Lepedda Antonio Junior, De Muro Pierina, Capobianco Giampiero, Formato Marilena
Department of Biomedical Sciences, University of Sassari, Via Muroni 25, 07100, Sassari, Italy.
Gynecologic and Obstetric Clinic, Department of Surgical, Microsurgical and Medical Sciences, University of Sassari, Viale San Pietro 12, 07100, Sassari, Italy.
J Diabetes Complications. 2017 Jan;31(1):149-155. doi: 10.1016/j.jdiacomp.2016.10.013. Epub 2016 Oct 17.
Because of the high incidence of kidney disease in diabetic patients, the early diagnosis of renal impairment is a key point for intervention and management. Although urinary albumin excretion currently represents the accepted standard to assess both diabetic nephropathy and cardiovascular risk, it has some limitations as structural changes in the glomerular basement membrane may occur before the onset of microalbuminuria. It is therefore important to identify urinary markers that may provide greater sensitivity, earlier detection, and greater predictive power for diabetes complications. In this respect, urinary glycosaminoglycans/proteoglycans (GAGs/PGs) have been long associated with several kidney diseases as well as diabetic nephropathies as their levels increase more readily than albuminuria. In particular, heparan sulfate, a key component of the glomerular basement membrane responsible for its charge-dependent permeability, is excreted into urine at higher concentrations during the early kidney remodeling events caused by the altered glucose metabolism in diabetes. Over the past few years, also urinary trypsin inhibitor has been linked to a chronic inflammatory condition in both type 1 and 2 diabetes. The underlying mechanisms of such increase are not completely known since either a systemic inflammatory condition or a more localized early renal impairment could play a role. Nevertheless, the association with other inflammatory markers and a detailed urinary trypsin inhibitor structural characterization in diabetes remain to be elucidated. This review will discuss a great deal of information on the association between urinary GAGs/PGs and type 1 and 2 diabetes, with particular emphasis on renal involvement, and their potential as markers useful in screening, diagnosis and follow up to be associated with the current standard tests.
由于糖尿病患者肾病的高发病率,早期诊断肾功能损害是干预和管理的关键。尽管目前尿白蛋白排泄是评估糖尿病肾病和心血管风险的公认标准,但它存在一些局限性,因为肾小球基底膜的结构变化可能在微量白蛋白尿出现之前就已发生。因此,识别可能对糖尿病并发症具有更高敏感性、更早检测和更强预测能力的尿液标志物非常重要。在这方面,尿糖胺聚糖/蛋白聚糖(GAGs/PGs)长期以来一直与几种肾脏疾病以及糖尿病肾病相关,因为它们的水平比蛋白尿更容易升高。特别是硫酸乙酰肝素,作为肾小球基底膜负责其电荷依赖性通透性的关键成分,在糖尿病患者葡萄糖代谢改变引起的早期肾脏重塑过程中,会以更高的浓度排泄到尿液中。在过去几年中,尿胰蛋白酶抑制剂也与1型和2型糖尿病的慢性炎症状态有关。这种升高的潜在机制尚不完全清楚,因为全身性炎症状态或更局部的早期肾功能损害都可能起作用。然而,与其他炎症标志物的关联以及糖尿病患者尿胰蛋白酶抑制剂的详细结构特征仍有待阐明。本综述将讨论大量关于尿GAGs/PGs与1型和2型糖尿病之间关联的信息,特别强调肾脏受累情况,以及它们作为与当前标准检测相关的筛查、诊断和随访有用标志物的潜力。