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Clinico-biological Collection of Subjects With Hyper Lipoprotein a in Reunion Island (COLLIPAR)

C

Centre Hospitalier Universitaire de la Réunion

Status

Enrolling

Conditions

Cardiovascular Disease

Treatments

Other: blood lipoprotein (a) test

Study type

Interventional

Funder types

Other

Identifiers

NCT04310917
2020/CHU/01

Details and patient eligibility

About

Cardiovascular disease (CVD) is the second leading cause of death in France and the leading cause of death on Reunion Island. Some modifiable risk factors for cardiovascular diseases are well identified and can be easily modulated, in particular by hygiene and dietetic measures (tobacco, sedentary lifestyle). Other risk factors such as high blood pressure, diabetes or dyslipidemia can also be pharmacologically modulated. On the other hand, there is a cardiovascular risk factor that we do not know how to modulate: a high level of lipoprotein (a) (Lp (a)), whose regulation remains largely unknown.

High plasma levels of Lipoprotein (a) remain a major risk for the development of cardiovascular disease and its clinical complications, which no drug can currently reduce. Understanding the biological and genetic determinants modulating Lp (a) levels remains a major challenge for treating subjects with hyper Lp (a). Several individuals and possibly Reunion families have been detected as having abnormally high rates of apo (a)

Thanks to the link between cardiovascular clinical picture, Lp (a) concentration and other biological markers, the study should allow a better understanding of the mechanisms underlying the cardiovascular risk in order to offer advice. prevention and care of at-risk subjects screened; or even avenues for adapted genetic counseling (DNA sequencing).

At the genetic level, several hypotheses could be explored making it possible to link the expression of the apo (a) protein to the genotype, in particular the presence of mutations in the gene, in the promoter region, polymorphisms, or epistatic regulation.

Enrollment

100 estimated patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patient with Lp (a)> 200 nmol / L OR member of family of a patient with Lp (a)> 200 nmol / L
  • be affiliated or beneficiary of a social security scheme
  • signed consent

Exclusion criteria

  • Refusal to participate

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

100 participants in 1 patient group

Lipoprotein a level
Other group
Description:
blood lipoprotein (a) test
Treatment:
Other: blood lipoprotein (a) test

Trial contacts and locations

1

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Central trial contact

Lucie AUZANNEAU

Data sourced from clinicaltrials.gov

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