Plasma asymmetric dimethylarginine predicts restenosis after coronary angioplasty

被引:18
作者
Derkacz, Arkadiusz [1 ]
Protasiewicz, Marcin [2 ]
Poreba, Rafal [1 ]
Doroszko, Adrian [1 ]
Poreba, Malgorzata [3 ]
Antonowicz-Juchniewicz, Jolanta [1 ]
Andrzejak, Ryszard [1 ]
Szuba, Andrzej [1 ]
机构
[1] Wroclaw Med Univ, Dept Internal Med Occupat Dis & Hypertens, PL-50556 Wroclaw, Poland
[2] Wroclaw Med Univ, Dept Cardiol, Wroclaw, Poland
[3] Wroclaw Med Univ, Dept Pathophysiol, Wroclaw, Poland
关键词
asymmetric dimethylarginine; percutaneous coronary intervention; bare metal stent; ENDOTHELIAL DYSFUNCTION; EVENTS; ADMA; RISK; CHOLESTEROL; INVOLVEMENT; ARTERY;
D O I
10.5114/aoms.2011.23410
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Asymmetric dimethylarginine (ADMA) is an endogenous competitive inhibitor of endothelial nitric oxide synthase. Asymmetric dimethylarginine may influence the process of restenosis after coronary angioplasty. The aim of the study was to determine if initial plasma ADMA level could predict restenosis after coronary angioplasty and stenting. Material and methods: The study group consisted of 60 consecutive patients (10 women and 50 men, average age 58.9 +/- 10.4 years old), who underwent percutaneous coronary angioplasty with bare metal stenting for stable coronary artery disease. All patients underwent follow-up coronary angiography after a 6-month period. Patients were divided into two groups, one with restenosis (n = 22), and the other one without restenosis (n = 38). In addition to measuring acknowledged restenosis risk factors, plasma ADMA level was measured before initial angiography. Results: Asymmetric dimethylarginine plasma level was significantly higher in the group with restenosis than in the group without restenosis (1.94 +/- 0.94 mu mol/l vs. 0.96 +/- 0.67 mu mol/l; p < 0.05). L-arginine/ADMA ratio was also decreased in the group with restenosis, when compared with the group without restenosis (p < 0.05). Multivariate logistic regression revealed that independent restenosis risk factors were characterised by an initially high ADMA level (p < 0.01), advanced age (p < 0.05) and low level of HDL cholesterol (p < 0.05). Conclusions: Pre-procedural elevated plasma ADMA level increases the risk of restenosis in patients who underwent coronary angioplasty and stenting with bare metal stents.
引用
收藏
页码:444 / 448
页数:5
相关论文
共 27 条
[1]   Asymmetrical dimethylarginine and severity of erectile dysfunction and their impact on cardiovascular events in patients with acute coronary syndrome [J].
Aktoz, Meryem ;
Aktoz, Tevfik ;
Tatli, Ersan ;
Kaplan, Mustafa ;
Turan, Fatma Nesrin ;
Barutcu, Ahmet ;
Atakan, Irfan Hueseyin ;
Demir, Muzaffer ;
Altun, Armagan .
ARCHIVES OF MEDICAL SCIENCE, 2010, 6 (02) :168-175
[2]   A novel predictor of restenosis and adverse cardiac events: asymmetric dimethylarginine [J].
Ari, Hasan ;
Ari, Selma ;
Erdogan, Ercan ;
Tiryakioglu, Osman ;
Ustundag, Yasemin ;
Huysal, Kagan ;
Koca, Vedat ;
Bozat, Tahsin .
HEART AND VESSELS, 2010, 25 (01) :19-26
[3]   Asymmetric dimethylarginine (ADMA):: A novel risk factor for endothelial dysfunction -: Its role in hypercholesterolemia [J].
Böger, RH ;
Bode-Böger, SM ;
Szuba, A ;
Tsao, PS ;
Chan, JR ;
Tangphao, O ;
Blaschke, TF ;
Cooke, JP .
CIRCULATION, 1998, 98 (18) :1842-1847
[4]   An endogenous inhibitor of nitric oxide synthase regulates endothelial adhesiveness for monocytes [J].
Böger, RH ;
Bode-Böger, SM ;
Tsao, PS ;
Lin, PS ;
Chan, JR ;
Cooke, JP .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2000, 36 (07) :2287-2295
[5]   LDL cholesterol upregulates synthesis of asymmetrical dimethylarginine in human endothelial cells -: Involvement of S-adenosylmethionine-dependent methyltransferases [J].
Böger, RH ;
Sydow, K ;
Borlak, J ;
Thum, T ;
Lenzen, H ;
Schubert, B ;
Tsikas, D ;
Bode-Böger, SM .
CIRCULATION RESEARCH, 2000, 87 (02) :99-105
[6]  
Chan AW, 2003, TXB INTERVENTIONAL C, P415
[7]   High preprocedural non-HDL cholesterol is associated, with enhanced oxidative stress and monocyte activation after coronary angioplasty: possible implications in restenosis [J].
Cipollone, F ;
Fazia, M ;
Iezzi, A ;
Pini, B ;
Costantini, F ;
De Cesare, D ;
Paloscia, L ;
Materazzo, G ;
D'Annunzio, E ;
Bucciarelli, T ;
Vecchiet, J ;
Chiarelli, F ;
Cuccurullo, F ;
Mezzetti, A .
HEART, 2003, 89 (07) :773-779
[8]  
FISHMAN JA, 1975, LAB INVEST, V32, P339
[9]   NITRIC OXIDE-GENERATING VASODILATORS AND 8-BROMO-CYCLIC GUANOSINE-MONOPHOSPHATE INHIBIT MITOGENESIS AND PROLIFERATION OF CULTURED RAT VASCULAR SMOOTH-MUSCLE CELLS [J].
GARG, UC ;
HASSID, A .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 83 (05) :1774-1777
[10]   Nitric oxide synthase inhibitors and hypertension in children and adolescents [J].
Goonasekera, CDA ;
Rees, DD ;
Woolard, P ;
Frend, A ;
Shah, V ;
Dillon, MJ .
JOURNAL OF HYPERTENSION, 1997, 15 (08) :901-909