Suppr超能文献

[2型糖尿病的候选基因与多态性分析]

[Candidate genes and polymorphism analysis in type 2 diabetes mellitus].

作者信息

Zietz Bettina, Leonhardt Katrin, Schäffler Andreas

机构信息

Innere Medizin II, Kreiskrankenhaus, Kelheim, Germany.

出版信息

Med Klin (Munich). 2006 Aug 15;101(8):605-16. doi: 10.1007/s00063-006-1090-0.

Abstract

BACKGROUND AND PURPOSE

Diabetes mellitus type 2 is a polygenic disease. Up to now, numerous candidate genes have been examined and tested for their association to metabolic parameters and late complications of diabetes. Between 2000 to 2004, polymorphisms of the following genes and their association to metabolic parameters and late complications of diabetes were examined in the authors' laboratory: PAI-1 (plasminogen activator inhibitor-1), PPARgamma2 (peroxisome proliferator-activated receptor gamma2), UCP-1 (uncoupling protein-1), and adiponectin. Based on this, the question was examined whether the combination of the respective rarely occurring genotypes results in an increased atherogenic risk and a higher prevalence of micro- and macrovascular late complications of diabetes.

MATERIAL AND METHODS

Subjects were enrolled from a cohort of 570 type 2 diabetic patients (246 female and 324 male, mean age 66.9+/-9.2 years) who had participated in a population-based study on diabetes and its complications in a mobile survey unit in 23 towns and villages in Bavaria (Germany). Retinopathy was diagnosed by nonmydriatic fundus photography (Canon CR4-45 NM). Photographs of the retina of both eyes (one photo per eye) were taken. Data on macrovascular complications of diabetes were obtained using a standardized questionnaire.

RESULTS

A significant association between the number of rarely occurring genotype combinations and the following parameters could be described: diastolic blood pressure, total cholesterol, HDL cholesterol, LDL cholesterol, triglycerides, and grade of retinopathy.

CONCLUSION

An accumulation of certain genotypes of candidate genes for diabetes mellitus type 2 is associated with the severity of dyslipidemia and microvascular late complications, e.g., grade of retinopathy. Therefore, screening for genotype combinations of these metabolic target genes might offer the opportunity to identify diabetic patients at a high risk for macro- and microvascular complications.

摘要

背景与目的

2型糖尿病是一种多基因疾病。到目前为止,众多候选基因已被检测其与糖尿病代谢参数及晚期并发症的关联。在2000年至2004年期间,作者所在实验室检测了以下基因的多态性及其与糖尿病代谢参数和晚期并发症的关联:纤溶酶原激活物抑制剂-1(PAI-1)、过氧化物酶体增殖物激活受体γ2(PPARγ2)、解偶联蛋白-1(UCP-1)和脂联素。基于此,研究了各自罕见基因型的组合是否会导致动脉粥样硬化风险增加以及糖尿病微血管和大血管晚期并发症的患病率更高。

材料与方法

研究对象来自一个包含570例2型糖尿病患者的队列(246名女性和324名男性,平均年龄66.9±9.2岁),这些患者参与了在德国巴伐利亚州23个城镇和乡村的流动调查单元中进行的一项基于人群的糖尿病及其并发症研究。通过免散瞳眼底照相(佳能CR4 - 45 NM)诊断视网膜病变。拍摄双眼视网膜照片(每只眼睛一张照片)。使用标准化问卷获取糖尿病大血管并发症的数据。

结果

可描述罕见基因型组合数量与以下参数之间存在显著关联:舒张压、总胆固醇、高密度脂蛋白胆固醇、低密度脂蛋白胆固醇、甘油三酯和视网膜病变分级。

结论

2型糖尿病候选基因的某些基因型积累与血脂异常的严重程度以及微血管晚期并发症(如视网膜病变分级)相关。因此,筛查这些代谢靶基因的基因型组合可能为识别有微血管和大血管并发症高风险的糖尿病患者提供机会。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验