Rationale and design of a secondary prevention trial of antibiotic use in patients after myocardial infarction: The WIZARD (weekly intervention with zithromax [azithromycin] for atherosclerosis and its related disorders) trial

被引:49
作者
Dunne, MW [1 ]
机构
[1] Pfizer Inc, Cent Res, Groton, CT 06340 USA
关键词
D O I
10.1086/315634
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Mounting evidence supports the contention that atherosclerosis is an inflammatory disease. Recently a possible role far infectious microorganisms has gathered attention. Chlamydia pneumoniae is one possible pathogen. If C. pneumoniae is a target organism, antibiotics with antichlamydial activity may be able to ameliorate plaque instability. The WIZARD trial is a secondary prevention study that is assessing the impact of a 3-month course of azithromycin compared with placebo on the progression of clinical coronary heart disease. The study will enroll 3300 patients who have had a prior myocardial infarction and who have a C. pneumoniae IgG titer of greater than or equal to 1:16. The primary end point is a composite of time to either recurrent myocardial infarction, death, a revascularization procedure, or hospitalization for angina. This study is the first of a series of adequately powered clinical trials that will attempt to bridge insights from preclinical investigations to interventions applicable to patient care.
引用
收藏
页码:S572 / S578
页数:7
相关论文
共 24 条
  • [1] SEROEPIDEMIOLOGY OF CHLAMYDIA-PNEUMONIAE TWAR INFECTION IN SEATTLE FAMILIES, 1966-1979
    ALDOUS, MB
    GRAYSTON, JT
    WANG, SP
    FOY, HM
    [J]. JOURNAL OF INFECTIOUS DISEASES, 1992, 166 (03) : 646 - 649
  • [2] PERSISTENT CHLAMYDIAE - FROM CELL-CULTURE TO A PARADIGM FOR CHLAMYDIAL PATHOGENESIS
    BEATTY, WL
    MORRISON, RP
    BYRNE, GI
    [J]. MICROBIOLOGICAL REVIEWS, 1994, 58 (04) : 686 - 699
  • [3] High prevalence of Chlamydia pneumoniae DNA in peripheral blood mononuclear cells in patients with cardiovascular disease and in middle-aged blood donors
    Boman, J
    Söderberg, S
    Forsberg, J
    Birgander, LS
    Allard, A
    Persson, K
    Jidell, E
    Kumlin, U
    Juto, P
    Waldenström, A
    Wadell, G
    [J]. JOURNAL OF INFECTIOUS DISEASES, 1998, 178 (01) : 274 - 277
  • [4] DUNNE M, 1998, EMERG INFECT DIS, V2, P105
  • [5] Dunne Michael W., 1997, American Journal of Medicine, V102, P37
  • [6] AZITHROMYCIN-INDUCED BLOCK OF ELEMENTARY BODY FORMATION IN CHLAMYDIA-TRACHOMATIS
    ENGEL, JN
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1992, 36 (10) : 2304 - 2309
  • [7] THE INVITRO ANTIBIOTIC SUSCEPTIBILITY OF CHLAMYDIA-PNEUMONIAE
    FENELON, LE
    MUMTAZ, G
    RIDGWAY, GL
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1990, 26 (06) : 763 - 767
  • [8] Rabbit model for Chlamydia pneumoniae infection
    Fong, IW
    Chiu, B
    Viira, E
    Fong, MW
    Jang, D
    Mahony, J
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1997, 35 (01) : 48 - 52
  • [9] INFECTIONS CAUSED BY CHLAMYDIA-PNEUMONIAE STRAIN TWAR
    GRAYSTON, JT
    [J]. CLINICAL INFECTIOUS DISEASES, 1992, 15 (05) : 757 - 763
  • [10] HAHN DL, 1995, J FAM PRACTICE, V41, P345