
Matrix metalloproteinases (MMPs) are endopeptidases participating in physiological processes of the brain, maintaining the blood-brain barrier integrity and playing a critical role in cerebral ischemia. In the acute phase of stroke activity, the expression of MMPs increase and is associated with adverse effects, but in the post-stroke phase, MMPs contribute to the process of healing by remodeling tissue lesions. The imbalance between MMPs and their inhibitors results in excessive fibrosis associated with the enhanced risk of atrial fibrillation (AF), which is the main cause of cardioembolic strokes. MMPs activity disturbances were observed in the development of hypertension, diabetes, heart failure and vascular disease enclosed in CHA 2 DS 2 VASc score, the scale commonly used to evaluate the risk of thromboembolic complications risk in AF patients. MMPs involved in hemorrhagic complications of stroke and activated by reperfusion therapy may also worsen the stroke outcome. In the present review, we briefly summarize the role of MMPs in the ischemic stroke with particular consideration of the cardioembolic stroke and its complications. Moreover, we discuss the genetic background, regulation pathways, clinical risk factors and impact of MMPs on the clinical outcome.
Keyphrases
- atrial fibrillation
- cerebral ischemia
- heart failure
- risk factors
- catheter ablation
- oral anticoagulants
- left atrial
- left atrial appendage
- direct oral anticoagulants
- subarachnoid hemorrhage
- brain injury
- percutaneous coronary intervention
- end stage renal disease
- ejection fraction
- chronic kidney disease
- blood pressure
- cardiovascular disease
- poor prognosis
- acute myocardial infarction
- coronary artery disease
- newly diagnosed
- body mass index
- patient reported outcomes
- adipose tissue
- replacement therapy
- insulin resistance