Baseline blood pressure, low- and high-density lipoproteins, and triglycerides and the risk of vascular events in the Stroke Prevention by Aggressive Reduction in Cholesterol Levels (SPARCL) trial

Pierre Amarenco, Larry B. Goldstein, Alfred Callahan, Henrik Sillesen, Michael G. Hennerici, Blair J. O'Neill, Amy E. Rudolph, Lisa Simunovic, Justin A. Zivin, K. M.A. Welch

Research output: Contribution to journalArticlepeer-review

87 Scopus citations

Abstract

Objective: To explore the relative contributions of baseline systolic blood pressure (SBP) and diastolic blood pressure (DBP) and lipoproteins on the risk of recurrent stroke or first major cardiovascular event (MCVE) and their potential impact on the benefit of statin treatment. Methods and results: The SPARCL trial randomized 4731 patients with recent stroke or transient ischemic attack (TIA) and no known coronary heart disease and LDL-C between 100 and 190 mg/dL to either atorvastatin 80 mg/d or placebo. Baseline assessment included SBP, DBP and measurements of low-density lipoprotein cholesterol (LDL-C) and high-density lipoprotein cholesterol (HDL-C), and triglyceride levels. After 4.9 years of follow-up, there were 575 primary end points (fatal and nonfatal stroke), including 491 ischemic strokes, and 740 MCVEs (stroke plus myocardial infarction and vascular death). Cox regression models analysis showed a trend (P > 0.05 and P < 0.10) for higher SBP but not DBP to be associated with an outcome stroke with only SBP associated with MCVE. Only baseline low HDL-C was associated with an outcome stroke. Baseline HDL-C, triglycerides, and LDL/HDL ratio were each associated with MCVEs. There were no interactions between any of these baseline variables and the effect of treatment on outcome strokes. Conclusions: In patients with recent stroke or TIA and no coronary heart disease, only lower baseline HDL-C predicted the risk of recurrent stroke with HDL-C, triglycerides, and LDL/HDL ratio associated with MCVE. Atorvastatin treatment was similarly effective regardless of baseline lipoprotein levels.

Original languageEnglish
Pages (from-to)515-520
Number of pages6
JournalAtherosclerosis
Volume204
Issue number2
DOIs
StatePublished - Jun 2009

Bibliographical note

Funding Information:
No content development support was provided, but assistance in preparing the figures and formatting the manuscript for submission was provided by Envision Pharma and funded by Pfizer Inc.

Funding Information:
Sources of funding: This study was sponsored by Pfizer Inc. Employees of Pfizer (the study sponsor) contributed to the design and conduct of the study, the collection, management, analysis, and interpretation of the data, and review of the manuscript.

Funding

No content development support was provided, but assistance in preparing the figures and formatting the manuscript for submission was provided by Envision Pharma and funded by Pfizer Inc. Sources of funding: This study was sponsored by Pfizer Inc. Employees of Pfizer (the study sponsor) contributed to the design and conduct of the study, the collection, management, analysis, and interpretation of the data, and review of the manuscript.

FundersFunder number
Envision Pharma
Pfizer

    Keywords

    • HDL-C
    • LDL-C
    • Statin
    • Stroke
    • TIA

    ASJC Scopus subject areas

    • Cardiology and Cardiovascular Medicine

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