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Function of High Density Lipoproteins in Acute Coronary Syndromes

High Density Lipoprotein Function in Acute Coronary Syndromes

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01278875
Acronym
HDL_ACS
Enrollment
65
Registered
2011-01-19
Start date
2011-01-31
Completion date
2025-12-31
Last updated
2023-10-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Coronary Syndrome

Keywords

High density lipoproteins, Acute coronary syndromes, Cellular cholesterol efflux, HDL: proteomics, Nitric Acid production

Brief summary

High density lipoproteins (HDL) have many effects that protect against cardiovascular diseases. In an acute heart attack (acute coronary syndrome -ACS), HDL change in composition and structure, reflecting the inflammatory environment that accompanies an ACS. The investigators will examine the function of HDL during an ACS and again when the patient has recovered.

Detailed description

High density lipoproteins (HDL) have pleiotropic effects associated with protection against atherosclerosis. These effects include cellular cholesterol efflux, anti-inflammatory and anti-oxidant effects, increase in nitric acid (NO) production from vascular endothelial cells and differentiation of endothelial progenitor cells for repair at sites of vascular injury. The measurement of the cholesterol mass within HDL (HDL-C) does not provide an adequate measure of HDL function. The investigators therefore propose to test and validate biomarkers of HDL function in patients with acute coronary syndromes (ACS). Hypothesis: HDL lose their cardiovascular protective functions in ACS. The investigators hypothesize that these changes are transient and partly normalize within 12 weeks. In this proposal, the investigators will examine the function of HDL in acute coronary syndromes (ACS) and 12 weeks later, in the recovery phase. Acute coronary syndromes are characterized by an acute inflammatory reaction, a marked decrease in HDL in plasma and a shift of the HDL proteome to an inflammatory phenotype.

Interventions

None listed

Sponsors

McGill University
CollaboratorOTHER
McGill University Health Centre/Research Institute of the McGill University Health Centre
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* Men and women 18-80 years of age * Acute Coronary Syndrome within 72 hours of presentation * Elevated tropinins (T or I)

Exclusion criteria

* Refusal to participate * Inability to return for a 12 week follow-up visit * Hemodynamic instability requiring vasopressor support, mechanical ventricular assist devices, the need for coronary artery bypass surgery * Lack of documented atherosclerotic CAD * Uncontrolled hypertension * Triglycerides≥5mmol/L * Severe obesity (BMI≥35) * Alcohol intake\>21 drinks/week * Presence of thyroid, hepatic, or renal disease * Autoimmune disease or any chronic or acute infectious or inflammatory illness

Design outcomes

Primary

MeasureTime frameDescription
HDL-mediated cellular cholesterol efflux12 weeksBiomarkers of HDL function

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026