Liu Yongmei, Freedman Barry I
Department of Internal Medicine/Nephrology, Wake Forest University School of Medicine, Winston-Salem, North Carolina 27157-1053, USA.
Kidney Int Suppl. 2005 Dec(99):S94-7. doi: 10.1111/j.1523-1755.2005.09917.x.
Diabetic kidney disease is a microvascular complication that is observed in a minority of patients with long-standing hyperglycemia. Diabetic nephropathy (DN) is associated with shortened patient survival, severe morbidity, and increased health care costs. Unfortunately, the incidence rates of DN continue to increase in Western societies, and DN is now the most common reported cause of end-stage renal disease in developed nations. DN results from a complex interplay between inherited and environmental factors. This article reviews the data that support an inherited basis for susceptibility to DN by summarizing familial aggregation studies, genome-wide linkage, and population-based association analyses in diabetic and nondiabetic kidney disease. Recent evidence linking genes involved in the regulation of endothelial function with genetic predisposition to albuminuria is presented. The integration of carefully designed genetic linkage and association studies with gene expression experiments in human and animal models of diabetic kidney disease appear to offer great promise for detecting the molecular mechanisms underlying susceptibility to DN.
糖尿病肾病是一种微血管并发症,在少数长期高血糖患者中可见。糖尿病肾病(DN)与患者生存期缩短、严重发病及医疗费用增加相关。不幸的是,在西方社会,DN的发病率持续上升,目前在发达国家,DN是终末期肾病最常见的报告病因。DN是遗传因素与环境因素复杂相互作用的结果。本文通过总结糖尿病和非糖尿病肾病的家族聚集性研究、全基因组连锁分析及基于人群的关联分析,回顾支持DN易感性存在遗传基础的数据。文中还介绍了将参与内皮功能调节的基因与蛋白尿遗传易感性联系起来的最新证据。在糖尿病肾病的人类和动物模型中,精心设计的遗传连锁和关联研究与基因表达实验相结合,似乎为检测DN易感性的分子机制带来了巨大希望。