Low basal levels of circulating adiponectin in patients undergoing coronary stenting predict in-stent restenosis, independently of basal levels of inflammatory markers: Lipoprotein associated phospholipase A2, and myeloperoxidase

被引:24
作者
Moldoveanu, Elena [1 ,2 ]
Mut-Vitcu, Bogdan [3 ]
Tanaseanu, George R. [4 ]
Marta, Daciana S.
Manea, Gabriela [2 ]
Kosaka, Tetsuya [5 ]
Vidulescu, Cristina [4 ]
Tanaseanu, Cristina [4 ]
机构
[1] Victor Babes Natl Inst Pathol & Biomed Res, Ultrastruct Pathol Dept, Bucharest 050096, Romania
[2] Titu Maiorescu Univ, Bucharest, Romania
[3] Inst Cardiovasc Dis, Timisoara, Romania
[4] Carol Davila Univ Med & Pharm, Bucharest, Romania
[5] Alfresa Pharma Corp, Diagnost R&D Dept, Osaka, Japan
关键词
In-stent restenosis; Adiponectin; Lipoprotein associated phospholipase A2; Myeloperoxidase;
D O I
10.1016/j.clinbiochem.2008.09.109
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Objective: The aim of this study was to find a pre-interventional marker with the capacity to Predict in-stent restenosis (ISR). Considering the anti-atherosclerotic role of adiponectin (APO). an adipocytokine with anti-inflammatory, anti-proliferative, anti-oxidative and anti-thrombotic properties. low plasma levels of APO might be correlated with the risk of ISR. We investigated the correlations between the plasma levels of APO and two markers of inflammation: lipoprotein associated phospholipase A2 (Lp-PLA2) and myeloperoxidase (MPO). Design and methods: 80 patients with angiographically significant stenosis underwent percutaneous coronary intervention (PCI)with bare metal stent. Plasma APO concentration and plasma Lp-PLA2 and MPO activities Were evaluated immediately before and after PCI. then followed up at 24, 48, 72 h and at 1, 3, 6 months respectively. ISR was evaluated at 6 months after stenting by follow-up coronary angiograms, and it was defined as > 50% stenosis of the target lesion. Results: ISR was Present in 31.75% of patients. Baseline APO plasma concentration. measured before PCI. was lower in ISR Patients than those without ISR [3.97 (+/- 1.05) vs 6.65 (+/- 2.95) mu g/mL respectively, p<0.001]. The Patients with APO values less than 4.9 mu g/mL at discharge were more susceptible to develop ISR (odd ratio. 4.27; 95% CI, 1.56-11.72,p<0.001). ISR rate was independent of inflammation markers Lp-PLA2 and MPO baseline values measured before PCI. Conclusions: The persistence of a low APO plasma level at discharge and 6 months afterwards may be used as a clinically useful marker for ISR prediction in patients undergoing PCI. (c) 2008 The Canadian Society of Clinical Chemists. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:1429 / 1433
页数:5
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