Uhlmann K, Kovacs P, Boettcher Y, Hammes H-P, Paschke R
Department of Endocrinology and Diabetes, University of Leipzig, Leipzig, Germany.
Exp Clin Endocrinol Diabetes. 2006 Jun;114(6):275-94. doi: 10.1055/s-2006-924260.
Familial aggregation as well as racial and ethnic differences in incidence suggest that genetic components play a role in the development of diabetic retinopathy (DR), several approaches have been used to identify genes contributing to the development of retinopathy. We searched the literature database using the keywords [diabetes], [gene], for publications dealing with retinopathy. 88 original publications reporting data on genetics of retinopathy were found. For the purpose of this review, a simple scoring system was applied, that results in a score for each considered gene to indicate its potential relevance in genetic control of retinopathy. Based on published studies, the most intriguing genes for further genetic studies are aldose receptor, advanced glycation end products receptor, vascular endothelial growth factor, intercellular adhesion molecule 1, beta3-adrenergic receptor gene, hemochromatosis, and alpha2beta1 integrin. Pathways involving these gene products may represent a fruitful area for further studies aimed at investigating the genetics and pathophysiology of DR. Meta-analyses of candidate gene studies may provide further useful insights into their role. In addition, our paper addresses several issues challenging genetic studies of retinopathy such as replication of associations, patient ascertainment schemes, or accurately defined phenotypes.
家族聚集现象以及发病率的种族和民族差异表明,遗传因素在糖尿病视网膜病变(DR)的发生发展中起作用,已经采用了几种方法来鉴定导致视网膜病变发生的基因。我们使用关键词[糖尿病]、[基因]在文献数据库中搜索有关视网膜病变的出版物。共找到88篇报告视网膜病变遗传学数据的原始出版物。为了本综述的目的,应用了一个简单的评分系统,该系统为每个被考虑的基因给出一个分数,以表明其在视网膜病变遗传控制中的潜在相关性。基于已发表的研究,进一步进行基因研究最具吸引力的基因是醛糖还原酶、晚期糖基化终末产物受体、血管内皮生长因子、细胞间黏附分子1、β3-肾上腺素能受体基因、血色素沉着症和α2β1整合素。涉及这些基因产物的信号通路可能是进一步研究糖尿病视网膜病变遗传学和病理生理学的一个富有成果的领域。候选基因研究的荟萃分析可能会为它们的作用提供进一步有用的见解。此外,我们的论文还讨论了糖尿病视网膜病变基因研究面临的几个问题,如关联的重复性、患者确定方案或精确界定的表型。