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Research Article

Genetic polymorphisms of antioxidant enzymes as risk factors for oxidative stress-associated complications in preterm infants

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Pages 1130-1139 | Received 02 Apr 2012, Accepted 08 May 2012, Published online: 13 Jun 2012

References

  • Maltepe E, Saugstad OD. Oxygen in health and disease: regulation of oxygen homeostasis—clinical implications. Pediatr Res 2009;65:261–268.
  • Perrone S, Tataranno ML, Negro S, Longini M, Marzocchi B, Proietti F, . Early identification of the risk for free radical-related diseases in preterm newborns. Early Hum Dev 2010; 86:241–244.
  • Buhimschi IA, Buhimschi CS, Pupkin M, Weiner CP. Beneficial impact of term labor: nonenzymatic antioxidant reserve in the human fetus. Am J Obstet Gynecol 2003;189; 181–188.
  • Rubaltelli FF, Dani C, Reali MF, Bertini G, Wiechmann L, Tangucci M, Spagnolo A, the Italian Group of Neonatal Pneumology. Acute neonatal respiratory distress in Italy: a one year prospective study. Acta Paediatr 1988;87: 1261–1268.
  • Gitto E, Reiter RJ, Karbownik M, Xian-Tan D, Barberi I. Respiratory distress syndrome in the newborn: role of oxidative stress. Intensive Care Med 2001;27:1116–1123.
  • Pierce M, Bancalari E. The role of inflammation in the pathogenesis of bronchopulmonary dysplasia. Pediatr Pulmonol 1995;19:371–378.
  • Worthen GS, Haslett C, Rees AJ, Gumbay RS, Henson JE, Henson PM. Neutrophil-mediated pulmonary vascular injury. Am Rev Resp Dis 1987;136:19–28.
  • Davis JM, Rosenfeld W. Chronic lung disease. In: Avery GB, Fletcher MA, MacDonald MD, (eds). Neonatology, 5th ed. Philadelphia, PA: Lippincott; 1999. pp. 509–532.
  • Saugstad OD. Bronchopulmonary dysplasia-oxidative stress and antioxidants. Seminar Neonatol 2003;8:39–49.
  • Bassan H. Intracranial hemorrhage in the preterm infant: understanding it, preventing it. Clin Perinatol 2009;36: 737–762.
  • Drack AV. Preventing blindness in premature infants. N Engl J Med 1998;338:1620–1621.
  • Hardy RJ, Good WV, Dobson V, Palmer EA, Phelps DL, Quintos M, Tung B; Early Treatment for Retinopathy of Prematurity Cooperative Group. Multicenter trial of early treatment for retinopathy of prematurity: study design. Control Clin Trials 2004;25:311–325.
  • Good WV, Hardy RJ, Dobson V, Palmer EA, Phelps DL, Quintos M, Tung B; Early Treatment for Retinopathy of Prematurity Cooperative Group. The incidence and course of retinopathy of prematurity: findings from the early treatment for retinopathy of prematurity study. Pediatrics 2005;116: 15–23.
  • Dani C, Martelli E, Bertini G, Pezzati M, Rossetti M, Buonocore G, . Effect of blood transfusions on oxidative stress in preterm infants. Arch Dis Child Fetal Neonatal Ed 2004;89:F408–F411.
  • Dani C, Corsini I, Bertini G, Pratesi S, Barp J, Rubaltelli FF. Effect of multiple INSURE procedures in extremely preterm infants. J Matern Fetal Neonatal Med 2011;24: 1427–1431.
  • Miao L, St Clair DK. Regulation of superoxide dismutase genes: implications in disease. Free Radic Biol Med 2009; 47:344–356.
  • American Academy of Pediatric's Committee on drugs, Committee on fetus and newborn and Committee on Infectious Diseases. Pediatrics 1980;65:1047–1053.
  • Ehrenkranz RA, Walsh MC, Vohr BR, Jobe AH, Wright LL, Fanaroff AA, ; National Institutes of Child Health and Human Development Neonatal Research Network. Validation of the National Institutes of Health consensus definition of bronchopulmonary dysplasia. Pediatrics 2005;116: 1353–1360.
  • Papile LS, Burstein J, Burstein R, Keffler H. Incidence and evolution of the sub-ependymal intraventricular hemorrhage; a study of infants weighing less than 1500 grams. J Pediatr 1978;92:529–534.
  • de Vries LS, Eken P, Dubowitz LM. The spectrum of leukomalacia using cranial ultrasounds. Behav Brain Res 1992; 49:1–6.
  • Bell MJ, Ternberg JL, Feigin RD, Keating JP, Marshall R, Barton L, Brotherton T. Neonatal necrotizing enterocolitis: Therapeutic decisions based upon clinical staging. Ann Surg 1978;187:1–12.
