Randomized secondary prevention trial of azithromycin in patients with coronary artery disease and serological evidence for Chlamydia pneumoniae infection -: The azithromycin in coronary artery disease:: Elimination of myocardial infection with Chlamydia (ACADEMIC) study

被引:254
作者
Anderson, JL [1 ]
Muhlestein, JB [1 ]
Carlquist, J [1 ]
Allen, A [1 ]
Trehan, S [1 ]
Nielson, C [1 ]
Hall, S [1 ]
Brady, J [1 ]
Egger, M [1 ]
Horne, B [1 ]
Lim, T [1 ]
机构
[1] LDS Hosp, Div Cardiol, Dept Med, Salt Lake City, UT 84143 USA
关键词
Chlamydia pneumoniae; antibiotics; coronary disease;
D O I
10.1161/01.CIR.99.12.1540
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-Chlamydia pneumoniae commonly causes respiratory infection, is vasotropic, causes atherosclerosis in animal models, and has been found in human atheromas. Whether it plays a causal role in clinical coronary artery disease (CAD) and is amenable to antibiotic therapy is uncertain, Methods and Results-CAD patients (n=302) who had a seropositive reaction to C pneumoniae (IgG titers greater than or equal to 1:16) were randomized to receive placebo or azithromycin, 500 mg/d for 3 days, then 500 mg/wk for 3 months. Circulating markers of inflammation (C-reactive protein [CRP], interleukin [IL]-1, IL-6, and tumor necrosis factor [TNF]-alpha), C pneumoniae antibody titers, and cardiovascular events were assessed at 3 and 6 months. Treatment groups were balanced, with age averaging 64 (SD=10) years; 89% of the patients were male. Azithromycin reduced a global rank sum score of the 4 inflammatory markers at 6 (but not 3) months (P=0.011) as well as the mean global rank sum change score: 531 (SD=201) for active drugs and 587 (SD=190) for placebo (P=0.027). Specifically, change-score ranks were significantly lower for CRP (P=0.011) and IL-6 (P=0.043). Antibody titers were unchanged, and number of clinical cardiovascular events at 6 months did not differ by therapy (9 for active drug, 7 for placebo). Azithromycin decreased infections requiring antibiotics (1 versus 12 at 3 months, P=0.002) but caused more mild, primarily gastrointestinal, adverse effects (36 versus 17, P=0.003), Conclusions-In CAD patients positive for C pneumoniae antibodies, global tests of 4 markers of inflammation improved at 6 months with azithromycin. However, unlike another smaller study, no differences in antibody titers and clinical events were observed. Longer-term and larger studies of antichlamydial therapy are indicated.
引用
收藏
页码:1540 / 1547
页数:8
相关论文
共 38 条
[1]   SEROEPIDEMIOLOGY OF CHLAMYDIA-PNEUMONIAE TWAR INFECTION IN SEATTLE FAMILIES, 1966-1979 [J].
ALDOUS, MB ;
GRAYSTON, JT ;
WANG, SP ;
FOY, HM .
JOURNAL OF INFECTIOUS DISEASES, 1992, 166 (03) :646-649
[2]   Evaluation of C-reactive protein, an inflammatory marker, and infectious serology as risk factors for coronary artery disease and myocardial infarction [J].
Anderson, JL ;
Carlquist, JF ;
Muhlestein, JB ;
Horne, BD ;
Elmer, SP .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1998, 32 (01) :35-41
[3]   PERSISTENT CHLAMYDIAE - FROM CELL-CULTURE TO A PARADIGM FOR CHLAMYDIAL PATHOGENESIS [J].
BEATTY, WL ;
MORRISON, RP ;
BYRNE, GI .
MICROBIOLOGICAL REVIEWS, 1994, 58 (04) :686-699
[4]   C-REACTIVE PROTEIN INDUCES HUMAN PERIPHERAL-BLOOD MONOCYTES TO SYNTHESIZE TISSUE FACTOR [J].
CERMAK, J ;
KEY, NS ;
BACH, RR ;
BALLA, J ;
JACOB, HS ;
VERCELLOTTI, GM .
BLOOD, 1993, 82 (02) :513-520
[5]  
DAGOSTINO RB, 1998, ENCY BIOSTATISTICS, V4, P2749
[6]  
Farmer JA, 1997, HEART DIS TXB CARDIO, V5, P1126
[7]   Rabbit model for Chlamydia pneumoniae infection [J].
Fong, IW ;
Chiu, B ;
Viira, E ;
Fong, MW ;
Jang, D ;
Mahony, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 1997, 35 (01) :48-52
[8]  
GANAPATHI MK, 1991, J IMMUNOL, V147, P1261
[9]   Replication of Chlamydia pneumoniae in vitro in human macrophages, endothelial cells, and aortic artery smooth muscle cells [J].
Gaydos, CA ;
Summersgill, JT ;
Sahney, NN ;
Ramirez, JA ;
Quinn, TC .
INFECTION AND IMMUNITY, 1996, 64 (05) :1614-1620
[10]   INFECTIONS CAUSED BY CHLAMYDIA-PNEUMONIAE STRAIN TWAR [J].
GRAYSTON, JT .
CLINICAL INFECTIOUS DISEASES, 1992, 15 (05) :757-763