Effect of pravastatin on coronary disease events in subgroups defined by coronary risk factors - The prospective pravastatin pooling project

被引:287
作者
Sacks, FM
Tonkin, AM
Shepherd, J
Braunwald, E
Cobbe, S
Hawkins, CM
Keech, A
Packard, C
Simes, J
Byington, R
Furberg, CD
机构
[1] Harvard Univ, Sch Publ Hlth, Dept Nutr, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Boston, MA 02115 USA
[3] Brigham & Womens Hosp, Boston, MA 02115 USA
[4] Natl Heart Fdn Australia, Melbourne, Vic, Australia
[5] Univ Glasgow, Glasgow, Lanark, Scotland
[6] Univ Texas, Sch Publ Hlth, Houston, TX USA
[7] Univ Sydney, Sydney, NSW 2006, Australia
[8] Wake Forest Univ, Winston Salem, NC 27109 USA
关键词
coronary disease; drugs; lipids; lipoproteins; meta-analysis;
D O I
10.1161/01.CIR.102.16.1893
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-Previous trials have had insufficient numbers of coronary events to address definitively the effect of lipid-modifying therapy on coronary heart disease in subgroups of patients with varying baseline characteristics. Methods and Results-The data from 3 large randomized trials with pravastatin 40 mg were pooled and analyzed with the use of a prospectively defined protocol. Included were 19 768 patients, 102 559 person-years of follow-up, 2194 primary end points (coronary death or nonfatal myocardial infarction), and 3717 expanded end points (primary end point, CABG, or PTCA). Pravastatin significantly reduced relative risk in younger (<65 years) and older (greater than or equal to 65 years) patients, men and women, smokers and nonsmokers, and patients with or without diabetes or hypertension. The relative effect was smaller, but absolute risk reduction was similar in patients with hypertension compared with those without hypertension. Relative risk reduction was significant in predefined categories of baseline lipid concentrations. Tests for interaction were not significant between relative risk reduction and baseline total cholesterol (5% to 95% range 177 to 297 mg/dL, 4.6 to 7.7 mmol/L), HDL cholesterol (27 to 58 mg/dL, 0.7 to 1.5 mmol/L), and triglyceride (74 to 302 mg/dL, 0.8 to 3.4 mmol/L) concentrations, analyzed as continuous variables. However, for LDL cholesterol, the probability values for interaction were 0.068 for the prespecified primary end point and 0.019 for the expanded end point. Relative risk reduction was similar throughout most of the baseline LDL cholesterol range (125 to 212 mg/dL, 3.2 to 5.5 mmol/L) with the possible exception of the lowest quintile of CARE/LIPID (<125 mg/dL) (relative risk reduction 5%, 95% CI 19% to -12%). Conclusions-Pravastatin treatment is effective in reducing coronary heart disease events in patients with high or low risk factor status and across a wide range of pretreatment lipid concentrations.
引用
收藏
页码:1893 / 1900
页数:8
相关论文
共 14 条
  • [1] CARLSON LA, 1988, ACTA MED SCAND, V223, P405
  • [2] FURBERG C, 1995, AM J CARDIOL, V76, P899
  • [3] Relation between baseline and on-treatment lipid parameters and first acute major coronary events in the Air Force/Texas Coronary Atherosclerosis Prevention Study (AFCAPS/TexCAPS)
    Gotto, AM
    Whitney, E
    Stein, EA
    Shapiro, DR
    Clearfield, M
    Weis, S
    Jou, JY
    Langendörfer, A
    Beere, A
    Watson, DJ
    Downs, JR
    de Cani, JS
    [J]. CIRCULATION, 2000, 101 (05) : 477 - 484
  • [4] GRAVES EJ, 1991, VITAL HLTH STAT, V13, P108
  • [5] McCullagh P., 2019, Generalized Linear Models
  • [6] Miettinen TA, 1997, CIRCULATION, V96, P4211
  • [7] *NAT CHOL ED PROGR, 1993, NIH PUBL
  • [8] Packard CJ, 1998, CIRCULATION, V97, P1440
  • [9] Lipoprotein changes and reduction in the incidence of major coronary heart disease events in the Scandinavian Simvastatin Survival Study
    Pedersen, TR
    Olsson, AG
    Færgeman, O
    Kjekshus, J
    Wedel, H
    Berg, K
    Wilhelmsen, L
    Haghfelt, T
    Thorgeirsson, G
    Pyörälä, K
    Miettinen, T
    Christophersen, B
    Tobert, JA
    Musliner, TA
    Cook, TJ
    [J]. CIRCULATION, 1998, 97 (15) : 1453 - 1460
  • [10] Influence of baseline lipids on effectiveness of pravastatin in the CARE trial
    Pfeffer, MA
    Sacks, FM
    Moyé, LA
    East, C
    Goldman, S
    Nash, DT
    Rouleau, JR
    Rouleau, JL
    Sussex, BA
    Theroux, P
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1999, 33 (01) : 125 - 130