Assessment of GARP Expression in Acute and Chronic Coronary Syndrome

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversité Catholique de Louvain

About this trial

The leading cause of death is cardiovascular diseases in occidental countries. Of those, atherosclerosis is the major contributor to this burden being notably responsible for strokes and myocardial infarctions. The genesis of atherosclerosis is linked to both lipid accumulation and inflammation in the vascular wall of major arteries. One of the major pathways of inflammation is the TGF-beta axis which is at least partially regulated by the GARP protein. It has been investigated mostly in cancer biology but data in cardiovascular disease is lacking. Thus, the investigators aim to characterize the contribution of this protein by investigating its expression in circulating blood cells from patients with an acute or chronic coronary syndrom. The main cells expressing the GARP protein are the platelets and the T regulating cells which will be the main focus.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Older than 18 years

Able to give informed consent

Undergoing coronary angiography.

Disqualifiers

Patients younger than 18 years

Unable to give consent

Pregnancy

Dialysis

Trial design

Design model

Parallel

Treatments tested in this trial

  • Arterial blood sample

    Biological/Vaccine

    An arterial blood sample will be obtained at the beginning of the coronary angiography by using the arterial sheat in place.

Treatment groups

600 Participants
are divided into 3 treatment groups
Group A: Acute coronary syndromeExperimental treatment 1 intervention
Group B: Chronic coronary syndromeExperimental treatment 1 intervention
Group C: ControlExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Platelet GARP expression

The platelet GARP expression profile will be assessed and compared between arms using flow cytometry.

Time frame
Throughout the entire study, approximately during 2 years

Secondary outcomes

1

Inflammatory profile

The inflammatory cytokines (IL-1, IL-6, TNF,...) profile will be determined by multiplex and compared between arms.

Time frame
Throughout the entire study, approximately during 2 years

Other outcomes

Sponsors and contacts

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Université Catholique de Louvain

Lead sponsor

Fonds National de la Recherche Scientifique

Collaborator

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