Abstract
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, β3-adrenergic receptor gene, hemochromatosis, and α2β1 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.
Key words
Type 2 diabetes - polymorphism - quantitative trait - review - association
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Prof. Dr. med. Ralf Paschke
University of Leipzig
Department of Endocrinology and Diabetes
Philipp-Rosenthal-Straße 27
04103 Leipzig
Germany
Phone: + 49 (341) 971-32 00
Fax: + 49 (341) 971-32 09
Email: Ralf.Paschke@medizin.uni-leipzig.de