Association between prior cytomegalovirus infection and the risk of restenosis after coronary atherectomy

被引:387
作者
Zhou, YF
Leon, MB
Waclawiw, MA
Popma, JJ
Yu, ZX
Finkel, T
Epstein, SE
机构
[1] NHLBI, CARDIOL BRANCH, BETHESDA, MD 20892 USA
[2] WASHINGTON HOSP CTR, WASHINGTON, DC 20010 USA
关键词
D O I
10.1056/NEJM199608293350903
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Restenosis occurs commonly after coronary angioplasty and atherectomy, but the causes of restenosis are poorly understood. Recently, it has been found that cytomegalovirus (CMV) DNA is present in restenotic lesions from atherectomy specimens. This and other evidence suggest that CMV may have a role in the process of restenosis. Methods We prospectively studied 75 consecutive patients undergoing directional coronary atherectomy for symptomatic coronary artery disease. Before atherectomy was performed, we measured blood levels of anti-CMV IgG antibodies to determine whether previous exposure to CMV increased the risk of restenosis, as determined by coronary angiography performed six months after atherectomy. Results After atherectomy, the mean (+/-SD) minimal luminal diameter of the target vessel was greater in the 49 patients who were seropositive for CMV than in the 26 patients who were seronegative (3.18+/-0.51 mm vs. 2.89+/-0.45 mm, P=0.01). After six months, however, the seropositive patients had a greater reduction in the luminal diameter (1.24+/-0.83 mm vs, 0.68+/-0.69 mm, P=0.003), resulting in a significantly higher rate of restenosis in the seropositive patients (43 percent vs. 8 percent, P=0.002). In a multivariable logistic-regression model, CMV seropositivity and the CMV titer were independently predictive of restenosis (odds ratios, 12.9 and 8.1, respectively). There was no evidence of acute infection, since the titer of anti-CMV IgG antibodies did not increase over time and tests for anti-CMV IgM antibodies were negative in all patients. Conclusions Prior infection with CMV is a strong independent risk factor for restenosis after coronary atherectomy. If confirmed, these findings may help identify patients at risk for restenosis. (C) 1996, Massachusetts Medical Society.
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页码:624 / 630
页数:7
相关论文
共 31 条
[1]   INDUCTION OF AN ENDOTHELIAL-CELL GROWTH-FACTOR BY HUMAN CYTOMEGALOVIRUS-INFECTION OF FIBROBLASTS [J].
ALCAMI, J ;
BARZU, T ;
MICHELSON, S .
JOURNAL OF GENERAL VIROLOGY, 1991, 72 :2765-2770
[2]  
BACH R, 1994, THROMB RES, V74, pS55
[3]   HERPESVIRUSES - IMMUNE ESCAPE ARTISTS [J].
BANKS, TA ;
ROUSE, BT .
CLINICAL INFECTIOUS DISEASES, 1992, 14 (04) :933-941
[4]   CYTOMEGALOVIRUS AND LATENCY - AN OVERVIEW [J].
BRUGGEMAN, CA .
VIRCHOWS ARCHIV B-CELL PATHOLOGY INCLUDING MOLECULAR PATHOLOGY, 1993, 64 (06) :325-333
[5]   EFFECT OF SERUM-LIPID CONCENTRATIONS ON RESTENOSIS AFTER SUCCESSFUL DE-NOVO PERCUTANEOUS TRANSLUMINAL CORONARY ANGIOPLASTY IN PATIENTS WITH TOTAL CHOLESTEROL 160 TO 240 MG/DL AND TRIGLYCERIDES LESS-THAN-350 MG/DL [J].
DZAVIK, V ;
TEO, KK ;
YOKOYAMA, S ;
MODI, R ;
DINWOODIE, A ;
BURTON, JR ;
TYMCHAK, WJ ;
MONTAGUE, TJ .
AMERICAN JOURNAL OF CARDIOLOGY, 1995, 75 (14) :936-938
[6]   VIRAL ACTIVATION OF THE COAGULATION CASCADE - MOLECULAR-INTERACTIONS AT THE SURFACE OF INFECTED ENDOTHELIAL-CELLS [J].
ETINGIN, OR ;
SILVERSTEIN, RL ;
FRIEDMAN, HM ;
HAJJAR, DP .
CELL, 1990, 61 (04) :657-662
[7]   VONWILLEBRAND-FACTOR MEDIATES PLATELET-ADHESION TO VIRALLY INFECTED ENDOTHELIAL-CELLS [J].
ETINGIN, OR ;
SILVERSTEIN, RL ;
HAJJAR, DP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (11) :5153-5156
[8]  
FAXON DP, 1995, ANN NY ACAD SCI, V748, P419
[9]   INFLUENCE OF CORONARY VESSEL SIZE ON RENARROWING PROCESS AND LATE ANGIOGRAPHIC OUTCOME AFTER SUCCESSFUL BALLOON ANGIOPLASTY [J].
FOLEY, DP ;
MELKERT, R ;
SERRUYS, PW .
CIRCULATION, 1994, 90 (03) :1239-1251
[10]   THE IMMEDIATE EARLY GENES OF HUMAN CYTOMEGALOVIRUS UP-REGULATE EXPRESSION OF THE INTERLEUKIN-2 AND INTERLEUKIN-2 RECEPTOR GENES [J].
GEIST, LJ ;
MONICK, MM ;
STINSKI, MF ;
HUNNINGHAKE, GW .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1991, 5 (03) :292-296