American Journal of Cardiology
Volume 104, Issue 11 , Pages 1457-1464, 1 December 2009

Effects of Combination Lipid Therapy on Coronary Stenosis Progression and Clinical Cardiovascular Events in Coronary Disease Patients With Metabolic Syndrome: A Combined Analysis of the Familial Atherosclerosis Treatment Study (FATS), the HDL-Atherosclerosis Treatment Study (HATS), and the Armed Forces Regression Study (AFREGS)

  • Xue-Qiao Zhao, MD

      Affiliations

    • Department of Medicine, Division of Cardiology, University of Washington School of Medicine, Seattle, Washington
    • Corresponding Author InformationCorresponding author: Tel: 206-616-4905; fax: 206-616-4667
  • ,
  • Richard A. Krasuski, MD

      Affiliations

    • Department of Cardiology, Cleveland Clinic, Cleveland, Ohio
  • ,
  • Jefferson Baer, MD

      Affiliations

    • Department of Cardiology, Emory University, Atlanta, Georgia
  • ,
  • Edwin J. Whitney, MD

      Affiliations

    • Heart Vascular Institute of Texas, San Antonio, Texas
  • ,
  • Blazej Neradilek, MS

      Affiliations

    • Mountain-Whisper-Light Statistical Consulting, Seattle, Washington
  • ,
  • Alan Chait, MD

      Affiliations

    • Division of Metabolism, Endocrinology, and Nutrition, University of Washington School of Medicine, Seattle, Washington
  • ,
  • Santica Marcovina, PhD, ScD

      Affiliations

    • Division of Metabolism, Endocrinology, and Nutrition, University of Washington School of Medicine, Seattle, Washington
  • ,
  • John J. Albers, PhD

      Affiliations

    • Division of Metabolism, Endocrinology, and Nutrition, University of Washington School of Medicine, Seattle, Washington
  • ,
  • B. Greg Brown, MD, PhD

      Affiliations

    • Department of Medicine, Division of Cardiology, University of Washington School of Medicine, Seattle, Washington

Received 28 February 2009; received in revised form 2 July 2009; accepted 2 July 2009.

We examined the impact of metabolic syndrome (MS) on coronary stenosis progression and major cardiovascular (CV) events and investigated the mitigating effects of low-density lipoprotein (LDL) cholesterol lowering and LDL cholesterol lowering plus high-density lipoprotein (HDL) cholesterol increasing. This analysis combined individual patient data from 445 subjects who participated in 3 double-blinded, randomized, placebo-controlled trials (FATS, HATS, and AFREGS) comparing intensive lipid therapy to placebos on coronary stenosis progression by quantitative coronary angiography and on major CV events. The primary end points were change in mean proximal coronary diameter stenosis (Δ%Sprox) over 3 years and the frequency of the predefined composite of coronary artery disease death, nonfatal myocardial infarction, stroke, and revascularization due to worsening ischemia. Patients with MS had 50% more rapid coronary stenosis progression and 64% increased CV event frequency compared to those without. More rapid coronary stenosis progression was significantly and independently associated with a 3.5-fold increased event risk (p <0.001). Combination lipid therapy significantly decreased stenosis progression by 83% (Δ%Sprox 0.5 vs 2.9, p <0.001) in patients with MS and induced a small net regression in those without (Δ%Sprox −0.3 vs 2.0, p <0.001). Combination therapy decreased the event rate by 54% (13% vs 28%, p = 0.03) in those with MS and by 82% (3% vs 17%, p = 0.002) without. On average, each 10% decrease in LDL cholesterol or 10% increase in HDL cholesterol was significantly associated with a 0.3 Δ%Sprox decrease. Each 10% decrease in LDL cholesterol or 10% increase in HDL cholesterol was associated with 11% (p = 0.02) or 22% (p <0.001) event risk decrease. In conclusion, patients with MS have significantly more rapid coronary stenosis progression and a higher frequency of CV events. Greater stenosis progression rate is associated with a higher event rate. LDL cholesterol–lowering and HDL cholesterol–increasing therapies independently and significantly decrease coronary stenosis progression and decrease CV events.

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

 The Familial Atherosclerosis Treatment Study was supported by Grants P01 HL30086 and R01 HL19451 from the National Heart, Lung, and Blood Institute, Bethesda, Maryland. The HDL-Atherosclerosis Treatment Study was supported in part by Grant R01 HL49546 from the National Heart, Lung, and Blood Institute, Bethesda, Maryland and the 2 studies were supported with National Institutes of Health funding through the Clinical Nutrition Research Unit (DK 35816) and the Diabetes Endocrinology Research Center (DK 17047) at the University of Washington, Seattle, Washington. The Armed Forces Regression Study was supported by an unrestricted grant from the former Parke Davis Branch of Pfizer, Inc., New York, New York.

PII: S0002-9149(09)01353-8

doi:10.1016/j.amjcard.2009.07.035

American Journal of Cardiology
Volume 104, Issue 11 , Pages 1457-1464, 1 December 2009