Immune-Mediated Inflammation in Vulnerable Atherosclerotic Plaques.
Harald ManggeGunter AlmerPublished in: Molecules (Basel, Switzerland) (2019)
Atherosclerosis is a chronic long-lasting vascular disease leading to myocardial infarction and stroke. Vulnerable atherosclerotic (AS) plaques are responsible for these life-threatening clinical endpoints. To more successfully work against atherosclerosis, improvements in early diagnosis and treatment of AS plaque lesions are required. Vulnerable AS plaques are frequently undetectable by conventional imaging because they are non-stenotic. Although blood biomarkers like lipids, C-reactive protein, interleukin-6, troponins, and natriuretic peptides are in pathological ranges, these markers are insufficient in detecting the critical perpetuation of AS anteceding endpoints. Thus, chances to treat the patient in a preventive way are wasted. It is now time to solve this dilemma because clear results indicate a benefit of anti-inflammatory therapy per se without modification of blood lipids (CANTOS Trial, NCT01327846). This fact identifies modulation of immune-mediated inflammation as a new promising point of action for the eradication of fatal atherosclerotic endpoints.
Keyphrases
- oxidative stress
- anti inflammatory
- cardiovascular disease
- atrial fibrillation
- heart failure
- high resolution
- coronary artery disease
- genome wide
- study protocol
- clinical trial
- fatty acid
- left ventricular
- case report
- randomized controlled trial
- type diabetes
- dna methylation
- gene expression
- stem cells
- phase ii
- mesenchymal stem cells
- brain injury
- bone marrow
- drug induced
- blood brain barrier
- cell therapy
- subarachnoid hemorrhage
- open label
- photodynamic therapy
- cerebral ischemia