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Diabetes 55:2387-2391, 2006
DOI: 10.2337/db06-0021
© 2006 by the American Diabetes Association
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Brief Genetics Reports

An IGF-I Gene Polymorphism Modifies the Risk of Diabetic Retinopathy

Ingrid Rietveld1,2, M. Kamran Ikram2, Johannes R. Vingerling2,3, Albert Hofman2, Huibert A.P. Pols1,2, Steven W.J. Lamberts1, Paulus T.V.M. de Jong2,4,5, Cornelia M. van Duijn2, and Joop A.M.J.L. Janssen1

1 Department of Internal Medicine, Erasmus Medical Center, Rotterdam, the Netherlands
2 Department of Epidemiology and Biostatistics, Erasmus Medical Center, Rotterdam, the Netherlands
3 Department of Ophthalmology, Erasmus Medical Center, Rotterdam, the Netherlands
4 The Netherlands Ophthalmic Research Institute, Royal Netherlands Academy of Arts and Sciences, Amsterdam, the Netherlands
5 Department of Ophthalmology, Academic Medical Center, Amsterdam, the Netherlands

Address correspondence and reprint requests to Dr. J.A.M.J.L. Janssen, Department of Internal Medicine, Erasmus Medical Center, Room D-436, Dr. Molewaterplein 40, 3015 GD, Rotterdam, Netherlands. E-mail: j.a.m.j.l.janssen{at}erasmusmc.nl

Abbreviations: IGT, impaired glucose tolerance

The role of IGF-I in the pathogenesis of diabetic retinopathy is unclear. We studied, prospectively, the relationship between an IGF-I gene polymorphism, retinal vessel diameters, and incident diabetic retinopathy in subjects with impaired glucose tolerance (IGT) or type 2 diabetes. In all 5,505 participants of the population-based Rotterdam Study (775 with IGT, 394 with type 2 diabetes, and 4,336 control subjects), fundus color transparencies were taken at baseline (between 1990 and 1993) and at follow-up (from 1997 to 1999). The wild-type genotype (i.e., carriers of the 192- or 194-bp alleles) was present in 72.7% of the participants, while 27.3% were variant carriers. Variant carriers with IGT or type 2 diabetes appeared to have larger retinal arteriolar and venular diameters at baseline than individuals with the wild-type genotype, but these differences did not reach statistical significance. This trend was especially observed in subjects who developed retinopathy at follow-up. In variant carriers with IGT/diabetes, an increase (odds ratio 1.8 [95% CI 1.0–3.2]; P = 0.04) in the risk of retinopathy was observed compared with participants with the wild-type genotype. In conclusion, our findings suggest that this IGF-I gene polymorphism is associated with an increased risk of diabetic retinopathy.


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