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肾病综合征患者的脂蛋白(a):免疫抑制和蛋白尿的影响

Lipoprotein(a) in patients with the nephrotic syndrome: influence of immunosuppression and proteinuria.

作者信息

Wanner C, Bartens W, Nauck M, Zäuner I, Greiber S, Schollmeyer P

机构信息

Department of Medicine, University of Freiburg, Germany.

出版信息

Miner Electrolyte Metab. 1996;22(1-3):26-30.

PMID:8676820
Abstract

Lipoprotein(a) [Lp(a)] is a plasma lipoprotein whose structure and composition closely resemble that of low-density lipoproteins, but contains an additional protein called apolipoprotein(a) [apo(a)]. Factors which modulate plasma Lp(a) concentrations are poorly understood. The influence of nephrotic syndrome on Lp(a) levels was investigated in 103 patients with nephrotic syndrome: 72 with primary kidney disease and 31 with diabetic nephropathy. Nephrotic patients had significantly higher Lp(a) levels (mean 63 +/- 7 mg/dl; median 42 mg/dl) compared with controls (mean 22 +/- 2 mg/dl; median 8 mg/dl). Fifty-seven percent of the patients and 22% of the controls had values greater than 30 mg/dl. Within all apo(a) isoform classes, higher concentrations of Lp(a) were seen in the nephrotic patients compared with controls. In 17 patients with primary kidney disease remission of the nephrotic syndrome was induced by immunosuppressive treatment and Lp(a) concentration dropped in parallel with the reduction of proteinuria (pretreatment mean, 98 +/- 9 mg/dl vs. remission mean, 25 +/- 5 mg/dl). In 9 patients where multiple measurements were done, multiple regression analysis showed a strong relation of Lp(a) with the amount of proteinuria (p < 0.01). We conclude that most patients with the nephrotic syndrome have Lp(a) concentrations which are substantially elevated compared with control subjects of the same apo(a) isoform. Because Lp(a) concentrations are substantially reduced when remission of the nephrotic syndrome is induced by immunosuppressive drugs, it is likely that nephrotic syndrome directly results in elevation of Lp(a). The high levels of Lp(a) in nephrotic syndrome could potentially cause glomerular injury as well as increase the risk of atherosclerosis and thrombotic events associated with this disorder.

摘要

脂蛋白(a)[Lp(a)]是一种血浆脂蛋白,其结构和组成与低密度脂蛋白极为相似,但还含有一种名为载脂蛋白(a)[apo(a)]的额外蛋白质。目前对调节血浆Lp(a)浓度的因素了解甚少。我们对103例肾病综合征患者(72例原发性肾病患者和31例糖尿病肾病患者)进行了肾病综合征对Lp(a)水平影响的研究。与对照组(平均22±2mg/dl;中位数8mg/dl)相比,肾病患者的Lp(a)水平显著更高(平均63±7mg/dl;中位数42mg/dl)。57%的患者和22%的对照组Lp(a)值大于30mg/dl。在所有apo(a)异构体类别中,与对照组相比,肾病患者的Lp(a)浓度更高。在17例原发性肾病患者中,免疫抑制治疗诱导了肾病综合征缓解,Lp(a)浓度随蛋白尿减少而平行下降(治疗前平均98±9mg/dl,缓解时平均25±5mg/dl)。在9例进行了多次测量的患者中,多元回归分析显示Lp(a)与蛋白尿量之间存在密切关系(p<0.01)。我们得出结论,大多数肾病综合征患者的Lp(a)浓度与相同apo(a)异构体的对照受试者相比大幅升高。由于免疫抑制药物诱导肾病综合征缓解时Lp(a)浓度大幅降低,肾病综合征很可能直接导致Lp(a)升高。肾病综合征中高水平的Lp(a)可能会导致肾小球损伤,并增加与该疾病相关的动脉粥样硬化和血栓形成事件的风险。

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