Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
150 participants
INTERVENTIONAL
2021-09-20
2026-06-19
Brief Summary
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Adenosine via A2A receptors (A2AR) plays a crucial role in the regulation of the cardiovascular and immune systems.
In this project, the investigators wish :
* To study whether the expression and function of A2AR in PBMCs are altered in human hypercholesterolemia, using as a study model a larger cohort of patients with hypercholesterolemia of increasing level and severity: polygenic form, heterozygous genetic form and homozygous genetic form in comparison with healthy subjects with normal cholesterol levels.
* To study whether A2AR expression and function in PBMCs are associated with blood levels of LDL-C and homocysteine and with the inflammatory status of patients.
* To assess whether the cholesterol-lowering therapies currently used to reduce LDL-C levels and thus the risk of CVD in hypercholesterolemic patients have an impact on possible alterations of A2AR expression and function in PBMCs.
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
DIAGNOSTIC
NONE
Study Groups
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Healthy volunteers
volunteers showing no hypercholesterolemia
Blood sample
Blood sampling.
Patients with untreated hypercholesterolemia at the time of inclusion
patients presenting hypercholesterolemia with no treatment at the time of inclusion
Blood sample
Blood sampling.
Patients with treated hypercholesterolemia at the time of inclusion
patients presenting hypercholesterolemia and treated at the time of inclusion
Blood sample
Blood sampling.
Interventions
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Blood sample
Blood sampling.
Eligibility Criteria
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Inclusion Criteria
* For the group of hypercholesterolemic patients :
* LDL-cholesterol level \>1.9 g/L with or without treatment to make the diagnosis of hypercholesterolemia (laboratory test less than 12 months old at inclusion)
* For the healthy group :
● No cholesterol-modifying therapy.
* Subject not having hypercholesterolemia (biological assessment less than 12 months old at inclusion with LDL-cholesterol level \< 1.9 g/L) and not taking cholesterol-lowering treatment.
* Subjects who are affiliated or beneficiaries of a social security plan
* Subject agreeing to participate in the study and having signed an informed consent
Exclusion Criteria
* Person who does not understand the French language
18 Years
80 Years
ALL
Yes
Sponsors
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Assistance Publique Hopitaux De Marseille
OTHER
Responsible Party
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Principal Investigators
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François CREMIEUX
Role: STUDY_DIRECTOR
AP-HM
Locations
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Service Endocrinologie
Marseille, , France
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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ID-RCB
Identifier Type: OTHER
Identifier Source: secondary_id
2021-07
Identifier Type: -
Identifier Source: org_study_id
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