  • Al-Kateb H, Boright AP, Mirea L, Xie X, Sutradhar R, Mowjoodi A, ; Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications Research Group. Multiple superoxide dismutase 1/ splicing factor serine alanine 15 variants are associated with the development and progression of diabetic nephropathy: the Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications Genetics study. Diabetes 2008;57:218–228.
  • Hiroi S, Harada H, Nishi H, Satoh M, Nagai R, Kimura A. Polymorphisms in the SOD2 and HLA-DRB1 genes are associated with nonfamilial idiopathic dilated cardiomyopathy in Japanese. Biochem Biophys Res Commun 1999;261:332–339.
  • Kakko S, Päivänsalo M, Koistinen P, Kesäniemi YA, Kinnula VL, Savolainen MJ. The signal sequence polymorphism of the MnSOD gene is associated with the degree of carotid atherosclerosis. Atherosclerosis 2003;168:147–152.
  • Ambrosone CB, Coles BF, Freudenheim JL, Shields PG. Glutathione-S-transferase (GSTM1) genetic polymorphisms do not affect human breast cancer risk, regardless of dietary antioxidants. J Nutr 1999;129(2S Suppl):565S–568S.
  • Woodson K, Tangrea JA, Lehman TA, Modali R, Taylor KM, Snyder K, . Manganese superoxide dismutase (MnSOD) polymorphism, alpha-tocopherol supplementation and prostate cancer risk in the alpha-tocopherol, beta-carotene cancer prevention study (Finland). Cancer Causes Control 2003;14: 513–518.
  • Stoehlmacher J, Ingles SA, Park DJ, Zhang W, Lenz HJ. The -9Ala/-9Val polymorphism in the mitochondrial targeting sequence of the manganese superoxide dismutase gene (MnSOD) is associated with age among Hispanics with colorectal carcinoma. Oncol Rep 2002;9:235–238.
  • Hsueh YM, Lin P, Chen HW, Shiue HS, Chung CJ, Tsai CT, . Genetic polymorphisms of oxidative and antioxidant enzymes and arsenic-related hypertension. J Toxicol Environ Health A 2005;68:1471–1484.
  • Van Landeghem GF, Tabatabaie P, Beckman G, Beckman L, Andersen PM. Manganese-containing superoxide dismutase signal sequence polymorphism associated with sporadic motor neuron disease. Eur J Neurol 1999;6:639–644.
  • Shimoda-Matsubayashi S, Matsumine H, Kobayashi T, Nakagawa-Hattori Y, Shimizu Y, Mizuno Y. Structural dimorphism in the mitochondrial targeting sequence in the human manganese superoxide dismutase gene. A predictive evidence for conformational change to influence mitochondrial transport and a study of allelic association in Parkinson's disease. Biochem Biophys Res Commun 1996;226:561–565.
  • Wiener HW, Perry RT, Chen Z, Harrell LE, Go RC. A polymorphism in SOD2 is associated with development of Alzheimer's disease. Genes Brain Behav 2007;6:770–775.
  • Tamai M, Furuta H, Kawashima H, Doi A, Hamanishi T, Shimomura H, . Extracellular superoxide dismutase gene polymorphism is associated with insulin resistance and the susceptibility to type 2 diabetes. Diabetes Res Clin Pract 2006;71:140–145.
  • Ye LX, Yang MP, Qiu H, Guo KQ, Yan JS. Association of the polymorphism in manganese superoxide dismutase gene with diabetic retinopathy in Chinese type 2 diabetic patients] Zhonghua Yi Xue Yi Chuan Xue Za Zhi 2008;25:452–454.
  • Petrovic MG, Cilensek I, Petrovic D. Manganese superoxide dismutase gene polymorphism (V16A) is associated with diabetic retinopathy in Slovene (Caucasians) type 2 diabetes patients. Dis Markers 2008;24:59–64.
  • Gotoh N, Yamada R, Matsuda F, Yoshimura N, Iida T. Manganese superoxide dismutase gene (SOD2) polymorphism and exudative age-related macular degeneration in the Japanese population. Am J Ophthalmol 2008;146:146.
  • Soerensen M, Christensen K, Stevnsner T, Christiansen L. The Mn-superoxide dismutase single nucleotide polymorphism rs4880 and the glutathione peroxidase 1 single nucleotide polymorphism rs1050450 are associated with aging and longevity in the oldest old. Mech Ageing Dev 2009;130:308–314.
  • Wan XS, Devalaraja MN, St Clair DK. Molecular structure and organization of the human manganese superoxide dismutase gene. DNA Cell Biol 1994;13:1127–1136.
  • Dahl M, Bowler RP, Juul K, Crapo JD, Levy S, Nordestgaard BG. Superoxide dismutase 3 polymorphism associated with reduced lung function in two large populations. Am J Respir Crit Care Med 2008;178:906–912.
