Whole Genome Sequencing
GeneticWhole Genome Sequencing Biomarkers analyses
Other names: Biological analyzes
NCT Number: NCT03234127
The main objective of SAFIR is to identify the atherosclerotic genetic factors in these patients, which will identify new therapeutic targets for the treatment of CV and Familial Hypercholesterolemia diseases. In addition, SAFIR will allow the identification of new CV protection biomarkers, which will be useful tools for the development of a personalized medicine for the management of dyslipidemias.
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Notify Me40 year and older
All sexes
Interventional
Not applicable
Le Bocage Hospital, Dijon, France
The objective of the SAFIR study is to perform non-invasive coronary vascular phenotyping of familial hypercholesterolemia (FH) families by performing a coronary calcium score and then to detect protective genetic factors in patients who do not have a significant atheroma despite a perturbed biological phenotype.
The investigators will also conduct biochemical, lipidemic and metabolomic analyzes to identify a signature of biomarkers protective of cardiovascular risk in FH patients.
The investigators will use the French FH register, which already includes 3889 patients, to identify these "protected" FH families within the main reference centers for the management of FH for inclusion and follow-up of patients.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
The inclusion criteria to be met in the population with known coronary atheroma:
Inclusion criteria
to be met in the population without cardiovascular risk:
Inclusion criteria
to be met in the related population with familial hypercholesterolemia :
Inclusion criteria
to be met in the related population without familial hypercholesterolemia :
Exclusion criteria
The exclusion criterion for all populations except the related population without familial hypercholesterolemia:
Whole Genome Sequencing Biomarkers analyses
Other names: Biological analyzes
Time frame: 3 years
Identification of functional genetic variants by a Whole Genome Sequencing (WGS) approach in case-control analysis (FH without and with advanced coronary atherosclerosis) and/or family analysis (protected and affected relatives)
Time frame: 3 years
Lipidic panel, phosphocalcic panel, Ceramides, Alipoproteins, Lp(a), lipidomic, LDL size, Phospholipids, TMAO, Carnitin, Cholin, microbiota, metabolomic, LDL Ox, Sterols, Isoprostan, oxidation, inflammation, cytokins, oxidative stress.
Time frame: 3 years
Measurement of arterial stiffness measured by popmeter® (pulse wave velocity)
Time frame: 3 years
Measurement of ASD through arterial Doppler ultrasonography (Intra-media thickness (IMT), degree of stenosis (ESCT), plaque)
Time frame: 3 years
Measurement of lower extremity involvement by arterial doppler ultrasonography
Time frame: 3 years
Measurement of coronary calcium score and aortic valvular score (optional) by a thoracic CT scan
Time frame: 3 years
Measurement of coronary calcium score and aortic valvular score (optional) by a thoracic CT scan
Nantes University Hospital
Other
Acronym: SAFIR
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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