期刊文献+

非微小病变型肾病综合征患儿脂质紊乱及载脂蛋白E基因的研究 被引量:1

The hyper lipidemia and apolipoprotein E gene in the children with with no-minimal change glomerulopathy of primary nephrotic syndrome
下载PDF
导出
摘要 目的 研究非微小病变型肾病综合征患儿脂质紊乱及载脂蛋白E基因,为临床上正确选择合适的病例进行降脂治疗提供依据。方法 用酶法测定了50例非微小病变型(NMCD)患儿及80例健康儿童血脂、脂蛋白、载脂蛋白三个水平共七个脂质代谢指标,用PCR-SSCP法测定了研究对象载脂蛋白E(ApoE)基因型,并行肾穿刺活检术检查NS患儿病理类型。结果 临床表现为难治性肾病综合征的NMCD患儿存在明显脂质紊乱(P<0.01),随诊半年后仍有绝大多数NMCD患儿存在明显脂质紊乱。NMCD组ApoE2等位基因显著高于健康儿童(11.00%vs5.00%,P<0.05)。结论 NMCD患儿脂质紊乱持续的时间较长,这类患儿,尤其携ApoE_2等位基因者,更易发生进行性肾脏损害,动脉粥样硬化及冠心病。 Objective To study the hyperlipidemia and apolipoprotein E gene in the children with no-minimal change glomerulopathy of primary nephrotic syndrome (NS). Method 50 children with no-minimal change glomerulopathy( NMCN group, the clinical type was steroid-resistent NS) were observed group, 80 age and sex-matched healthy children were control group. 7 Lipoprotein metabolism parameters including serum total-cholesterol(TC), triglyceride(TG), high-density lipoprotein cholesterol(HDL-C), low-density lipoprotein cholesterol (LDL-C), apolipoprotein AI(ApoAI), apolipoprotein B (ApoB), lipoprotein (a) [Lp(a)]were detected by enzyme method and Single-strand conformational polymorphism (PCR - SSCP) was used to determine the ApoE genotypes in 2 groups. Results Serum TC, TG, HDL-C, LDL-C, ApoAI, ApoB, Lp(a) in two observed group were highter than healthy cotrols significantly (P<0.01). After treated by prednison, The incidence of abnormal lipoprotein metabolism parameters in observed group were higher than those in the cotrol group significantly (P<0.01), After 6 month, the abnormal incidence of Serum TC, TG, LDL-C, ApoB, Lp (a)were 80.00 % , 76. 67 % , 83. 33 % , 87. 67 % , 76. 67 % respectively in 30 cases. the ApoE2 allele gene frequence in observed group is highter than healthy cotrols significantly (P<0.05) .Conclusion There had been obvions and long time ahnomilities of serum lipoprotein metabolism parameters in the children with no-minimal change glomerulopathy of primary nephrotic syndrome, the ApoE2 allele gene frequence is highter in those cases. There are the risk facters of suffering from atherosclerosis and cardiovascular diseases in those cases. The lipids-reduced drugs should be considered use in those cases.
出处 《中国中西医结合肾病杂志》 2000年第1期25-27,共3页 Chinese Journal of Integrated Traditional and Western Nephrology
基金 广东卫生科技基金(项目编号 B1999150)
关键词 肾病综合征 高脂血症 肾脏病理 基因多态性 nephrotic syndrome hyperlipidemia renal pathology gene polymorphism
  • 相关文献

参考文献10

  • 1CuevasA,MaizA,ArteagaA,etal.Lipiddisordersandcardiovascularrisksinnephrology.NephrolDialTransplant.1998;13Supp14:30~3ShahSH,ShahN,SchoenemanMJ.Nephroticsyndromeandcholelithiasis.ClinPediatrPhila.1999;38(12):743~5
  • 2CuevasA,MaiA,ArteagaA,etal.Dyslipidemiasinrenaldiseases:pathogenesisandtreatment.RevMedChil.1998;126(3):315~21
  • 3QuerfeldU.Shouldhyperlipidemiainchildrenwiththenephroticsyndromebetreated?PediatrNephrol.1999;13(1):77~84
  • 4TsaiMY,SuessP,Schwichtenbergk,etal.DeterminationofapolipoproteinEgenotypesbysingle-strandconformationalpolymorphism.ClinChem.1993;39:2121~4
  • 5ShahSH,ShahN,SchoenemanMJ.Nephroticsyndromeandcholelithiasis.ClinPediatrPhila.1999;38(12):743~5
  • 6AttmanPO,SamuelssonO,AlaupovicP,etal.Lipidabnormalitiesinprogressiverenalinsufficiency.ContribNephrol.1997;120:1~10
  • 7JovenJ,VilellaE.Theinfluenceofapoproteinepsilon2homozygosityonnephrotichyperlipidemia.ClinNephrol.1997Sep,48(3):141~5
  • 8姜傥.脂蛋白肾病:一种新型的与脂类代谢相关的肾小球疾病[J].中华肾脏病杂志,1997,13(3):179-182. 被引量:10
  • 9曾华松,刘绪青.载脂蛋白E遗传多态性与脂蛋白肾病[J].中华肾脏病杂志,1998,14(1):60-61. 被引量:4
  • 10姜傥,许乃贵,邹万忠,黄锋先,关伟明,吴义方,李鵕,董秀清.脂蛋白肾病—一种新型的肾小球疾病伴进行性硬化[J].中华肾脏病杂志,1997,13(3):134-136. 被引量:18

二级参考文献2

  • 1Zhang P,Am J Kidney Dis,1994年,24卷,942页
  • 2J. J. Martin,J. G. Leroy,M. Eygen,C. Ceuterick. I-cell disease[J] 1984,Acta Neuropathologica(3):234~242

共引文献26

同被引文献9

引证文献1

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部