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Therapeutic effects of different Atorvastatin doses on vulnerable plaques in coronary arteries assessed by intracoronary optical coherence tomography

机译:通过冠状动脉内光学相干断层扫描评估不同阿托伐他汀剂量对冠状动脉易损斑块的治疗作用

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摘要

The aim of this study was to evaluate optical coherence tomography (OCT) as an assessment of the efficacy of atorvastatin treatment.Twenty-four acute coronary syndrome (ACS) patients were allocated to conventional-dose (20 mg atorvastatin, n = 12) and intensive-dose (40–80 mg atorvastatin, n = 12) groups and correlations between changes in the OCT measurements and blood routine indexes were analyzed 9 months post-percutaneous coronary intervention (PCI).Treatment with atorvastatin resulted in a significant increase in the target thin cap fibroatheroma (TCFA) fibrous cap thicknesses in both groups. The increase was bigger in the intensive-dose group than in the conventional-dose group (184.1 ± 57.4 μm vs. 125.1 ± 28.6, P = .005). The TCFA lipid core arc in both groups was significantly decreased compared with baseline (72.9 ± 29.3 vs. 127.6 ± 50.8, P < .01 and 74.6 ± 32.9 vs. 132.6 ± 51.3, P < .01, respectively). Correlation analyses showed an inverse relationship between low-density lipoprotein cholesterol (LDL-c) levels and the TCFA cap thickness, and a direct relationship between C-reactive protein (CRP) level and lipid core arc.Statins significantly increased the TCFA fibrous cap thickness and reduced the lipid core arc, and OCT measurements accurately reflected the levels of blood LDL-c and CRP.Trial registration: (Chinese Clinical Trial Registry) ChiCTR-IPR-17010874
机译:这项研究的目的是评估光学相干断层扫描(OCT)作为对阿托伐他汀治疗效果的评估.24例急性冠脉综合征(ACS)患者被分配为常规剂量(20 mg阿托伐他汀,n = 12)和在经皮冠状动脉介入治疗(PCI)9个月后,分析了大剂量(40-80 mg阿托伐他汀,n = 12)组和OCT测量值变化与血液常规指标之间的相关性。用阿托伐他汀治疗可显着增加两组均以薄帽纤维瘤(TCFA)纤维帽厚度为目标。与常规剂量组相比,高剂量组的增加更大(184.1±57.4μmvs. 125.1±28.6,P = 0.005)。与基线相比,两组的TCFA脂质核心弧均显着降低(分别为72.9±29.3和127.6±50.8,P <.01和74.6±32.9与132.6±51.3,P <0.01)。相关性分析显示低密度脂蛋白胆固醇(LDL-c)水平与TCFA帽厚度呈反比关系,而C反应蛋白(CRP)水平与脂质核心弧之间呈直接关系。他汀类药物显着增加TCFA纤维帽厚度并减少了脂质核心弧,OCT测量准确反映了血液中LDL-c和CRP的水平。试验注册:(中国临床试验注册中心)ChiCTR-IPR-17010874

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