Cao Zemin, Cooper Mark E
Diabetic Complications Division, Baker IDI Heart and Diabetes Institute, and Department of Immunology, Monash University, AMREP, Melbourne, Victoria, Australia.
J Diabetes Investig. 2011 Aug 2;2(4):243-7. doi: 10.1111/j.2040-1124.2011.00131.x.
As the increasing prevalence of diabetes reaches epidemic proportions worldwide, diabetic nephropathy and associated end-stage renal failure will be an unavoidable major health burden to not only individuals with diabetes and their families, but also to the health systems both in developed and developing countries. Over the past decade, a large body of research has focused on diabetic nephropathy ranging from studies in molecular signaling, hemodynamic regulation and pharmaceutical intervention to clinical outcomes. It is likely that the pathophysiology of diabetic nephropathy involves a multifactorial interaction between metabolic and hemodynamic factors. Metabolic factors involve glucose-dependent pathways, such as advanced glycation end-products and their receptors. Hemodynamic factors include various vasoactive hormones, such as components of the renin-angiotensin system. It is likely that these metabolic and hemodynamic factors interact through shared molecular and signaling pathways, such as nuclear factor kappa-light-chain-enhancer of activated B cells and protein kinase C with associated reactive oxygen species generation. It is likely that these contributing factors cause pathological damage not only to the glomerulus, in particular podocytes, but also to the tubulointerstitium. Specific inhibitors of the various pathways are now available and these emerging pharmaceutical interventions might have potential implications for the prevention and treatment of diabetic nephropathy. The mainstay of therapy remains the achievement of optimal glycemic and blood pressure control in order to slow the progression of diabetic nephropathy. Agents that interrupt the renin-angiotensin system have been shown to be particularly useful as renoprotective agents in both hypertensive and normotensive type 1 and type 2 diabetic subjects. (J Diabetes Invest, doi: 10.1111/j.2040-1124.2011.00131.x, 2011).
随着糖尿病在全球的患病率不断上升,已达到流行程度,糖尿病肾病及相关的终末期肾衰竭不仅将成为糖尿病患者及其家庭不可避免的重大健康负担,也会给发达国家和发展中国家的卫生系统带来负担。在过去十年中,大量研究聚焦于糖尿病肾病,涵盖从分子信号传导、血流动力学调节及药物干预到临床结局等方面。糖尿病肾病的病理生理学可能涉及代谢和血流动力学因素之间的多因素相互作用。代谢因素包括葡萄糖依赖性途径,如晚期糖基化终产物及其受体。血流动力学因素包括各种血管活性激素,如肾素 - 血管紧张素系统的组成部分。这些代谢和血流动力学因素可能通过共享的分子和信号传导途径相互作用,如活化B细胞的核因子κB轻链增强子和蛋白激酶C以及相关的活性氧生成。这些促成因素可能不仅对肾小球,特别是足细胞,而且对肾小管间质造成病理损害。现在已有各种途径的特异性抑制剂,这些新出现的药物干预可能对糖尿病肾病的预防和治疗具有潜在意义。治疗的主要方法仍然是实现最佳的血糖和血压控制,以减缓糖尿病肾病的进展。已证明,在1型和2型糖尿病高血压和血压正常的患者中,阻断肾素 - 血管紧张素系统的药物作为肾脏保护剂特别有用。(《糖尿病研究杂志》,doi: 10.1111/j.2040 - 1124.2011.00131.x,2011年)