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)

被引:41
作者
Zhao, Xue-Qiao [1 ]
Krasuski, Richard A. [4 ]
Baer, Jefferson [5 ]
Whitney, Edwin J. [6 ]
Neradilek, Blazej [3 ]
Chait, Alan [2 ]
Marcovina, Santica [2 ]
Albers, John J. [2 ]
Brown, B. Greg [1 ]
机构
[1] Univ Washington, Sch Med, Dept Med, Div Cardiol, Seattle, WA 98195 USA
[2] Univ Washington, Sch Med, Dept Med, Div Metab Endocrinol & Nutr, Seattle, WA 98195 USA
[3] Mt Whisper Light Stat Consulting, Seattle, WA USA
[4] Cleveland Clin, Dept Cardiol, Cleveland, OH 44106 USA
[5] Emory Univ, Dept Cardiol, Atlanta, GA 30322 USA
[6] Heart Vasc Inst Texas, San Antonio, TX USA
基金
美国国家卫生研究院;
关键词
DENSITY-LIPOPROTEIN CHOLESTEROL; INSULIN-RESISTANCE; HEART-DISEASE; DRUG PROJECT; PREVENTION; NIACIN; MORTALITY; TRIALS;
D O I
10.1016/j.amjcard.2009.07.035
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 (Delta%S-prox) 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% (Delta%S-prox 0.5 vs 2.9, p<0.001) in patients with MS and induced a small net regression in those without (Delta%S-prox -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 Delta%S-prox 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. (C) 2009 Elsevier Inc. All rights reserved. (Am J Cardiol 2009;104:1457-1464)
引用
收藏
页码:1457 / 1464
页数:8
相关论文
共 23 条
  • [1] [Anonymous], 2001, JAMA, V285, P2486
  • [2] BRESLOW NE, 1980, STAT METHODS CANC RE, V1, P29
  • [3] Simultaneous low-density lipoprotein-C lowering and high-density lipoprotein-C elevation for optimum cardiovascular disease prevention with various drug classes, and their combinations: a meta-analysis of 23 randomized lipid trials
    Brown, B. Greg
    Stukovsky, Karen Hinckley
    Zhao, Xue-Qiao
    [J]. CURRENT OPINION IN LIPIDOLOGY, 2006, 17 (06) : 631 - 636
  • [4] Simvastatin and niacin, antioxidant vitamins, or the combination for the prevention of coronary disease
    Brown, BG
    Zhao, XQ
    Chait, A
    Fisher, LD
    Cheung, MC
    Morse, JS
    Dowdy, AA
    Marino, EK
    Bolson, EL
    Alaupovic, P
    Frohlich, J
    Albers, JJ
    Serafini, L
    Huss-Frechette, E
    Wang, S
    DeAngelis, D
    Dodek, A
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2001, 345 (22) : 1583 - 1592
  • [5] BROWN BG, 1990, NEW ENGL J MED, V323, P1289
  • [6] CHANGES IN SEQUENTIAL CORONARY ARTERIOGRAMS AND SUBSEQUENT CORONARY EVENTS
    BUCHWALD, H
    MATTS, JP
    FITCH, LL
    CAMPOS, CT
    SANMARCO, ME
    AMPLATZ, K
    CASTANEDAZUNIGA, WR
    HUNTER, DW
    PEARCE, MB
    BISSETT, JK
    EDMISTON, WA
    SAWIN, HS
    WEBER, FJ
    VARCO, RL
    CAMPBELL, GS
    YELLIN, AE
    SMINK, RD
    LONG, JM
    HANSEN, BJ
    CHALMERS, TC
    MEIER, P
    STAMLER, J
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1992, 268 (11): : 1429 - 1433
  • [7] Benefits of niacin in patients with versus without the metabolic syndrome and healed myocardial infarction (from the Coronary Drug Project)
    Canner, PL
    Furberg, CD
    McGovern, ME
    [J]. AMERICAN JOURNAL OF CARDIOLOGY, 2006, 97 (04) : 477 - 479
  • [9] DAVIES MJ, 1993, BRIT HEART J, V69, P377
  • [10] FRIEDMAN LM, 1998, FUNDAMENTALS CLIN TR, P301