Association between Genetic Polymorphism of Catalase (CAT) C-262T, Cu/Zn Superoxide Dismutase (SOD1) A251G and Risk of Age-related Macular Degeneration

Author
department of biology, college of sciences, Shiraz university, Shiraz, Iran
Abstract
Background: Cells have complex network of antioxidant enzymes that protect cells from induced damages by reactive oxygen species (ROS). Catalase and superoxide dismutase are known for their role as primary protection against oxidative stress. Oxidative damage is an important risk factor in age-related macular degeneration disease (AMD). For the first time in this study the impact of genetic polymorphisms of SOD1 and CAT with AMD has been examined. Hence, the association between genetic polymorphisms of catalase (CAT) C-262T, Cu/Zn superoxide dismutase (SOD1) A251G and risk of exudative AMD has been investigated. Methods: This study was carried out on blood samples collected from 112 exudative AMD patients and 112 healthy individuals. Genotyping of CAT C-262T and SOD1A251G was done by polymerase chain reaction and restriction fragment length polymorphism (PCR-RFLP) method. Differences in the frequencies were estimated using the χ2 test and risk was estimated with a logistic regression after adjusting for smoking, working place and age status. Results: There was significant difference between CAT CT+TT genotype and AMD disease (P=0.009, OR=0.38, 95%CI=0.18-0.78). Also T-allele has a significant association with risk of AMD and decreases risk of disease (P=0.036, OR=0.59, 95%CI=0.36-0.96), but there was no significant differences between SOD1A251G and variant homozygous and heterozygous frequencies in patients compared to controls (P=0.589, OR=0.77, 95%CI=0.3-1.96). Conclusions: The data presented suggest that the T-allele in CAT genotypes can increase catalase expression and activity, as a result of which generation of reactive oxygen species (ROS) can be decreased. Therefore it is suggested that increased expression of CAT as a result of T-allele in CAT genotypes and existence of T-allele in CAT genotypes is associated with decreased risk of AMD.

