Increased plasma antigen levels of monocyte chemoattractant protein-1 in patients with restenosis after percutaneous transluminal coronary angioplasty

被引:26
作者
Hokimoto, S
Ogawa, H
Saito, T
Oshima, S
Noda, K
Soejima, H
Takazoe, K
Date, H
Ishibashi, F
Nakamura, S
Yasue, H
机构
[1] Kumamoto Univ, Sch Med, Dept Cardiovasc Med, Kumamoto 8608556, Japan
[2] Kumamoto Cent Hosp, Dept Cardiovasc Med, Kumamoto, Japan
来源
JAPANESE CIRCULATION JOURNAL-ENGLISH EDITION | 2000年 / 64卷 / 11期
关键词
angioplasty; coronary artery disease; restenosis;
D O I
10.1253/jcj.64.831
中图分类号
N09 [自然科学史]; B [哲学、宗教];
学科分类号
01 ; 0101 ; 010108 ; 060207 ; 060305 ; 0712 ;
摘要
Monocyte chemoattractant protein-1 (MCP-1) plays an important role in the progression of atherosclerosis in coronary arteries. To examine whether or not plasma antigen levels of MCP-1 are related to restenosis after percutaneous transluminal coronary angioplasty (PTCA), the plasma antigen levels of MCP-1 were measured by enzyme-linked immunosorbent assay (pg/ml) before, 24 and 48 h, and 3 months after elective PTCA for stable exertional angina performed between June 1997 and March 1998. Restenosis was defined as recurrence of stenosis greater than 50% of the diameter in the dilated segment at 3-month follow-up angiography. There were no differences in plasma MCP-1 antigen levels before and at 24 h after PTCA between restenosis (R; n=27) and norestenosis (N; n=43) groups (R vs N: 633+/-35 vs 589+/-34, and 669+/-41 vs 575+/-36 pg/ml before and at 24 h after PTCA, respectively), but plasma MCP-1 antigen levels were higher at 48 h and 3 months after PTCA in the R than in N group (R vs N: 678+/-41 vs 558+/-35, and 735+/-35 vs 571+/-32 pg/ml at 48 h and 3 months after PTCA, respectively). These data suggest that the MCP-1 production and macrophage accumulation in the balloon-injured site is partially associated with restenosis after PTCA.
引用
收藏
页码:831 / 834
页数:4
相关论文
共 16 条
[1]   INTIMAL PROLIFERATION OF SMOOTH-MUSCLE CELLS AS AN EXPLANATION FOR RECURRENT CORONARY-ARTERY STENOSIS AFTER PERCUTANEOUS TRANS-LUMINAL CORONARY ANGIOPLASTY [J].
AUSTIN, GE ;
RATLIFF, NB ;
HOLLMAN, J ;
TABEI, S ;
PHILLIPS, DF .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1985, 6 (02) :369-375
[2]   Decreased lesion formation in CCR2-/- mice reveals a role for chemokines in the initiation of atherosclerosis [J].
Boring, L ;
Gosling, J ;
Cleary, M ;
Charo, IF .
NATURE, 1998, 394 (6696) :894-897
[3]   MONOCYTES MAY AMPLIFY THEIR RECRUITMENT INTO INFLAMMATORY LESIONS BY INDUCING MONOCYTE CHEMOTACTIC PROTEIN [J].
CUSHING, SD ;
FOGELMAN, AM .
ARTERIOSCLEROSIS AND THROMBOSIS, 1992, 12 (01) :78-82
[4]   MINIMALLY MODIFIED LOW-DENSITY-LIPOPROTEIN INDUCES MONOCYTE CHEMOTACTIC PROTEIN-1 IN HUMAN ENDOTHELIAL-CELLS AND SMOOTH-MUSCLE CELLS [J].
CUSHING, SD ;
BERLINER, JA ;
VALENTE, AJ ;
TERRITO, MC ;
NAVAB, M ;
PARHAMI, F ;
GERRITY, R ;
SCHWARTZ, CJ ;
FOGELMAN, AM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (13) :5134-5138
[5]  
HOLMES DR, 1984, AM J CARDIOL SC, V53, P77
[6]   RESTENOSIS AFTER CORONARY ANGIOPLASTY - POTENTIAL BIOLOGIC DETERMINANTS AND ROLE OF INTIMAL HYPERPLASIA [J].
LIU, MW ;
ROUBIN, GS ;
KING, SB .
CIRCULATION, 1989, 79 (06) :1374-1387
[7]   Macrophage infiltration predicts restenosis after coronary intervention in patients with unstable angina [J].
Moreno, PR ;
Bernardi, VH ;
LopezCuellar, J ;
Newell, JB ;
McMellon, C ;
Gold, HK ;
Palacios, IF ;
Fuster, V ;
Fallon, JT .
CIRCULATION, 1996, 94 (12) :3098-3102
[8]   MONOCYTE CHEMOATTRACTANT PROTEIN-1 IN HUMAN ATHEROMATOUS PLAQUES [J].
NELKEN, NA ;
COUGHLIN, SR ;
GORDON, D ;
WILCOX, JN .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 88 (04) :1121-1127
[9]   Simultaneous elevation of the levels of circulating monocyte chemoattractant protein-1 and tissue factor in acute coronary syndromes [J].
Nishiyama, K ;
Ogawa, H ;
Yasue, H ;
Soejima, H ;
Misumi, K ;
Takazoe, K ;
Yoshimura, M ;
Kugiyama, K ;
Tsuji, I ;
Kumeda, K .
JAPANESE CIRCULATION JOURNAL-ENGLISH EDITION, 1998, 62 (09) :710-712
[10]   Monocyte chemoattractant protein-1 but not tumor necrosis factor-α is correlated with monocyte infiltration in mouse lipid lesions [J].
Reckless, J ;
Rubin, EM ;
Verstuyft, JB ;
Metcalfe, JC ;
Grainger, DJ .
CIRCULATION, 1999, 99 (17) :2310-2316