Role of Tryptase Levels in Patients With Stable Coronary Artery Disease. (TRY-CAD)

University of Thessaly

Status: Enrolling

Conditions: Chronic Coronary Syndrome

Study type: Observational

Funder types: Other

Identifiers

NCT06958016

447

Details and patient eligibility

About

The aim of this study is to measure the levels of serum tryptase and correlate them with the severity of coronary artery disease in study population. In addition, it will evaluate the usability of tryptase levels as a prognostic biomarker for future cardiovascular events.

Full description

Coronary artery disease (CAD) is the leading cause of death worldwide based on WHO' s latest review in 2019 with CAD being responsible for the 16% of them. The main feature of coronary artery disease is the accumulation of atherosclerotic plaque in the epicardial arteries whether obstructive or non-obstructive. CAD is further subclassified into Chronic Coronary Syndrome (CCS) and Acute Coronary Syndrome (ACS). Patients with CCS experience long and stable periods of myocardial ischemia. However, in the case of a plaque rapture these patients can turn into ACS patients. The objective of this study is to predict that sudden shifting of patients from CCS to ACS by associating the role of inflammation and its factors with cardiovascular events. In particular, it focuses on mast cell (MC) tryptase which provokes plaque instability in patients with CCS. Mast cells needs to be activated to release tryptase and their activation mechanism seems to be the bridging point between tryptase and coronary artery disease. Previous studies have shown that IgE levels, which is the most potent activator of MC, are found high in hyperlipidemic patients. In addition, oxidized LDL (Ox-LDL) is another MC activator.

In reference to the fact that there might be a correlation between tryptase and coronary plaque instability in patients with chronic coronary syndrome, the investigator propose an interventional study for the role of tryptase as a prognostic biomarker in patients with CCS by studying a large population of Greek subjects with CCS.

The study will be conducted on 2 patient population:

1. Patients without coronary artery disease (estimated stenosis <70%) - Control group
2. Patients with coronary artery disease (estimated stenosis >70%) - CAD group

Enrollment: 200 estimated patients

Sex: All

Ages: 18 to 85 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Male and female subjects aged 18 - 85 years old.
• Clinical symptoms of angina which are classified based on the Canadian Cardiovascular Score (CCS score)
• Positive SPECT scan for myocardial ischemia

Exclusion criteria

• Acute Coronary Syndrome 4 weeks before the coronary catheterization
• Percutaneous Coronary Angioplasty
• Coronary Artery Bypass Graft
• Active symptoms of allergy (asthma, urticaria)
• Mastocytosis
• Hypereosinophilia
• Autoimmune disease
• Cancer
• Kidney failure
• Myelodysplastic Syndrome
• Denial of signing informed consent

Trial design

200 participants in 2 patient groups

Coronary Artery Disease Group

Description:

Patients with angiographically proven coronary artery stenosis \>70%

Non-coronary Artery Disease Group

Description:

Patients with angiographically proven coronary artery stenosis \<70%