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PPAR Gamma Expression Levels during Development of Heart Failure in Patients with Coronary Artery Disease after Coronary Artery Bypass-Grafting

机译:冠状动脉旁路移植术后冠心病患者心力衰竭发展过程中的PPARγ表达水平

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Genetic research has elucidated molecular mechanisms of heart failure (HF). Peroxisome proliferator-activated receptors (PPARs) seem to be important in etiology of HF. The aim of study was to find the correlation between PPARγexpression during development of HF in patients and coronary artery disease (CAD) after coronary artery bypass-grafting (CABG).Methods and Results. We followed up 157 patients (mean age 63) with CAD without clinical, laboratory, or echo parameters of HF who underwent CABG. Clinical and laboratory status were assessed before CABG and at 1, 12, and 24 months. During CABG slices of aorta (Ao) and LV were collected for genetic research. HF was defined as LVEF <40% or NT-proBNP >400 pg/mL or 6MWT <400 m. Patients were divided into 2 groups: with and without HF. PPARγexpression in Ao and LV was not increased in both groups at 2-year follow-up. Sensitivity of PPARγexpression in Ao above 1.1075 in detection of HF was 20.5% (AUC 0.531, 95% CI 0.442–0.619). Positive predictive value (Ppv) was 85.7%. Sensitivity and specificity of PPARγexpression in the LV in detection of HF were 58% and 92.9%, respectively (AUC 0.540, 95% CI 0.452–0.626). Ppv was 73.2%.Conclusion. PPARγexpression in Ao and LV was comparable and should not be used as predictive factor for development of HF in patients with CAD after CABG.
机译:遗传研究阐明了心力衰竭(HF)的分子机制。过氧化物酶体增殖物激活受体(PPARs)似乎在HF的病因中很重要。本研究的目的是发现患者心力衰竭期间PPARγ的表达与冠状动脉搭桥术(CABG)后冠状动脉疾病(CAD)的相关性。方法与结果。我们随访了157例接受CABG的无临床,实验室或HF回声参数的CAD患者(平均年龄63岁)。在CABG之前以及1、12和24个月时评估临床和实验室状态。在CABG期间,收集主动脉(Ao)和LV的切片用于遗传研究。 HF定义为LVEF <40%或NT-proBNP> 400µpg / mL或6MWT <400µm。患者分为两组:有和没有HF。在2年的随访中,两组的Ao和LV中的PPARγ表达均未升高。在Ao中,高于1.1075的Ao中PPARγ表达的敏感性为20.5%(AUC 0.531,95%CI 0.442-0.619)。阳性预测值(Ppv)为85.7%。检测HF时左心室中PPARγ表达的敏感性和特异性分别为58%和92.9%(AUC 0.540,95%CI 0.452-0.626)。 Ppv为73.2%。结论。在CABG后,CAD患者CAD中Ao和LV中PPARγ的表达具有可比性,不应用作预测HF发生的预测因素。

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