首页> 外文OA文献 >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糖尿病性白蛋白尿的糖尿病早期肾病的预防(优先):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

Introduction Diabetes 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. Methods and analysis Investigator-initiated, prospective multicentre clinical trial, with randomised double-masked placebo-controlled intervention and a prospective observational study. We aim to include 3280 type 2 diabetic participants with normoalbuminuria. The CKD273 classifier will be assessed in all participants. Participants with high-risk pattern are randomised to treatment with spironolactone 25mg once daily, or placebo, whereas, those with low-risk pattern will be observed without intervention other than standard of care. Treatment or observational period is 3years. The primary endpoint is development of confirmed microalbuminuria in 2 of 3 first morning voids urine samples. Ethics and dissemination The study will be conducted under International Conference on Harmonisation - Good clinical practice (ICH-GCP) requirements, ethical principles of Declaration of Helsinki and national laws. This first new biomarker-directed intervention trial aiming at primary prevention of diabetic nephropathy may pave the way for personalised medicine approaches in treatment of diabetes complications. Trial registration number NCT02040441; Pre-results.
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症的糖尿病患者,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。方法和分析由研究人员发起的前瞻性多中心临床试验,具有随机双盲安慰剂对照干预和一项前瞻性观察性研究。我们的目标是将3280名2型糖尿病参与者与正常白蛋白尿纳入研究。 CKD273分类器将在所有参与者中进行评估。高风险模式的参与者被随机分配到每天一次接受25mg螺内酯或安慰剂的治疗,而低风险模式的参与者将在没有护理标准干预的情况下进行干预。治疗或观察期为3年。主要终点是3个第一个早晨尿样中的2个尿样中有2个证实为微量白蛋白尿。道德与传播该研究将在国际协调会议-良好临床实践(ICH-GCP)要求,赫尔辛基宣言的道德原则和国家法律的指导下进行。这项旨在针对糖尿病肾病的一级预防的新的以生物标志物为导向的干预试验可能为个性化药物治疗糖尿病并发症铺平了道路。试用注册号NCT02040441;结果。

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