首页> 美国卫生研究院文献>BMJ Open >Proteomic prediction and Renin angiotensin aldosterone system Inhibition prevention Of early diabetic nephRopathy in TYpe 2 diabetic patients with normoalbuminuria (PRIORITY): essential study design and rationale of a randomised clinical multicentre trial
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Proteomic prediction and Renin angiotensin aldosterone system Inhibition prevention Of early diabetic nephRopathy in TYpe 2 diabetic patients with normoalbuminuria (PRIORITY): essential study design and rationale of a randomised clinical multicentre trial

机译:蛋白质组学预测和肾素血管紧张素醛固酮系统抑制TYpe 2糖尿病性白蛋白尿(PRIORITY)患者早期糖尿病肾病的预防:一项随机临床多中心试验的基本研究设计和理论基础

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摘要

IntroductionDiabetes mellitus affects 9% of the European population and accounts for 15% of healthcare expenditure, in particular, due to excess costs related to complications. Clinical trials aiming for earlier prevention of diabetic nephropathy by renin angiotensin system blocking treatment in normoalbumuric patients have given mixed results. This might reflect that the large fraction of normoalbuminuric patients are not at risk of progression, thereby reducing power in previous studies. A specific risk classifier based on urinary proteomics (chronic kidney disease (CKD)273) has been shown to identify normoalbuminuric diabetic patients who later progressed to overt kidney disease, and may hold the potential for selection of high-risk patients for early intervention. Combining the ability of CKD273 to identify patients at highest risk of progression with prescription of preventive aldosterone blockade only to this high-risk population will increase power. We aim to confirm performance of CKD273 in a prospective multicentre clinical trial and test the ability of spironolactone to delay progression of early diabetic nephropathy.
机译:引言糖尿病影响了9%的欧洲人口,占医疗保健支出的15%,特别是由于与并发症相关的额外费用。旨在通过正常尿白蛋白患者中的肾素血管紧张素系统阻断治疗来早期预防糖尿病肾病的临床试验得出了不同的结果。这可能反映出大部分白蛋白尿患者没有发展的风险,从而降低了先前研究的功效。研究表明,基于尿蛋白质组学的特定风险分类器(慢性肾脏病(CKD)273)可以识别出正常白蛋白尿型糖尿病患者,这些患者后来发展为明显的肾脏疾病,并且可能具有选择高危患者进行早期干预的潜力。将CKD273识别具有最高进展风险的患者的能力与仅对这一高危人群开具预防性醛固酮阻断的处方相结合,将会提高治疗能力。我们的目标是在一项前瞻性多中心临床试验中确认CKD273的性能,并测试螺内酯延迟糖尿病早期肾病进展的能力。

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