Journal of the Korean Ophthalmological Society 2005;46(11):1911-1918.
Published online November 30, 2005.
Single Nucleotide Polymorphisms in the 3'-Untranslated Region of Vascular Endothelial Growth Factor in Diabetic Retinopathy.
Suk Ho Byeon, Hyun Sub Oh, Bo Young Ahn, Sun Pyo Hong, Jin Kook Kim, Oh Woong Kwon
1Institute of Vision Research, Department of Ophthalmology, Yonsei University, College of Medicine, Seoul, Korea. owkwon0301@yumc.yonsei.ac.kr
2R and D Center, EyeGene Inc, Seoul, Korea.
3Genematrix, Seoul, Korea.
4BS Eye Center, Seoul, Korea.
한국인의 혈관내피성장인자 3’ 비번역 부위의 유전자 다형성과 당뇨망막증과의 상관성
변석호1,오현섭1,안보영2,홍선표3,김진국4,권오웅1
Institute of Vision Research, Department of Ophthalmology, Yonsei University, College of Medicine1, Seoul, Korea R&D Center, EyeGene Inc2, Seoul, Korea, Genematrix3, Seoul, Korea, BS Eye Center4, Seoul, Korea
Correspondence:  Suk-Ho Byeon, M.D.1
Abstract
PURPOSE
Recent studies suggest that increased expression of the vascular endothelial growth factor (VEGF) may play a role in the pathogenesis of diabetic complications. The aim of this study was to assess the potential association of VEGF gene polymorphisms with disease expression of retinopathy in patients with diabetes mellitus. METHODS: We studied 96 diabetic patients to determine whether there is an association between diabetic retinopathy in VEGF and VEGFR gene; all patients were unrelated Korean individuals (PDR, n=32; NPDR, n=25; no DMR, n=39). We analyzed VEGF and VEGFR SNP by restriction fragment mass polymorphism (RFMP). PCR was performed with primers designed to introduce a type IIS restriction endonuclease recognition sequence (FokI, BstF5I) ahead of the polymorphism site. The enzymatic cleavage of the products resulted to excision of two oligonucleotide fragments containing the variation site, and then masses of the resulting oligonucleotide fragments were examined by matrix assisted laser desorption time of flight mass spectrometry (MALDI-TOF MS). Difference are seen as the presence, absence, or mass change in peaks corresponding to the fragments affected by existence of polymorphism that have base substitution at the site of variation. RESULTS: We found that the genotype frequencies of two polymorphisms shown to be completely linked to each other (rs3025039; vf1, rs3025040; vf2) and one polymorphism (rs3812867; vfr1) within 3'-untranslated regions (3'-UTR) of the VEGF and VEGFR1 significantly differed between patients with and without retinopathy. The frequencies of the vf1, vf2 and vfr1 did not differ significantly between the NPDR and PDR group CONCLUSIONS: These data implicate the polymorphisms in the 3'-UTR of the VEGF and VEGFR1 genes as risk factors for diabetic retinopathy.
Key Words: Diabetic retinopathy;MALDI-TOF MS;RFMP;SNP;VEGF


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