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载脂蛋白E基因分型与糖尿病肾病风险

Apolipoprotein E genotypes and risk of diabetic nephropathy.

作者信息

Onuma T, Laffel L M, Angelico M C, Krolewski A S

机构信息

Epidemiology and Genetics Section, Joslin Diabetes Center, Boston, MA 02215, USA.

出版信息

J Am Soc Nephrol. 1996 Jul;7(7):1075-8. doi: 10.1681/ASN.V771075.

Abstract

Genetic susceptibility contributes to the development of diabetic nephropathy. In considering potentially important genetic factors, this study examined the association between genetic polymorphisms in apolipoprotein (apo) E and diabetic nephropathy in 146 patients with insulin-dependent diabetes mellitus (IDDM) of 15 to 21 years' duration. Using a case-control study design, patients with proteinuria (N = 41) (albumin excretion rate (AER) > or = 250 micrograms/min) and patients with microalbuminuria (N = 31) (AER 20 to 250 micrograms/min) were compared with patients who had normoalbuminuria (N = 74) (AER < 20 micrograms/min). Genetic polymorphisms at the apo E locus were identified by the method of denaturing gradient-gel electrophoresis. There was no significant difference in allele frequencies in the proteinuric, microalbuminuric, or normoalbuminuric groups (e2 7.3%, 9.7%, 9.5%; e3 78.1%, 72.6%, 68.2%; e4 14.6%, 17.7%, 22.3%; respectively). The distribution of the apo E genotypes among the three groups of patients was also similar. These results suggest that apo E genotypes are not associated with the development of early or advanced diabetic nephropathy in patients with IDDM.

摘要

遗传易感性在糖尿病肾病的发生发展中起作用。在考虑潜在的重要遗传因素时,本研究调查了146例病程为15至21年的胰岛素依赖型糖尿病(IDDM)患者中载脂蛋白(apo)E基因多态性与糖尿病肾病之间的关联。采用病例对照研究设计,将蛋白尿患者(N = 41)(白蛋白排泄率(AER)≥250微克/分钟)和微量白蛋白尿患者(N = 31)(AER 20至250微克/分钟)与正常白蛋白尿患者(N = 74)(AER < 20微克/分钟)进行比较。通过变性梯度凝胶电泳法鉴定apo E基因座的基因多态性。蛋白尿组、微量白蛋白尿组或正常白蛋白尿组的等位基因频率无显著差异(分别为:ε2 7.3%、9.7%、9.5%;ε3 78.1%、72.6%、68.2%;ε4 14.6%、17.7%、22.3%)。三组患者中apo E基因型的分布也相似。这些结果表明,apo E基因型与IDDM患者早期或晚期糖尿病肾病的发生无关。

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