Keywords


[1]     Arsova-Sarafinovska1y Z, Matevska N, Petrovski D, Banev S, Dzikova S, et al. 2008. Manganese superoxide dismutase (MnSOD) genetic polymorphism is associated with risk of early-onset prostate cancer. Cell BiochemFunct 26:771-7.
[2]     Beatty S, Koh H, Phil M, Henson D, Boulton M. 2000.The role of oxidative stress in the pathogenesis of age-related macular degeneration. Surv Ophthalmol 45: 115-34.
[3]     Boker T, Fang T, Steinmetz R. 1993. Refractive error and choroidal perfusion characteristics in patients with choroidal neovascularization and age-related macular degeneration.Ger J Ophthalmol 2:10-3.
[4]     Capurso C, Solfrizzi V, D’Introno A , Colacicco A , Capurso S, et al. 2008. Short arm of chromosome 11 and sporadic Alzheimer’s disease:CAT and cathepsin D gene polymorphisms. Neuroscience Letters. 432:237–242.
[5]     Cebrian A, Pharoah PD, Ahmed S, Smith PL, Luccarini C, et al. 2006. Tagging Single-Nucleotide Polymorphisms in Antioxidant Defense Enzymes and Susceptibility to Breast Cancer. Cancer Res 66:1225-33.
[6]     Chandrasena LG, Chackrewarthy S, Perera PT, de Silva D. 2006. Erythrocyte antioxidant enzymes in patients with cataract. Ann Clin Lab Sci 36: 201-4.
[7]     Chistiakov DA, Savost’anov KV, Turakulov RI, Titovich EV, Zilberman LI, et al. 2004.A new type 1 diabetes susceptibility locus containing the CAT gene (chromosome 11p13) in a Russian population. Diabetes Metab Res Rev 20: 219-24.
[8]     Clemons TE, Milton RC, Klein R, Seddon JM, Ferris FL. 2005. Risk factors for the incidence of advanced age-related macular degeneration in the age-related eye disease study. Ophthalmology 112:533-9.
[9]     Coleman HR, Chan CC, Ferris FL III, Chew EY. 2008. Age-related macular degeneration. Lancet, 372:1835-45.
[10] Dufour E, Boulay J, Rincheval V, Sainsard-Chanet A. 2000.A causal link between respiration and senescence in Podosporaanserina. Proc Natl Acad Sci USA 97:4138-43.
[11] El Matri L, Bouraoui R, Chebil A, Kort F, Limaiem R, Bouladi M, et al. Prevalence and risk factors of age-related macular degeneration (AMD) in a Tunisian hospital population. Bull SocBelgeOphtalmol 2012; 319:35-41.
[12] Fan AZ, Yesupriya A, Chang Mh, House M, Fang J, et al. 2010. Gene polymorphisms in association with emerging cardiovascular risk markers in adult women. BMC Med Genet 11:6.
[13] Forsberg L, de Faire U, Morgenstern R. 2001(b). Oxidative stress, human genetic variation, and disease. Arch. Biochem. Biophys 389:84-93.
[14] Forsberg L, Lyrenäs L, Faire UD, Morgenstern R. 2001(a). A common functional C-T substitution polymorphism in the promoter region of the human catalase gene influences transcription factor binding, reporter gene transcription and is correlated to blood catalase levels. Free Rad Biol Med 30:500-5.
[15] Funke S, Hoffmeister M, Brenner H, Chang-Claude J. 2009. Effect modification by smoking on the association between genetic polymorphisms in oxidative stress genes and colorectal cancer risk. Cancer Epidemiology Biomarkers & Prevention 18:2336-8.
[16] Gao H, Hollyfield JG. 1992. Aging of the human retina. Differential loss of neurons and retinal pigment epithelial cells. Invest Ophthalmol Vis Sci 33:1-17.
[17] Gehrs KM, Anderson DH, Johnson LV, Hageman GS. 2006. Age-related macular degeneration-emerging pathogenetic and therapeutic concepts. Ann.Med 38:450-71.
[18] Halliwell B, Gutteridge J. M .C. 1989. Free radicals in biology and medicine. Oxford: Clarendon Press, 12:93-5.
[19] He C, Qureshi AA, Han J. 2010. Polymorphisms in genes involved in oxidative stress and their interactions with life style factors on skin cancer risk. Journal of Dermatology science 60:54-6.
[20] Hong Chen, Ming Yu, Ming Li, RuieZha, Qihan Zhu, et al. 2011. Polymorphic variations in manganese superoxide dismutase (MnSOD), glutathione peroxidase-1 (GPX1), and catalase (CAT) contribute to elevated plasma triglyceride levels in Chinese patients with type 2 diabetes or diabetic cardiovascular disease. Molecular Cell Biochemistry 22:610-14.
[21] Hughes AE, Orr N, Esfandiary H, Diaz-Torres M, Goodship T, Chakravarthy U. 2006. A common CFH haplotype, with deletion of CFHR1 and CFHR3, is associated with lower risk of age-related macular degeneration. Nat Genet 38:1173-7.
[22] Islam T, McConnell R, GaudermanW.j, Avo Ed M, Peters J D, Gilliland F. 2007. Ozone, Oxidant Defense Genes, and Risk of Asthma during Adolescence. Am J RespirCrit Care Med 177:388-95.
[23] McCord J M, Fridovich I. 1969. Superoxide dismutase. An enzymic function for erythrocuprein (hemocuprein). J. Biol. Chem 244:6049-55.
[24] Muller FL, Lustgarten MS, Jang Y, Richardson A, Van Remmen H. 2007.Trends in oxidative aging theories. Free Rad Biol Med 43:477-503.
[25] Newton CR. 1995. Mutational analysis: known mutations. In: McPherson MJ, Hames D, Taylor GR (eds) PCR2: a practical approach. IRL-Press, Oxford, p. 219-22.
[26] Oestergaard MZ, Tyrer J, Cebrian A, Shah M, Dunning AM, et al. 2006. Interactions between genes involved in the antioxidant defence system and breast cancer risk. British Journal Cancer 95:525-31.
[27] Ogata M. 1991. Acatalasemia. Hum. Genet, 86:331-40.
[28] Quan F, Korneluk R, Tropak M, Gravel R. 1989. Isolation and characterization of the human catalse gene. Nucleic Acids Res 14:5321-35.
[29] Rafiee L, Saadat I, Saadat M. 2010. Glutathione S-transferase genetic polymorphisms (GSTM1, GSTT1 and GSTO2) in three Iranian populations. Mol Biol Rep 37:155-8.
[30] Rajaraman P, Hutchinson A, Rothman N, Black PM, Fine HA, et al. 2010. DNA repair gene polymorphisms and risk of adult meningioma, glioma and acoustic neuroma. Neuro Oncology 12:37-48.
[31] Rajić V, Aplenc R, Debeljak M, Prestor VV, Karas-Kuzelicki N, et al. 2009. Influence of the polymorphism in candidate genes on late cardiac damage in patients treated due to acute leukemia in childhood. Leuk Lymphoma 50:1693-8.
[32] Sandberg MA, Tolentino MJ, Miller S, Berson EL, Gaudio AR. 1993. Hyperopia and neovascularization in age-related macular degeneration. Ophthalmology 100:1009-13.
[33] Smith W, Mitchell P. 1998. Family history and age-related maculopathy: the blue mountains eye study. Aust. N.Z.J. Ophthalmol 26:203-6.
[34] Spraul CW, Grossniklaus HE. 1997. Characteristics of Drusen and Bruch’s membrane in postmortem eyes with age-related macular degeneration. Arch Ophthalmol 115:267-73.
[35] Tang H, Dong X, Day RS, Hassan MM, Li D. 2010. Antioxidant genes, diabetes and dietary antioxidants in association with risk of pancreatic cancer. Carcinogenesis 31:607-13.
[36] Tilak JC, Boloor KK, Sane Ketaki S, GhaskadbiSaroj S, Lele RD. 2004. Free Radicals and Antioxidants in Human Health: Current Status and Future Prospects. J Assoc Physicians India 52: 796.
[37] Zarbock R, Hendig D, Szliska C, Kleesiek K, Götting C. 2007. Pseudoxanthoma Elasticum: genetic variations in antioxidant genes are risk factors for early disease onset. ClinChem 53:1734-40.
[38] Zhang Y, Lan Z, DongL Is, ZhiSheng Li, Lin W, Ping L. 2011. Genetic polymorphisms of superoxide dismutases, catalase, and glutathione peroxidase in age-related cataract.Mol Vis 17.