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血管紧张素I转换酶基因多态性与II型糖尿病中的糖尿病肾病

Angiotensin I converting enzyme gene polymorphism and diabetic nephropathy in type II diabetes.

作者信息

Schmidt S, Ritz E

机构信息

Department of Internal Medicine, Ruperto-Carola University of Heidelberg, Germany.

出版信息

Nephrol Dial Transplant. 1997;12 Suppl 2:37-41.

PMID:9269698
Abstract

BACKGROUND

The factors leading to diabetic nephropathy (DN) are not completely understood. Besides glycaemic control, genetic predisposition seems to play an important role for the development of DN. Genes of the renin-angiotensin system are potential candidate genes. An insertion/deletion polymorphism in the gene coding for the angiotensin I converting enzyme (ACE) has been extensively examined, but results were conflicting.

METHODS

We studied 658 patients with type II diabetes (n = 347 without DN, n = 311 with DN).

RESULTS

No difference was found in genotype distribution or allele frequencies between diabetic patients with and without nephropathy as defined by albumin excretion > or = 30 mg/day, but patients on dialysis had more frequently the DD-genotype.

CONCLUSION

Although we acknowledge certain problems in the design of the study the results in this large cohort suggest that the I/D polymorphism of the ACE gene does not play a major role in the development of DN. They are compatible, however, with a role of the gene in progression.

摘要

背景

导致糖尿病肾病(DN)的因素尚未完全明确。除血糖控制外,遗传易感性似乎在DN的发生发展中起重要作用。肾素 - 血管紧张素系统的基因是潜在的候选基因。血管紧张素I转换酶(ACE)编码基因中的插入/缺失多态性已被广泛研究,但结果相互矛盾。

方法

我们研究了658例II型糖尿病患者(n = 347例无DN,n = 311例有DN)。

结果

根据白蛋白排泄量≥30mg/天定义,有肾病和无肾病的糖尿病患者在基因型分布或等位基因频率上未发现差异,但透析患者中DD基因型更为常见。

结论

尽管我们承认本研究设计存在某些问题,但在这个大型队列中的结果表明,ACE基因的I/D多态性在DN的发生中不发挥主要作用。然而,这些结果与该基因在疾病进展中的作用是相符的。

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