Currie Gemma, McKay Gerard, Delles Christian
Gemma Currie, Christian Delles, Institute of Cardiovascular and Medical Sciences, University of Glasgow, G12 8TA Glasgow, United Kingdom.
World J Diabetes. 2014 Dec 15;5(6):763-76. doi: 10.4239/wjd.v5.i6.763.
Diabetic nephropathy (DN) is the leading cause of end stage renal disease in the Western world. Microalbuminuria (MA) is the earliest and most commonly used clinical index of DN and is independently associated with cardiovascular risk in diabetic patients. Although MA remains an essential tool for risk stratification and monitoring disease progression in DN, a number of factors have called into question its predictive power. Originally thought to be predictive of future overt DN in 80% of patients, we now know that only around 30% of microalbuminuric patients progress to overt nephropathy after 10 years of follow up. In addition, advanced structural alterations in the glomerular basement membrane may already have occurred by the time MA is clinically detectable.Evidence in recent years suggests that a significant proportion of patients with MA can revert to normoalbuminuria and the concept of nonalbuminuric DN is well-documented, reflecting the fact that patients with diabetes can demonstrate a reduction in glomerular filtration rate without progressing from normo-to MA. There is an unmet clinical need to identify biomarkers with potential for earlier diagnosis and risk stratification in DN and recent developments in this field will be the focus of this review article.
糖尿病肾病(DN)是西方世界终末期肾病的主要病因。微量白蛋白尿(MA)是DN最早且最常用的临床指标,并且与糖尿病患者的心血管风险独立相关。尽管MA仍然是DN风险分层和监测疾病进展的重要工具,但一些因素对其预测能力提出了质疑。最初认为MA能预测80%患者未来发生显性DN,而现在我们知道,经过10年随访,只有约30%的微量白蛋白尿患者会进展为显性肾病。此外,在临床上可检测到MA时,肾小球基底膜可能已经发生了晚期结构改变。近年来的证据表明,相当一部分MA患者可恢复为正常白蛋白尿,非白蛋白尿性DN的概念也有充分记录,这反映出糖尿病患者可出现肾小球滤过率降低,而无需从正常白蛋白尿进展为MA。临床上存在未满足的需求,即需要识别具有早期诊断和DN风险分层潜力的生物标志物,该领域的最新进展将是本文综述的重点。