Polimorfisme V16A Gen MnSOD pada Penderita Diabetes Melitus Tipe 2 dengan Retinopati

https://doi.org/10.22146/jtbb.16446

Tasmini Tasmini(1*), R. Haryo Yudono(2), Maliyah Madyan(3)

(1) Departement of Biochemistry, Faculty of Medicine, Public Health, and Nursing, Universitas Gadjah Mada, Yogyakarta
(2) Department of Ophthalmology, Faculty of Medicine, Public Health, and Nursing, Universitas Gadjah Mada, Yogyakarta
(3) Department of Ophthalmology, Faculty of Medicine, Public Health, and Nursing, Universitas Gadjah Mada, Yogyakarta
(*) Corresponding Author

Abstract


Complications of diabetes mellitus (DM) include diabetic retinopathy (RD) both non-proliferative diabetic retinopathy (NPDR) and proliferative diabetic retinopathy (PDR). The development of RD depends on environmental and genetic factors. MnSOD gene (manganese-superoxid dismutase) is one of the candidate risk factors gene for RD. The presence of V16A MnSOD gene polymorphism results in decrease of mitochondrial MnSOD enzymes expression and triggers the oxidative stress. Hyperglycemia in DM increases oxidative stress in tissues, including the retina resulting in metabolic abnormalities in the retina, which play a role in the development of DM complications, namely diabetic retinopathy. In Indonesia, especially the Javanese tribes in Yogyakarta, there has never been any research on MnSOD gene polymorphism in type 2 diabetes patients with and without retinopathy. Subjects were Poly Endocrine patients and Eye Polyclinic patients of Dr. Sardjito’s General Hospital, 121 subjects consisting of 63 type 2 DM patients without retinopathy were group 1 (KI) and 58 type 2 DM patients with retinopathy were group 2 (KII) (20 NPDR subjects and 38 PDR subjects). V16A polymorphism of MnSOD gene from leukocytes DNA was analyzed by PCR-RFLP method. From 121 DM subjects, 70 subjects with VV genotype were found, 50 subjects with VA genotype and 1 subject with AA genotype. From 63 non-RD DM subjects, 22 subjects with VA genotypes and 41 subjects with VV genotype were found, while in DM with retinopathy (non-PDR, n = 20) found 6 subjects with VA genotype and 14 subjects with VV genotype, and in DM with retinopathy (PDR, n = 38) found 1 subject with AA genotype, 22 subjects with VA genotype and 15 subjects with VV genotype. In DM with retinopathy (NPDR and PDR, n = 58), 1 subject was found with AA genotype, 27 subjects with VA genotype and 29 subjects with VV genotype.

Keywords


diabetes mellitus; MnSOD gene; retinopathy

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References

Abhary, S. & Burdon K.P., 2009, Diabetic retinopathy is not associated with carbonic anhydrase gene polymorphisms. Journal of Molecular Vision 15, 1179-84.

Adler, S.G., Pahl, M. & Seldin, M.F., 2000, Deciphering diabetic nephropathy: progress using genetic strategies. Journal of Curr Opin Nephrol Hypertensi 9, 99–106

Aiello, L.P. & Wong, J.S., 2000, Role of vascular endothelial growth factor in diabetic vascular complications. Journal of Kidney International 58 [Suppl 77], S113–S119

Awata, T., Inoue, K., Kurihara, S., Ohkubo, T., Watanabe, M., Inukai, K., Inoue, I. & Katayama S., 2002, Brief Genetics Report. A Common Polymorphism in the 5’-Untranslated Region of the VEGF Gene Is Associated With Diabetic Retinopathy in Type 2 Diabetes. Journal of Diabetes 51, 1635–9.

Buraczynska, M., Ksiazek, P., Baranowicz-Gaszczyk, I. & Jozwiak, L., 2006, Association of the VEGF gene polymorphism with diabetic retinopathy in type 2 diabetes patients. Journal of Nephrology Dialysis Transplant, 1-6.

De Vriese, A.S., Verbeuren, T.J., Van de Voorde, J., Lameire, N.H. & Vanhoutte, P.M., 2000, Endothelial dysfunction in diabetes. Journal of Pharmacology 130, 963–974

Fong, D.S., Aiello, L., Gardner, T.W., King, G.L., Blankenship, G., Cavallerano, J.D., Ferris, F.L. & Klein, R., 2003, Reviews. Diabetic Retinopathy. Journal of Diabetes Care 26(1), 226-229.

Guidot, D.M., McCord, J.M. & Wright, R.M., 1993, Absence of electron transport (Rho 0 state) restores growth of a manganese superoxide dismutase–deficient Saccharomyces cerevisiae in hyperoxia: evidence for electron transport as a major source of superoxide generation in vivo. Journal of Biology Chemistry 268, 26699-703.

Kiritoshi, S., Nishikawa, T. & Sonoda, K., 2003, Reactive oxygen species from mitochondria induce cyclooxgenase-2 gene expression in human mesangial cells: potential role in diabetic nephropathy. Journal of Diabetes 52, 2570-7.

Klein, R., Klein, B.E., Moss, S.E., Davis, M.D. & DeMets, D.L., 1984, The Wisconsin Epidemiologic Study of Diabetic Retinopathy. II. Prevalence and risk of diabetic retinopathy when age at diagnosis is less than 30 years. Journal of Arch Ophthalmol 102, 520–526.

Lee, S.J., Choi, M.G., Kim, D.S. & Kim, T.W., 2006, Manganese superoxide dismutase gene polymorphism (V16A) is associated with stages of albuminuria in Korean type 2 diabetic patients. Journal of Metabolism Clinical and Experimental 55, 1–7.

McIntyre, M., Bohr, D.F. & Dominiczak, A.F., 1999, Endothelial function in hypertension: the role of superoxide anion. Journal of Hypertension 34, 539-45.

Sujianto & Eko, A., 2009, Aplikasi Statistik dengan SPSS 16.0. Jakarta : Penerbit Prestasi Pustaka Publisher



DOI: https://doi.org/10.22146/jtbb.16446

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