Attman P O, Samuelsson O, Alaupovic P
Department of Nephrology, University of Göteborg, Sahlgrenska University Hospital, Sweden.
Kidney Int Suppl. 1997 Dec;63:S98-101.
Plasma lipoproteins (LP) may be identified on the basis of density properties or apolipoprotein (apo) composition. ApoB-containing LP occur in VLDL, IDL and LDL. There are several types of apoB-containing LP characterized by specific composition of minor apolipoproteins (apoC, apoE etc.) and lipid constituents (triglycerides and cholesterol), metabolic properties and relative atherogenicity. The alterations of lipoprotein metabolism in renal disease resulting in elevated levels of apoB-containing LP may be reflected in hyperlipidemia. Whereas nephrotic syndrome and heavy proteinuria are associated with increased formation of cholesterol-rich apoB-containing LP in LDL and VLDL, the characteristic feature in renal failure is the accumulation of intact or partially metabolised triglyceride-rich LP in IDL and VLDL. The potentially atherogenic apoB-containing LP have been linked to the pathogenic processes that result in progressive glomerular and interstitial lesions and ultimate loss of renal function. The mechanisms of injury are not fully understood. Receptor- and non-receptor mediated uptake of LP by mesangial cells may induce or accelerate proliferative and sclerotic processes in the glomerular mesangium that are analogous to atherosclerosis in the arterial wall. Changes in glomerular permeability can result in increased filtration of LP that may be internalized by tubular cells and elicit corresponding lesions in the interstitial tissues. The negative impact of proteinuria on the prognosis of renal disease could be mediated in part through an increased filtration of lipoproteins. Induction of hyperlipidemia accelerates glomerular and interstitial damage in experimental renal failure. This can be attenuated by treatment with hypolipemic agents. In patients, increased concentrations of apoB-containing LP are associated with more rapid progression of renal insufficiency in both primary renal disease and diabetic nephropathy. It is, however, presently not known to what extent treatment of the renal dyslipidemia can modify the progression of chronic renal failure. Experimental and clinical evidence suggest that apoB-containing LP may play a pathogenetic role in the progression of renal disease.
血浆脂蛋白(LP)可根据密度特性或载脂蛋白(apo)组成来识别。含载脂蛋白B的LP存在于极低密度脂蛋白(VLDL)、中间密度脂蛋白(IDL)和低密度脂蛋白(LDL)中。有几种含载脂蛋白B的LP,其特征在于次要载脂蛋白(apoC、apoE等)和脂质成分(甘油三酯和胆固醇)的特定组成、代谢特性和相对动脉粥样硬化性。肾病中脂蛋白代谢的改变导致含载脂蛋白B的LP水平升高,这可能反映在高脂血症中。肾病综合征和大量蛋白尿与LDL和VLDL中富含胆固醇的含载脂蛋白B的LP形成增加有关,而肾衰竭的特征性表现是IDL和VLDL中完整或部分代谢的富含甘油三酯的LP积聚。具有潜在动脉粥样硬化性的含载脂蛋白B的LP与导致肾小球和间质病变进展以及最终肾功能丧失的致病过程有关。损伤机制尚未完全明了。系膜细胞通过受体介导和非受体介导摄取LP可能诱导或加速肾小球系膜中的增殖和硬化过程,这类似于动脉壁中的动脉粥样硬化。肾小球通透性的改变可导致LP滤过增加,LP可能被肾小管细胞内化并在间质组织中引发相应病变。蛋白尿对肾病预后的负面影响可能部分通过脂蛋白滤过增加来介导。高脂血症的诱导会加速实验性肾衰竭中的肾小球和间质损伤。这可以通过用降血脂药物治疗来减轻。在患者中,含载脂蛋白B的LP浓度升高与原发性肾病和糖尿病肾病中肾功能不全的更快进展相关。然而,目前尚不清楚治疗肾性血脂异常能在多大程度上改变慢性肾衰竭的进展。实验和临床证据表明,含载脂蛋白B的LP可能在肾病进展中起致病作用。