Statins, high-density lipoprotein cholesterol, and regression of coronary atherosclerosis

被引:543
|
作者
Nicholls, Stephen J.
Tuzcu, E. Murat
Sipahi, Ilke
Grasso, Adam W.
Schoenhagen, Paul
Hu, Tingfei
Wolski, Kathy
Crowe, Tim
Desai, Milind Y.
Hazen, Stanley L.
Kapadia, Samir R.
Nissen, Steven E.
机构
[1] Cleveland Clin, Dept Cardiovasc Med, Cleveland, OH 44195 USA
[2] Cleveland Clin, Dept Cell Biol, Cleveland, OH 44195 USA
[3] Cleveland Clin, Dept Diagnost Radiol, Cleveland, OH 44195 USA
[4] Cleveland Clin, Ctr Cardiovasc Diagnost & Prevent, Cleveland, OH 44195 USA
来源
关键词
D O I
10.1001/jama.297.5.499
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context Statins reduce low-density lipoprotein cholesterol (LDL-C) levels and slow progression of coronary atherosclerosis. However, no data exist describing the relationship between statin-induced changes in high-density lipoprotein cholesterol (HDL-C) and disease progression. Objective To investigate the relationship between changes in LDL-C and HDL-C levels and atheroma burden. Design, Setting, and Patients Post-hoc analysis combining raw data from 4 prospective randomized trials ( performed in the United States, North America, Europe, and Australia between 1999 and 2005), in which 1455 patients with angiographic coronary disease underwent serial intravascular ultrasonography while receiving statin treatment for 18 months or for 24 months. Ultrasound analysis was performed in the same core laboratory for all of the studies. Main Outcome Measure Relationship between changes in lipoprotein levels and coronary artery atheroma volume. Results During statin therapy, mean (SD) LDL-C levels were reduced from 124.0 (38.3) mg/dL (3.2 [0.99] mmol/L) to 87.5 (28.8) mg/dL (2.3 [0.75] mmol/L) (a 23.5% decrease; P <. 001), and HDL-C levels increased from 42.5 (11.0) mg/dL(1.1 [0.28] mmol/L) to 45.1 (11.4) mg/dL(1.2 [0.29] mmol/L)(a 7.5% increase; P <. 001). The ratio of LDL-C to HDL-C was reduced from a mean ( SD) of 3.0 ( 1.1) to 2.1 (0.9) (a 26.7% decrease; P <. 001). These changes were accompanied by a mean ( SD) increase in percent atheroma volume from 39.7% (9.8%) to 40.1% (9.7%) ( a 0.5% [3.9%] increase; P=. 001) and a mean ( SD) decrease in total atheroma volume of 2.4 (23.6) mm(3) ( P <. 001). In univariate analysis, mean levels and treatment-mediated changes in LDL-C, total cholesterol, non-HDL cholesterol, apolipoprotein B, and ratio of apolipoprotein B to apolipoprotein A-I were significantly correlated with the rate of atherosclerotic progression, whereas treatment-mediated changes in HDL-C were inversely correlated with atheroma progression. In multivariate analysis, mean levels of LDL-C ( beta coefficient, 0.11 [95% confidence interval, 0.07-0.15]) and increases in HDL-C( beta coefficient,- 0.26[ 95% confidence interval,- 0.41 to - 0.10]) remained independent predictors of atheroma regression. Substantial atheroma regression ( >= 5% reduction in atheroma volume) was observed in patients with levels of LDL-C less than the mean( 87.5 mg/dL) during treatment and percentage increases of HDL-C greater than the mean( 7.5%; P <. 001). No significant differences were found with regard to clinical events. Conclusions Statin therapy is associated with regression of coronary atherosclerosis when LDL-C is substantially reduced and HDL-C is increased by more than 7.5%. These findings suggest that statin benefits are derived from both reductions in atherogenic lipoprotein levels and increases in HDL-C, although it remains to be determined whether the atherosclerotic regression associated with these changes in lipid levels will translate to meaningful reductions in clinical events and improved clinical outcomes.
引用
收藏
页码:499 / 508
页数:10
相关论文
共 50 条
  • [1] High-density lipoprotein cholesterol and the role of statins
    Chong, PH
    Kezele, R
    Franklin, C
    [J]. CIRCULATION JOURNAL, 2002, 66 (11) : 1037 - 1044
  • [2] Therapies to increase high-density lipoprotein cholesterol and their effect on cardiovascular outcomes and regression of atherosclerosis
    Venkatesh, Prasanna K.
    Caskey, David
    Reddy, Pratap C.
    [J]. AMERICAN JOURNAL OF THE MEDICAL SCIENCES, 2008, 336 (01): : 64 - 68
  • [3] High-Density Lipoprotein, Lecithin: Cholesterol Acyltransferase, and Atherosclerosis
    Ossoli, Alice
    Pavanello, Chiara
    Calabresi, Laura
    [J]. ENDOCRINOLOGY AND METABOLISM, 2016, 31 (02) : 223 - 229
  • [4] Atherosclerosis regression: Is low-density lipoprotein or high-density lipoprotein the answer?
    Nicholls S.J.
    Tuzcu E.M.
    Nissen S.E.
    [J]. Current Atherosclerosis Reports, 2007, 9 (4) : 266 - 273
  • [5] Effects on Coronary Atherosclerosis by Targeting Low-Density Lipoprotein Cholesterol with Statins
    Jean Ferrières
    [J]. American Journal of Cardiovascular Drugs, 2009, 9 : 109 - 115
  • [6] Effects on Coronary Atherosclerosis by Targeting Low-Density Lipoprotein Cholesterol with Statins
    Ferrieres, Jean
    [J]. AMERICAN JOURNAL OF CARDIOVASCULAR DRUGS, 2009, 9 (02) : 109 - 115
  • [7] Association of the Low-Density Lipoprotein Cholesterol/High-Density Lipoprotein Cholesterol Ratio and Body Mass Index with Coronary Plaque Regression
    Tani, Shigemasa
    Matsumoto, Michiaki
    Nakamura, Yasutaka
    Nagao, Ken
    Hirayama, Atsushi
    [J]. AMERICAN JOURNAL OF CARDIOVASCULAR DRUGS, 2012, 12 (04) : 279 - 286
  • [8] Association of the Low-Density Lipoprotein Cholesterol/High-Density Lipoprotein Cholesterol Ratio and Body Mass Index with Coronary Plaque Regression
    Shigemasa Tani
    Michiaki Matsumoto
    Yasutaka Nakamura
    Ken Nagao
    Atsushi Hirayama
    [J]. American Journal of Cardiovascular Drugs, 2012, 12 (4) : 279 - 286
  • [9] Statins, high-density lipoprotein, and the low-density lipoprotein/high-density lipoprotein ratio
    Silva, JM
    [J]. AMERICAN JOURNAL OF CARDIOLOGY, 2000, 86 (05): : 593 - 594
  • [10] Cholesterol Efflux Capacity, High-Density Lipoprotein Function, and Atherosclerosis
    Khera, Amit V.
    Cuchel, Marina
    de la Llera-Moya, Margarita
    Rodrigues, Amrith
    Burke, Megan F.
    Jafri, Kashif
    French, Benjamin C.
    Phillips, Julie A.
    Mucksavage, Megan L.
    Wilensky, Robert L.
    Mohler, Emile R.
    Rothblat, George H.
    Rader, Daniel J.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2011, 364 (02): : 127 - 135