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Published on: November 10, 2017
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.).
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.
Background And Purpose:
Treatment with statins reduces the rate of cardiovascular events in high-risk patients, but residual risk persists. At least part of that risk may be attributable to atherogenic dyslipidemia characterized by low high-density lipoprotein cholesterol (≤40 mg/dL) and high triglycerides (triglycerides≥150 mg/dL).
Methods:
We studied subjects with stroke or transient ischemic attack in the Prevention of Cerebrovascular and Cardiovascular Events of Ischemic Origin With Terutroban in Patients With a History of Ischemic Stroke or Transient Ischemic Attack (PERFORM; n=19,100) and Stroke Prevention by Aggressive Reduction in Cholesterol Levels (SPARCL; n=4731) trials who were treated with a statin and who had high-density lipoprotein cholesterol and triglycerides measurements 3 months after randomization (n=10,498 and 2900, respectively). The primary outcome measure for this exploratory analysis was the occurrence of major cardiovascular events (nonfatal myocardial infarction, nonfatal stroke, or cardiovascular death). We also performed a time-varying analysis to account for all available high-density lipoprotein cholesterol and triglyceride measurements.
Results:
A total of 10% of subjects in PERFORM and 9% in SPARCL had atherogenic dyslipidemia after ≥3 months on start statin therapy. After a follow-up of 2.3 years (PERFORM) and 4.9 years (SPARCL), a major cardiovascular event occurred in 1123 and 485 patients in the 2 trials, respectively. The risk of major cardiovascular events was higher in subjects with versus those without atherogenic dyslipidemia in both PERFORM (hazard ratio, 1.36; 95% confidence interval, 1.14-1.63) and SPARCL (hazard ratio, 1.40; 95% confidence interval, 1.06-1.85). The association was attenuated after multivariable adjustment (hazard ratio, 1.23; 95% confidence interval, 1.03-1.48 in PERFORM and hazard ratio, 1.24; 95% confidence interval, 0.93-1.65 in SPARCL). Time-varying analysis confirmed these findings.
Conclusions:
The presence of atherogenic dyslipidemia was associated with higher residual cardiovascular risk in PERFORM and SPARCL subjects with stroke or transient ischemic attack receiving statin therapy. Specific therapeutic interventions should now be trialed to address this residual risk.
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