Increased serum concentrations of interleukin-1 beta in patients with coronary artery disease

被引:75
作者
Hasdai, D
Scheinowitz, M
Leibovitz, E
Sclarovsky, S
Eldar, M
Barak, V
机构
[1] HEBREW UNIV JERUSALEM, HADASSAH MED CTR, DEPT ONCOL, IMMUNOL LAB TUMOUR DIAGNOSIS, JERUSALEM, ISRAEL
[2] TEL AVIV UNIV, BEILINSON MED CTR, DEPT CARDIOL, IL-49100 PETAH TIQWA, ISRAEL
[3] TEL AVIV UNIV, CHAIM SHEBA MED CTR, NEUFELD CARDIAC RES INST, IL-52621 TEL HASHOMER, ISRAEL
关键词
interleukin-1; beta; inflammation; atherosclerosis;
D O I
10.1136/hrt.76.1.24
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective-To assess serum interleukin-1 beta(IL-1 beta) concentrations in patients with ischaemic heart disease, to characterise subgroups of patients with raised IL-1 beta concentrations, and to examine whether serum IL-1 beta concentrations correlate with non-specific indices of inflammation. Design-Survey study of patients with ischaemic heart disease. Setting-Cardiac catheterisation laboratory of a tertiary medical centre. Patients-Consecutive patients with angina pectoris and patients recovering from uncomplicated acute myocardial infarction and undergoing elective coronary angiography. Results-Mean(SD) serum IL-1 beta concentrations were higher (P < 0.001) in patients with angina and <50% coronary artery stenosis (n = 11; 18.8(19.9) pg/ml), patients with angina greater than or equal to 50% stenosis (n = 23; 10.2(11.4 pg/ml), and patients 8(0.8) days post-infarction (n = 13; 4.4(5.8) pg/ml) than in 15 healthy, age-matched controls (0.3(0.5) pg/ml). Serum IL-1 beta concentrations did not correlate with total blood leucocyte counts (r = -0.07, P = NS), blood lymphocyte counts (r = -0.24, P = NS), and blood monocyte counts (r = -0.29, P = NS), or with fibrinogen (r = -0.16, P = NS) and C-reactive protein concentrations (9(10.5) mg/dl v 14.1(19) mg/dl for patients with undetectable and detectable concentrations, respectively, P = NS). Conclusion-Serum IL-1 beta concentrations are raised in patients with ischaemic heart disease, in particular in those with minimal coronary artery disease and angina. The precise role of IL-1 beta in coronary artery disease remains to be determined.
引用
收藏
页码:24 / 28
页数:5
相关论文
共 42 条
[1]  
ALEXANDER HR, 1992, SURGERY, V112, P188
[2]   ELEVATION OF C-REACTIVE PROTEIN IN ACTIVE CORONARY-ARTERY DISEASE [J].
BERK, BC ;
WEINTRAUB, WS ;
ALEXANDER, RW .
AMERICAN JOURNAL OF CARDIOLOGY, 1990, 65 (03) :168-172
[3]   INTERLEUKIN-1 (IL-1) INDUCES BIOSYNTHESIS AND CELL-SURFACE EXPRESSION OF PROCOAGULANT ACTIVITY IN HUMAN VASCULAR ENDOTHELIAL-CELLS [J].
BEVILACQUA, MP ;
POBER, JS ;
MAJEAU, GR ;
COTRAN, RS ;
GIMBRONE, MA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1984, 160 (02) :618-623
[4]   INTERLEUKIN-1-ALPHA AS A FACTOR IN OCCLUSIVE VASCULAR-DISEASE [J].
BRODY, JI ;
PICKERING, NJ ;
CAPUZZI, DM ;
FINK, GB ;
CAN, CA ;
GOMEZ, F .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 1992, 97 (01) :8-13
[5]   INTERLEUKIN-1 PRETREATMENT DECREASES ISCHEMIA REPERFUSION INJURY [J].
BROWN, JM ;
WHITE, CW ;
TERADA, LS ;
GROSSO, MA ;
SHANLEY, PF ;
MULVIN, DW ;
BANERJEE, A ;
WHITMAN, GJR ;
HARKEN, AH ;
REPINE, JE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (13) :5026-5030
[6]  
CALDERON TM, 1994, LAB INVEST, V70, P836
[7]   MECHANISM OF CYTOKINE INHIBITION OF BETA-ADRENERGIC AGONIST STIMULATION OF CYCLIC-AMP IN RAT CARDIAC MYOCYTES - IMPAIRMENT OF SIGNAL TRANSDUCTION [J].
CHUNG, MK ;
GULICK, TS ;
ROTONDO, RE ;
SCHREINER, GF ;
LANGE, LG .
CIRCULATION RESEARCH, 1990, 67 (03) :753-763
[8]   IN-VIVO BLOCKADE OF TUMOR NECROSIS FACTOR-A IN CHOLESTEROL-FED RABBITS AFTER CARDIAC TRANSPLANT INHIBITS ACUTE CORONARY-ARTERY NEOINTIMAL FORMATION [J].
CLAUSELL, N ;
MOLOSSI, S ;
SETT, S ;
RABINOVITCH, M .
CIRCULATION, 1994, 89 (06) :2768-2779
[9]  
CLAUSELL N, 1993, AM J PATHOL, V142, P1772
[10]   UP-REGULATION OF FIBRONECTIN SYNTHESIS BY INTERLEUKIN-1-BETA IN CORONARY-ARTERY SMOOTH-MUSCLE CELLS IS ASSOCIATED WITH THE DEVELOPMENT OF THE POST-CARDIAC TRANSPLANT ARTERIOPATHY IN PIGLETS [J].
CLAUSELL, N ;
RABINOVITCH, M .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (04) :1850-1858