  • Campo S, Sardo AM, Campo GM, D'Ascola A, Avenoso A, Castaldo M, . Extracellular superoxide dismutase (EC-SOD) gene mutations screening in a sample of Mediterranean population. Mutat Res 2005;578: 143–148.
  • Samoila OC, Carter AM, Futers ST, Otiman G, Anghel A, Tamas L, Seclaman E. Polymorphic variants of extracellular superoxide dismutase gene in a Romanian population with atheroma. Biochem Genet 2008;46:634–643.
  • Rosta K, Molvarec A, Enzsöly A, Nagy B, Rónai Z, Fekete A, . Association of extracellular superoxide dismutase (SOD3) Ala40Thr gene polymorphism with pre-eclampsia complicated by severe fetal growth restriction. Eur J Obstet Gynecol Reprod Biol 2009;142:134–138.
  • Marklund SL, Nilsson P, Israelsson K, Schampi I, Peltonen M, Asplund K. Two variants of extracellular superoxide dismutase: relationship to cardiovascular risk factors in an unselected middle-aged population. J Intern Med 1997;242: 5–14.
  • Zelko IN, Mariani TJ, Folz RJ. Superoxide dismutase multigene family: a comparison of the CuZn-SOD (SOD1), Mn-SOD (SOD2), and EC-SOD (SOD3) gene structures, evolution, and expression. Free Radic Biol Med 2002;33: 337–349.
  • Chu Y, Alwahdani A, Iida S, Lund DD, Faraci FM, Heistad DD. Vascular effects of the human extracellular superoxide dismutase R213G variant. Circulation 2005;112: 1047–1053.
  • Forsberg L, Lyrenas L, de Faire U, Morgenstern R. 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 2001;30: 500–505.
  • Kim TH, Hong JM, Oh B, Cho YS, Lee JY, Kim HL, . Genetic association study of polymorphisms in the catalase gene with the risk of osteonecrosis of the femoral head in the Korean population. Osteoarthritis Cartilage 2008;16: 1060–1066.
  • Scheet P, Stephens M. A fast and flexible statistical model for large-scale population genotype data: applications to inferring missing genotypes and haplotypic phase. Am J Hum Genet 2006;78:629–644.
  • Becker T, Cichon S, Jonson E, Knapp M. Multiple testing in the context of haplotype analysis revisited: application to case-control data. Ann Hum Genet 2005;69:747–756.
  • Bastaki M, Huen K, Manzanillo P, Chande N, Chen C, Balmes JR, . Genotype-activity relationship for Mn- superoxide dismutase, glutathione peroxidase 1 and catalase in humans. Pharmacogenet Genomics 2006;16:279–286.
  • Sheng H, Bart RD, Oury TD, Pearlstein RD, Crapo JD, Warner DS. Mice overexpressing extracellular superoxide dismutase have increased resistance to focal cerebral ischemia. Neuroscience 1999;88:185–191.
  • Sheng H, Kudo M, Mackensen GB, Pearlstein RD, Crapo JD, Warner DS. Mice overexpressing extracellular superoxide dismutase have increased resistance to global cerebral ischemia. Exp Neurol 2000;163:392–398.
  • Sheng H, Brady TC, Pearlstein RD, Crapo JD, Warner DS. Extracellular superoxide dismutase deficiency worsens outcome from focal cerebral ischemia in the mouse. Neurosci Lett 1999;267:13–16.
  • Naganuma T, Nakayama T, Sato N, Fu Z, Soma M, Aoi N, . Association of extracellular superoxide dismutase gene with cerebral infarction in women: a haplotype-based case-control study. Hereditas 2008;145:283–292.
  • Sørheim IC, DeMeo DL, Washko G, Litonjua A, Sparrow D, Bowler R, ; International COPD Genetics Network Investigators. Polymorphisms in the superoxide dismutase-3 gene are associated with emphysema in COPD. COPD 2010; 7:262–268.
  • Faraci FM. Protecting against vascular disease in brain. Am J Physiol Heart Circ Physiol 2011;300:H1566–H1582.
  • Ballabh P. Intraventricular hemorrhage in premature infants: mechanism of disease. Pediatr Res 2010;67:1–8.
  • Mak JC, Leung HC, Ho SP, Ko FW, Cheung AH, Ip MS, Chan-Yeung MM. Polymorphisms in manganese superoxide dismutase and catalase genes: functional study in Hong Kong Chinese asthma patients. Clin Exp Allergy 2006;36:440–447.
  • Watanabe Y, Metoki H, Ohkubo T, Katsuya T, Tabara Y, Kikuya M, . Accumulation of common polymorphisms is associated with development of hypertension: a 12-year follow-up from the Ohasama study. Hypertens Res 2010;33: 129–134.
  • Liu YM, Li XD, Guo X, Liu B, Lin AH, Ding YL, Rao SQ. SOD2 V16A SNP in the mitochondrial targeting sequence is associated with noise induced hearing loss in Chinese workers. Dis Markers 2010;28:137–147.

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