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Plasma level and genetic variation of apolipoprotein E in patients with lipoprotein glomerulopathy

机译:脂蛋白性肾小球病患者血浆载脂蛋白E水平和遗传变异

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Background Lipoprotein glomerulopathy (LPG) is a renal disease characterized by thrombus-like lipoproteins in the glomerular capillaries and its abnormal lipoprotein profiles with marked elevation of apolipoprotein E (apoE). In this study, 15 Chinese patients with LPG were involed in exploring the association of the genetic variation and its plasma level in the pathogenesis of LPG. Methods A retrospective analysis of the clinical and pathological features was made in 15 patients with LPG. Plasma concentrations of apoE were measured with radial immunodiffusion assay. Genetic variations of apoE gene were detected using polymerase chain reaction and restriction fragment length polymorphism. Glomerular deposition of apoA, apoB and apoE in these patients were detected by immunofluorescence staining using monoclonal antibodies. Results Biochemical profiles of lipids and lipoproteins revealed markedly elevated levels of triglyceride, apoB and apoE, but approximately normal levels of total cholesterol, apoA1 and lipoprotein(a) [Lp(a)] , which resembled familial hypertriglyceridemia. Genetic analysis demonstrated that the genotype distribution of apoE were 7 cases with ε3/ε 4, 4 cases with ε3/ε 3 and 2 cases with ε2/ε 3. The other 2 cases (a mother and her son) showed a same distinct band. The band pattern of later 2 cases was quite similar to the apoE variant of Tokyo type. The calculated allele frequency of ε 4 was relatively high in cases with LPG in comparison with that in the normal controls. We further divided the 13 patients into three groups according to their genotypes of apoE. Patients with the genotype of apoE ε2/ε3 showed a lower level of plasma apoE as compared to those with apoE ε3/ε4 (P < 0. 05). The serum level of high-density lipoprotein ( HDL) was the lowest in patients with the genotype of apoE ε3/ε4. No difference was found among the patients with different apoE genotype in the other clinical and pathological characteristics. Conclusions The genotype of apoE ε3/ε4 is the predominant one in Chinese patients with LPG. Patients with this genotype tend to have a higher plasma level of apoE and more severe lipid dysmetabolism. No correlation was found between the genotype of apoE and the clinical features in patients with LPG.
机译:背景脂蛋白肾小球病(LPG)是一种肾脏疾病,其特征在于肾小球毛细血管中的血栓样脂蛋白及其异常脂蛋白谱,其中载脂蛋白E(apoE)明显升高。在这项研究中,有15名中国LPG患者参与了探讨LPG发病机理中遗传变异及其血浆水平的关联。方法对15例LPG患者的临床和病理特点进行回顾性分析。用放射免疫扩散测定法测量血浆apoE的浓度。使用聚合酶链反应和限制性片段长度多态性检测apoE基因的遗传变异。使用单克隆抗体通过免疫荧光染色检测这些患者的肾小球apoA,apoB和apoE沉积。结果脂质和脂蛋白的生化特征显示甘油三酯,apoB和apoE的水平显着升高,但总胆固醇,apoA1和脂蛋白(a)[Lp(a)]的水平接近正常水平,类似于家族性高甘油三酯血症。遗传分析表明,apoE的基因型分布为ε3/ε4的7例,ε3/ε3的4例,ε2/ε3的2例。其他2例(母亲和儿子)显示相同的明显条带。后两个案例的带模式与东京型的apoE变体非常相似。与正常对照组相比,LPG患者的ε4等位基因频率计算值相对较高。根据他们的apoE基因型,我们将13名患者进一步分为三组。与apoEε3/ε4基因型的患者相比,apoEε2/ε3基因型的患者血浆apoE水平较低(P <0. 05)。基因型apoEε3/ε4的患者血清高密度脂蛋白(HDL)水平最低。在其他apoE基因型不同的患者之间,在其他临床和病理特征上均未发现差异。结论apoEε3/ε4基因型是中国LPG患者的主要基因型。具有这种基因型的患者倾向于具有更高的apoE血浆水平和更严重的脂质代谢异常。 LPG患者的apoE基因型与临床特征之间没有相关性。

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