Atherogenic dyslipidemia and residual cardiovascular risk in statin-treated patients

Gaia Sirimarco1, Julien Labreuche, Eric Bruckert

  • 1From the INSERM U698 and Paris-Diderot University, Sorbonne Paris Cité, Paris, France (G.S., J.L., P.A.); Department of Neurology and Stroke Centre, Bichat University Hospital, Paris, France (G.S., P.A.); Department of Biostatistics, EA2694, UDSL, University of Lille Nord de France, CHU Lille, Lille, France (J.L.); Department of Endocrinology, Pitié-Salpêtrière University Hospital, Paris, France (E.B.); Department of Neurology, Duke Comprehensive Stroke Center, Durham VAMC, Durham, NC (L.B.G.); NHLI Imperial College, ICMS, Royal Brompton Hospital, London, United Kingdom (K.M.F.); and Stroke Prevention Research Unit, NIHR Biomedical Research Centre, John Radcliffe Hospital, Oxford, United Kingdom (P.M.R.).

Stroke
|April 17, 2014
PubMed

Insights

Atherogenic dyslipidemia, characterized by low HDL cholesterol and high triglycerides, increases cardiovascular risk in patients on statin therapy. Further research is needed to develop targeted treatments for this residual risk.

Area of Science:

  • Cardiology
  • Clinical Research
  • Pharmacology

Background:

  • Statin therapy effectively reduces cardiovascular events but leaves residual risk.
  • Atherogenic dyslipidemia, defined by low high-density lipoprotein cholesterol (HDL-C) and high triglycerides (TG), contributes to this residual risk.
  • This study investigates the impact of atherogenic dyslipidemia on cardiovascular outcomes in patients treated with statins.

Purpose of the Study:

  • To assess the association between atherogenic dyslipidemia and residual cardiovascular risk in patients who experienced stroke or transient ischemic attack (TIA).
  • To evaluate the persistence of atherogenic dyslipidemia despite statin therapy.
  • To inform the development of novel therapeutic strategies targeting residual cardiovascular risk.

Main Methods:

  • Analysis of data from the PERFORM and SPARCL trials, including patients treated with statins.
  • Assessment of high-density lipoprotein cholesterol (HDL-C) and triglycerides (TG) levels 3 months post-randomization.
  • Primary outcome: major adverse cardiovascular events (MACE) including nonfatal myocardial infarction, nonfatal stroke, or cardiovascular death.
  • Utilized time-varying analysis to incorporate all available lipid measurements.

Main Results:

  • Approximately 10% of patients in PERFORM and 9% in SPARCL exhibited atherogenic dyslipidemia after initiating statin therapy.
  • Atherogenic dyslipidemia was associated with a significantly higher risk of major cardiovascular events in both trials (unadjusted HRs ~1.36-1.40).
  • The association remained significant after multivariable adjustment, although attenuated (adjusted HRs ~1.23-1.24).

Conclusions:

  • Atherogenic dyslipidemia is a significant contributor to residual cardiovascular risk in stroke/TIA patients receiving statin therapy.
  • The findings highlight the need for therapeutic interventions specifically targeting atherogenic dyslipidemia.
  • Further clinical trials are warranted to evaluate novel treatments for this high-risk population.
Abstract

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