2014
DOI: 10.1517/13543784.2014.892580
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Have we reached the limits for the treatment of diabetic nephropathy?

Abstract: Although issues around validity of surrogate markers and clinical end points have complicated trial data in the field, currently available evidence is not persuasive as regards the clinical application of these agents. There remains a clear and growing need for emerging therapeutics to be used in combination with RAAS blocking agents.

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Cited by 22 publications
(14 citation statements)
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“…Treatment regimens commonly include RAAS-blocking agents such as angiotensin-converting enzyme (ACE) inhibitors or angiotensin II receptor blockers (ARB). However, these therapies are considered to be inadequate for the treatment of diabetic nephropathy, as they do not reverse the disease [9, 10]. Treatment combinations, such as dual-RAAS blockade with ACE inhibitors and ARBs, have been considered, but they are associated with adverse events (e.g., hyperkalemia and acute kidney injury); thus, these treatment combinations are not recommended, and are contraindicated in patients with renal impairment [8, 11].…”
Section: Introductionmentioning
confidence: 99%
“…Treatment regimens commonly include RAAS-blocking agents such as angiotensin-converting enzyme (ACE) inhibitors or angiotensin II receptor blockers (ARB). However, these therapies are considered to be inadequate for the treatment of diabetic nephropathy, as they do not reverse the disease [9, 10]. Treatment combinations, such as dual-RAAS blockade with ACE inhibitors and ARBs, have been considered, but they are associated with adverse events (e.g., hyperkalemia and acute kidney injury); thus, these treatment combinations are not recommended, and are contraindicated in patients with renal impairment [8, 11].…”
Section: Introductionmentioning
confidence: 99%
“…However, clinical data show that intensive glycemic and hypertension control has limited therapeutic effectiveness for DN (Parving et al, 2012;Fried et al, 2013;Gentile et al, 2014;Hajhosseiny et al, 2014). Additional studies are also needed to determine if AC261 can reverse renal damage associated with DN since in this work we are measuring the ability of the drug to inhibit the development of DN.…”
Section: Downloaded Frommentioning
confidence: 99%
“…AGEs 的异常积累是 DPN 发生发展的重要病理机制 [9] , 甚至在糖尿病 的各种并发症患者中均发现了 AGEs 水平的升高 [10] ,长期高血糖可使周围神经的结构和功能蛋白发生糖基 化,生成更多 AGEs,AGEs 与特定的受体结合,导致一系列神经功能障碍。吡哆胺作为维生素 B 6 的天然 成分,可以抑制 AGEs 的生成,有着治疗糖尿病肾病和 DPN 的广阔前景 [11] 。同时,研究者发现一些常用药 物也有抑制 AGEs 的作用,如阿卡波糖、二甲双胍、维生素 C、替尼西坦等 [12] 。…”
Section: 高级糖基化产物(Ages)抑制药unclassified