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Diabetic nephropathy

机译:糖尿病肾病

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摘要

Diabetic nephropathy is the leading cause of chronic renal disease and a major cause of cardiovascular mortality. Diabetic nephropathy has been categorized into stages: microalbuminuria and macroalbuminuria. The cut-off values of micro- and macroalbuminuria are arbitrary and their values have been questioned. Subjects in the upper-normal range of albuminuria seem to be at high risk of progression to micro- or macroalbuminuria and they also had a higher blood pressure than normoalbuminuric subjects in the lower normoalbuminuria range. Diabetic nephropathy screening is made by measuring albumin in spot urine. If abnormal, it should be confirmed in two out three samples collected in a three to six-months interval. Additionally, it is recommended that glomerular filtration rate be routinely estimated for appropriate screening of nephropathy, because some patients present a decreased glomerular filtration rate when urine albumin values are in the normal range. The two main risk factors for diabetic nephropathy are hyperglycemia and arterial hypertension, but the genetic susceptibility in both type 1 and type 2 diabetes is of great importance. Other risk factors are smoking, dyslipidemia, proteinuria, glomerular hyperfiltration and dietary factors. Nephropathy is pathologically characterized in individuals with type 1 diabetes by thickening of glomerular and tubular basal membranes, with progressive mesangial expansion (diffuse or nodular) leading to progressive reduction of glomerular filtration surface. Concurrent interstitial morphological alterations and hyalinization of afferent and efferent glomerular arterioles also occur. Podocytes abnormalities also appear to be involved in the glomerulosclerosis process. In patients with type 2 diabetes, renal lesions are heterogeneous and more complex than in individuals with type 1 diabetes. Treatment of diabetic nephropathy is based on a multiple risk factor approach, and the goal is retarding the development or progression of the disease and to decrease the subject's increased risk of cardiovascular disease. Achieving the best metabolic control, treating hypertension (<130/80 mmHg) and dyslipidemia (LDL cholesterol <100 mg/dl), using drugs that block the renin-angiotensin-aldosterone system, are effective strategies for preventing the development of microalbuminuria, delaying the progression to more advanced stages of nephropathy and reducing cardiovascular mortality in patients with diabetes.
机译:糖尿病肾病是慢性肾脏疾病的主要原因,也是心血管疾病死亡的主要原因。糖尿病性肾病已分为多个阶段:微量白蛋白尿和大量白蛋白尿。微量白蛋白尿和大白蛋白尿的临界值是任意的,它们的值已受到质疑。蛋白尿正常范围较高的受试者似乎有发展为微蛋白尿或巨蛋白尿的高风险,并且其血压低于正常蛋白尿范围较低的正常白蛋白尿患者。糖尿病肾病筛查是通过测量尿样中的白蛋白来进行的。如果异常,则应在三到六个月的时间间隔内从三分之二的样本中确认。另外,建议常规评估肾小球滤过率以适当筛查肾病,因为当尿白蛋白值在正常范围内时,一些患者的肾小球滤过率降低。糖尿病肾病的两个主要危险因素是高血糖症和动脉高血压,但是1型和2型糖尿病的遗传易感性非常重要。其他危险因素是吸烟,血脂异常,蛋白尿,肾小球超滤和饮食因素。肾病在1型糖尿病患者中的病理特征是肾小球和肾小管基底膜增厚,肾小球系膜逐渐扩张(弥散性或结节状),导致肾小球滤过表面逐渐减少。同时发生传入和传出肾小球小动脉的间质形态改变和透明化。足细胞异常似乎也参与了肾小球硬化过程。在2型糖尿病患者中,肾脏病变比1型糖尿病患者异质且更为复杂。糖尿病肾病的治疗基于多危险因素方法,目的是延缓疾病的发展或进程并降低受试者罹患心血管疾病的风险。使用阻断肾素-血管紧张素-醛固酮系统的药物,实现最佳的代谢控制,治疗高血压(<130/80 mmHg)和血脂异常(LDL胆固醇<100 mg / dl),是预防微白蛋白尿发展,延缓延迟的有效策略。肾病发展至更晚期阶段,并降低糖尿病患者的心血管死亡率。

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