HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Association of high-density lipoprotein particle concentration with cardiovascular risk following acute coronary syndrome: A case-cohort analysis of the dal-Outcomes trial.

AbstractBACKGROUND:
High-density lipoprotein cholesterol (HDL-C) concentration is inversely related to risk of major adverse cardiovascular events (MACE) in epidemiologic studies but is a poorer predictor of MACE in patients with established coronary heart disease. HDL particle concentration (HDLP) has been proposed as a better predictor of risk. We investigated whether HDLP is associated with risk of MACE after acute coronary syndrome (ACS).
METHODS:
The dal-Outcomes trial compared the CETP inhibitor dalcetrapib with placebo in patients with recent ACS. In a nested case-cohort analysis, total, large, medium, and small HDLPs were measured by nuclear magnetic resonance spectroscopy at baseline (4-12 weeks after ACS) in 476 cases with MACE and 902 controls. Hazard ratios (HRs; case-control) for 1-SD increment of HDLP or HDL-C at baseline were calculated with and without adjustment for demographic, clinical, laboratory, and treatment variables. Similarly, HRs for MACE were calculated for changes in HDLP or HDL-C from baseline to month 3 of assigned treatment.
RESULTS:
Over median follow-up of 28 months, the risk of MACE was not associated with baseline HDLP (adjusted HR = 0.98, 95% CI = 0.84-1.15, P = .81), any HDLP subclass, or HDL-C. Dalcetrapib increased HDL-C and total, medium, and large HDLP and decreased small HDLP but had no effect on MACE compared with placebo. There were no association of risk of MACE with change in HDLP or HDL-C and no interaction with assigned study treatment.
CONCLUSIONS:
Neither baseline HDLP nor the change in HDLP on treatment with dalcetrapib or placebo was associated with risk of MACE after ACS.
AuthorsTaufiq Salahuddin, John Kittelson, Jean-Claude Tardif, Prediman K Shah, Anders G Olsson, Stephen J Nicholls, Eran Leitersdorf, Lawrence A Leiter, David Kallend, Donald M Black, Philip J Barter, Christie M Ballantyne, Gregory G Schwartz
JournalAmerican heart journal (Am Heart J) Vol. 221 Pg. 60-66 (03 2020) ISSN: 1097-6744 [Electronic] United States
PMID31927126 (Publication Type: Journal Article)
CopyrightPublished by Elsevier Inc.
Chemical References
  • Amides
  • Anticholesteremic Agents
  • Cholesterol, HDL
  • Esters
  • Lipoproteins, HDL
  • Sulfhydryl Compounds
  • dalcetrapib
Topics
  • Acute Coronary Syndrome (blood, drug therapy)
  • Aged
  • Amides
  • Angina, Unstable (epidemiology)
  • Anticholesteremic Agents (therapeutic use)
  • Case-Control Studies
  • Cholesterol, HDL (blood)
  • Coronary Disease (mortality)
  • Esters
  • Female
  • Hospitalization (statistics & numerical data)
  • Humans
  • Lipoproteins, HDL (blood)
  • Magnetic Resonance Spectroscopy
  • Male
  • Middle Aged
  • Myocardial Infarction (epidemiology)
  • Prognosis
  • Randomized Controlled Trials as Topic
  • Stroke (epidemiology)
  • Sulfhydryl Compounds (therapeutic use)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: