Clinical Trial Details
— Status: Active, not recruiting
Administrative data
| NCT number |
NCT03373552 |
| Other study ID # |
FattoumaBourguiba |
| Secondary ID |
|
| Status |
Active, not recruiting |
| Phase |
|
| First received |
|
| Last updated |
|
| Start date |
August 12, 2015 |
| Est. completion date |
December 31, 2029 |
Study information
| Verified date |
September 2023 |
| Source |
Hôpital Universitaire Fattouma Bourguiba |
| Contact |
n/a |
| Is FDA regulated |
No |
| Health authority |
|
| Study type |
Observational [Patient Registry]
|
Clinical Trial Summary
The pathogenesis of CHD remains poorly known despite much research over the last few decades.
Numerous non-genetic variables have been demonstrated to have a significant impact on the
risk of CHD. However, the fact that many individuals with severe CHD do not have any of these
non-genetic risk factors supports the notion that genetic factors play a role in the
occurrence and progression of CHD. In this study, we investigated the association of
polymorphisms affecting Vascular endothelial factors A (VEGFA) and its receptor VEGFR2
(rs3025039, rs699947, rs2305948, rs1870377), CXCR4 (rs2228014), CCR2 (rs1799864), C3
(rs2230199), CCL2 (rs1024611 and rs2857656) and CCL5 (rs2107538 and rs22280789) with CHD
susceptibility and the severity of coronary lesion.
On another side, clopidogrel is largely prescribed in association with aspirin in order to
prevent atherothrombotic complications in patients with acute coronary syndrome. Its
effectiveness is undeniably proven by several studies and clinical trials over the years,
however, some patients have presented ischemic events such as thrombosis on stent or
myocardial infarction despite a well-conducted treatment. This clopidogrel non-responsiveness
is probably multifactorial; several genetic and non genetic factors may contribute to
impaired platelet inhibition by clopidogrel. In this regard, it is meaningful to determine
genetic polymorphisms contributing to the variability of clopidogrel response in patients
with Coronary Artery Therefore, the goal of this study is to determine the impact of the
polymorphisms, affecting CYP2C19, PON, ABCB1, ITGB3 and P2RY12 genes, on the response to
clopidogrel in patients with CAD.Disease (CAD). In fact, the recognition of these factors
might predict the exposure to the risk of thrombosis and cardiovascular death in these
patients.
Description:
The pathological basis of CHD is atherosclerosis and its clinical manifestations such as
ischemia. The formation of functional collateral circulation around obstructed arteries in
ischemic myocardial is an important process associated with improved survival in CHD
patients. Vascular endothelial factors A (VEGFA) and its receptor VEGFR2 have been cited as
crucial players in angiogenesis, the process of creating new blood vessels, and the control
of vasopermeability. They are essentially made by blood vessel endothelial and smooth muscle
cells. The VEGFA and VEGFR2 signaling pathway govern inflammation and modify the process of
thrombus formation in addition to their role in angiogenesis. Moreover, the atherosclerotic
process in human coronary arteries has been established in prior research to be accompanied
with higher serum levels of VEGF.
Consequently, atherosclerosis is considered now to be an inflammatory disease. Chemokines are
inflammatory chemotactic cytokines that play a role in leucocyte recruitment and the
chemokine CCL2 (monocyte chemoattractant protein-1 or MCP-1) has been found to be highly
expressed in human atherosclerotic plaques. CCL2 attracts monocytes as well as T lymphocytes
and mediates its effects by binding to G protein coupled receptors expressed on the surface
of target cells. The most prominent receptor for CCL2 is CCR2 and its binding to this
receptor has been shown to result in recruitment of monocytes into the subendothelial space.
Another chemokine that plays a critical role in development of CHD is CCL5 or RANTES
(regulation upon activation normal T cell expressed and secreted), which belongs to the CC
chemokines family and secreted from CD8+ T cells, epithelial cells, fibroblasts and
platelets. The CCL5-mediated cell migration is facilitated through its interaction with
chemokine receptors CCR1-3 and CCR5. Increased serum concentrations of CCL5 are associated
with obesity, type 2 diabetes (T2D), coronary atherosclerosis and other cardiovascular risk
factors including atherosclerosis.
Additionally, previous studies have shown that C3 is associated with atherosclerosis and
cardiovascular risk factors. Increased deposition of C3 within the intima of atherosclerotic
lesions suggests that complement may play a direct functional role in atherosclerosis.
Preclinical and clinical evidence suggested that complement C3 might be a biomarker of
insulin resistance and cardio-metabolic diseases. in CHD patients, serum C3 was significantly
higher than in controls, and was positively associated with the severity of CHD.
Clopidogrel, with or without aspirin, has been proven to reduce the occurrence of new stroke
in patients with acute ischemic stroke or transient ischemic attack. Previous studies showed
that genetic polymorphisms, especially those associated with reduced function of cytochrome
P450 2C19 (CYP2C19), were associated with excess cardiovascular risk and mortality in
patients with coronary artery disease treated with Clopidogrel. In Addition, Clopidogrel
binds to ADP receptor (P2Y12), and genetic polymorphisms in P2Y12 gene (H1 and H2) haplotypes
affect the phenotypic response to the drug.
Clopidogrel absorption is mainly limited by P-glycoprotein (P-gp) (2), encoded by ABCB1, an
ATP-dependent transporter located in the intestinal epithelial cell wall which expels the
drug into the intestinal lumen. mutations in ABCB1 appeared as a predictor of a better
response.
P2Y12 is the ADP receptor expressed on platelets surface and when clopidogrel irreversibly
binds to it makes impossible the bond of its natural ligand thus inhibiting platelets
aggregation. This receptor is highly polymorphic and many SNPs have been found to increase
the risk of CAD and hight platelet aggregation resulting in less clinical response to
clopidogrel.
Collected data for patients encompasse baseline characteristics, including age, gender,
obesity (defined as a body mass index ≥30 kg/m2), smoking, medical history, and
coadministered drugs.
The study protocol was approved by the Ethics Committee for Clinical Research at our center
and all subjects gave informed consent for study participation.
Platelet function assay is assessed by the VerifyNow P2Y12 analyzer following manufacturer
instructions (Accumetrics, Inc. San Diego, CA, USA) using venous blood samples collected in
tube containing 3.2% sodium citrate.
Genotyping is performed using the polymerase chain reaction-restriction fragment length
polymorphism (PCR-RFLP) and sequencing.
