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High Risk of ESRD in Type 1 Diabetes: New Strategies Are Needed to Retard Progressive Renal Function Decline

机译:1型糖尿病ESRD的高风险:需要新的策略来延缓肾功能的持续下降

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Care of patients with type 1 diabetes (T1D) has changed during the past 30 years. Tools to control hyperglycemia have improved and it was shown that improvement in glycemic control diminished the risk of late diabetic complications, including nephropathy. Moreover, in patients with impaired renal function, aggressive treatment of hypertension and renoprotective blockade of the renin-angiotensin system were shown to postpone end-stage renal disease (ESRD), albeit for a short while. Despite these achievements, the incidence of ESRD caused by T1D in the US population has not decreased but rather has increased over the past 20 years, although it now occurs at slightly older ages. This state of affairs is a call to action. This should begin with adopting a new model of diabetic nephropathy in human beings. In that model, instead of microalbuminuria or proteinuria, the focus should be on diagnosis and treatment of progressive renal function decline that leads to ESRD. Such a model has received significant support in clinical and epidemiologic studies. Investigation of mechanisms of such progressive renal function decline should help in the identification of new therapeutic targets and the development of new interventions. To evaluate these interventions, accurate diagnostic algorithms are needed so T1D patients will be stratified according to time to onset to ESRD. Consistent with concepts of personalized medicine, the new interventions should be tailored to and evaluated in patients predicted to have rapid, moderate, or even slow progression to ESRD.
机译:在过去30年中,对1型糖尿病(T1D)患者的护理发生了变化。控制高血糖的工具已经得到改善,并且血糖控制的改善降低了晚期糖尿病并发症(包括肾病)的风险。此外,在肾功能受损的患者中,积极治疗高血压和肾素-血管紧张素系统的肾保护性阻断被证明可推迟终末期肾病(ESRD),尽管时间较短。尽管取得了这些成就,但是在过去的20年中,由T1D引起的ESRD在美国人群中的发病率并未降低,反而有所增加,尽管现在它的发生年龄略大一些。这种状况是行动的呼吁。首先应该采用一种新的人类糖尿​​病肾病模型。在该模型中,应将注意力集中在诊断和治疗导致ESRD的进行性肾功能下降,而不是微量白蛋白尿或蛋白尿。这种模型在临床和流行病学研究中得到了重要的支持。对这种进行性肾功能下降的机制进行的研究应有助于确定新的治疗靶点和开发新的干预措施。为了评估这些干预措施,需要准确的诊断算法,以便根据发病的时间将T1D患者分层。与个性化医学的概念一致,新的干预措施应针对预计可快速,中度甚至缓慢进展为ESRD的患者量身定制和评估。

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