Effects of fluvastatin on coronary atherosclerosis in patients with mild to moderate cholesterol elevations (lipoprotein and coronary atherosclerosis study [LCAS])

被引:272
作者
Herd, JA
Ballantyne, CM
Farmer, JA
Ferguson, JJ
Jones, PH
West, S
Gould, KL
Gotto, AM
机构
[1] CORNELL UNIV, MED CTR, COLL MED, NEW YORK, NY 10021 USA
[2] BAYLOR COLL MED, DEPT MED, HOUSTON, TX 77030 USA
[3] UNIV TEXAS, SCH MED, DEPT MED, HOUSTON, TX 77030 USA
关键词
D O I
10.1016/S0002-9149(97)00346-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Despite the potential for reduced morbidity and mortality, aggressive intervention against mild to moderate hypercholesterolemia in patients with coronary heart disease (CHD) remains controversial and infrequently practiced. Eligible patients in the 2.5-year Lipoprotein and Coronary Atherosclerosis Study were men and women aged 35 to 75 years with angiographic CHD and mean low-density lipoprotein (LDL) cholesterol of 115 to 190 mg/dl despite diet. Patients (n = 429; 19% women) were randomized to fluvastatin 20 mg twice daily or placebo. One fourth of patients were also assigned open-label adjunctive cholestyramine up to 12 g/day because prerandomization LDL cholesterol remained greater than or equal to 160 mg/dl. The primary end point, assessed by quantitative coronary angiography, was within-patient perlesion change in minimum lumen diameter (MLD) of qualifying lesions. Across 2.5 years, mean LDL cholesterol was reduced by 23.9% in all fluvastatin patients (+/- cholestyramine) (146 to 111 mg/dl) and by 22.5% in the fluvastatin only subgroup (137 to 106 mg/dl). Primary end point analysis (340 patients) showed significantly less lesion progression in all fluvastatin versus all placebo patients, Delta MLD -0.028 versus -0.100 mm (p <0.01), and for fluvastatin alone versus placebo alone, Delta MLD -0.024 versus -0.094 mm (p <0.02). A consistent angiographic benefit with treatment was seen whether baseline LDL cholesterol was above or below 160 or 130 mg/dl. Beneficial trends with treatment were also consistently seen in clinical event rates but were not statistically significant. Thus, lipid lowering by fluvastatin in patients with mildly to moderately elevated LDL cholesterol significantly slowed CHD progression. (C) 1997 by Excerpta Medica, Inc.
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页码:278 / 286
页数:9
相关论文
共 30 条
  • [1] ANDERSON JA, 1984, J R STAT SOC B, V46, P1
  • [2] [Anonymous], 1994, CIRCULATION
  • [3] Aviram M, 1996, EUR J CLIN CHEM CLIN, V34, P599
  • [4] Progression of coronary artery disease predicts clinical coronary events - Long-term follow-up from the Cholesterol Lowering Atherosclerosis Study
    Azen, SP
    Mack, WJ
    CashinHemphill, L
    LaBree, L
    Shircore, AM
    Selzer, RH
    Blankenhorn, DH
    Hodis, HN
    [J]. CIRCULATION, 1996, 93 (01) : 34 - 41
  • [5] CORONARY ANGIOGRAPHIC CHANGES WITH LOVASTATIN THERAPY - THE MONITORED ATHEROSCLEROSIS REGRESSION STUDY (MARS)
    BLANKENHORN, DH
    AZEN, SP
    KRAMSCH, DM
    MACK, WJ
    CASHINHEMPHILL, L
    HODIS, HN
    DEBOER, LWV
    MAHRER, PR
    MASTELLER, MJ
    VAILAS, LI
    ALAUPOVIC, P
    HIRSCH, LJ
    [J]. ANNALS OF INTERNAL MEDICINE, 1993, 119 (10) : 969 - 976
  • [6] BENEFICIAL-EFFECTS OF COMBINED COLESTIPOL-NIACIN THERAPY ON CORONARY ATHEROSCLEROSIS AND CORONARY VENOUS BYPASS GRAFTS
    BLANKENHORN, DH
    NESSIM, SA
    JOHNSON, RL
    SANMARCO, ME
    AZEN, SP
    CASHINHEMPHILL, L
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1987, 257 (23): : 3233 - 3240
  • [7] LIPID-LOWERING AND PLAQUE REGRESSION - NEW INSIGHTS INTO PREVENTION OF PLAQUE DISRUPTION AND CLINICAL EVENTS IN CORONARY-DISEASE
    BROWN, BG
    ZHAO, XQ
    SACCO, DE
    ALBERS, JJ
    [J]. CIRCULATION, 1993, 87 (06) : 1781 - 1791
  • [8] 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
  • [9] Campeau L, 1997, NEW ENGL J MED, V336, P153
  • [10] CLEEMAN JI, 1988, ARCH INTERN MED, V148, P36, DOI 10.1001/archinte.148.1.36