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Pre-clinical myocardial metabolic alterations in chronic kidney disease.

机译:慢性肾脏疾病的临床前心肌代谢改变。

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摘要

Cardiovascular disease (CVD) is the leading cause of morbidity and mortality in patients with chronic kidney disease (CKD) [1]. As a consequence, patients with CKD are considered at high risk and as coronary heart disease equivalent [2]. Different diagnostic algorithms are used in normal clinical practice to predict global cardiovascular risk; however, in CKD the utility of these tests is limited due to uremia-specific risk factors. As a result, it is necessary to explore CKD-specific diagnostic tools to help predict cardiovascular risk in patients with CKD.In this issue of Cardiology, Fink et al. [3] describe a novel method of assessing preclinical myocardial metabolic alterations as a marker of CVD in pre-dialysis patients with CKD. They employed quantitative F18-fluo-rodeoxyglucose positron emission tomography (FDG PET) as a means to measure myocardial glucose utilization (MGU) in 13 non-diabetic patients.
机译:心血管疾病(CVD)是慢性肾脏病(CKD)患者发病和死亡的主要原因[1]。结果,CKD患者被认为是高危人群,相当于冠心病[2]。正常临床实践中使用了不同的诊断算法来预测整体心血管疾病的风险。但是,在CKD中,由于特定于尿毒症的危险因素,这些测试的实用性受到限制。因此,有必要探索特定于CKD的诊断工具,以帮助预测CKD患者的心血管风险。 [3]描述了一种评估临床前心肌代谢变化作为CKD透析前患者CVD标记的新方法。他们采用定量F18-氟代-脱氧葡萄糖正电子发射断层扫描(FDG PET)作为测量13例非糖尿病患者心肌葡萄糖利用率(MGU)的方法。

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