Relevance of Plasma PCSK9 Concentration as a Biomarker in Acute Coronary Syndrome.

Last updated: September 13, 2021
Sponsor: Nantes University Hospital
Overall Status: Completed

Phase

N/A

Condition

Heart Disease

Chest Pain

Cardiac Disease

Treatment

N/A

Clinical Study ID

NCT01109706
BRD/10/03-ZE
  • Ages > 18
  • All Genders

Study Summary

PCSK9 (Proprotein convertase subtilisin kexin type 9) plays a key role in LDL-cholesterol (LDLC) metabolism by inhibiting LDL receptor (LDLR) at post-transcriptional level. PCSK9 loss of function mutations are associated to decreased LDLC levels and a cardiovascular protection. In this context, the development of pharmacological inhibitors of PCSK9, in association with statins treatment, represents a major therapeutic issue for LDLC modulation. It was previously shown that PCSK9 plasmatic concentration correlated with plasmatic LDLC, TG and glucose concentrations. However, no data are available on predictive value of PCSK9 plasmatic level concerning coronary disease severity.

The main objective of this study is to determine whether plasmatic PCSK9 concentration is linked to coronary damage severity in patients with acute coronary syndrome.

Eligibility Criteria

Inclusion

Inclusion criteria:

  • more than 18 years old
  • Acute coronary syndrome (ST+ or ST-)
  • 2 groups of patients: with statin, and without statin treatment

Exclusion

Exclusion criteria:

  • Patient who had cancer during the last 5 years or with cancer in progress
  • Patient with severe infection in progress
  • Hepatic failure (TP<50%)
  • Severe kidney failure
  • Patient unable to give his consent to the study

Study Design

Total Participants: 175
Study Start date:
February 13, 2011
Estimated Completion Date:
July 16, 2015

Connect with a study center

  • Nantes University Hospital

    Nantes, 44093
    France

    Site Not Available

  • Nantes University hospital

    Nantes, 44000
    France

    Site Not Available

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