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Research Article

Association of oxidative stress-related genes with idiopathic recurrent miscarriage

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Pages 534-541 | Received 28 Dec 2013, Accepted 03 Feb 2014, Published online: 05 Mar 2014

References

  • Coulam CB, Clark DA, Beer AE, Kutteh WH, Silver R, Kwak J, Stephenson M. Clinical Guidelines Recommendation Committee for Diagnosis and Treatment of Recurrent Spontaneous Abortion. Current clinical options for diagnosis and treatment of recurrent spontaneous abortion. Am J Reprod Immunol 1997;38:57–74.
  • Practice Committee of the American Society for Reproductive Medicine. Definitions of infertility and recurrent pregnancy loss: a committee opinion. Fertil Steril 2013;99:63.
  • Christiansen OB, Mathiesen O, Lauritsen JG, Grunnet N. Idiopathic recurrent spontaneous abortion. Evidence of a familial predisposition. Acta Obstet Gynecol Scand 1990;69: 597–601.
  • Miskovic S, Culic V, Konjevoda P, Pavelic J. Positive reproductive family history for spontaneous abortion: predictor for recurrent miscarriage in young couples. Eur J Obstet Gynecol Reprod Biol 2012;161:182–186.
  • Rull K, Nagirnaja L, Laan M. Genetics of recurrent miscarriage: challenges, current knowledge, future directions. Front Genet 2012;3:34.
  • Wang L, Wang ZC, Xie C, Liu XF, Yang MS. Genome-wide screening for risk loci of idiophatic recurrent miscarriage in a Han Chinese population: a pilot study. Reprod Sci 2010;17: 578–584.
  • Kolte AM, Nielsen HS, Moltke I, Degn B, Pedersen B, Sunde L, et al. A genome-wide scan in affected sibling pairs with idiopathic recurrent miscarriage suggests genetic linkage. Mol Hum Reprod 2011;17:379–385.
  • Palm M, Axelsson O, Wernroth L, Basu S. F(2)-isoprostanes, tocopherols and normal pregnancy. Free Radic Res 2009;43: 546–552.
  • Burton GJ, Jauniaux E. Oxidative stress. Best Pract Res Clin Obstet Gynaecol 2011;25:287–299.
  • Agarwal A, Aponte-Mellado A, Premkumar BJ, Shaman A, Gupta S. The effects of oxidative stress on female reproduction: a review. Reprod Biol Endocrinol 2012;10:49.
  • Lyu SW, Song H, Yoon JA, Chin MU, Sung SR, Kim YS, et al. Transcriptional profiling with a pathway-oriented analysis in the placental villi of unexplained miscarriage. Placenta 2013;34:133–140.
  • Hamajima N. PCR–CTPP: a new genotyping technique in the era of genetic epidemiology. Expert Rev Mol Diagn 2001;1:119–123.
  • Sole X, Guino E, Valls J, Iniesta R, Moreno V. SNPStats: a web tool for the analysis of association studies. Bioinformatics 2006;22:1928–1929.
  • Abramson JH. WINPEPI updated: computer programs for epidemiologists, and their teaching potential. Epidemiol Perspect Innov 2011;8:1.
  • Ritchie MD, Hahn LW, Roodi N, Bailey LR, Dupont WD, Parl FF, Moore JH. Multifactor-dimensionality reduction reveals high-order interactions among estro-gen-metabolism genes in sporadic breast cancer. Am J Hum Genet 2001;69:138–147.
  • Zuberi K, Franz M, Rodriguez H, Montojo J, Lopes CT, Bader GD, Morris Q. GeneMANIA prediction server 2013 update. Nucleic Acids Res 2013;41:W115–122.
  • Callaghan R, Crowley E, Potter S, Kerr ID. P-glycoprotein: so many ways to turn it on. J Clin Pharmacol 2008;48:365–378.
  • Masuda M, Nakai E, Mizutani T. Study of oxidized lipids as endogenous substrates of P-gp (ABCB1). Drug Metab Lett 2008;2:238–244.
  • Thévenod F, Friedmann JM, Katsen AD, Hauser IA. Up-regulation of multidrug resistance P-glycoprotein via nuclear factor-kappaB activation protects kidney proximal tubule cells from cadmium- and reactive oxygen species-induced apoptosis. J Biol Chem 2000;275:1887–1896.
  • Kimchi-Sarfaty C, Oh JM, Kim IW, Sauna ZE, Calcagno AM, Ambudkar SV, Gottesman MM. A “silent” polymorphism in the MDR1 gene changes substrate specificity. Science 2007;315:525–528.
  • Hoffmeyer S, Burk O, Von Richter O, Arnold HP, Brockmoller J, Johne A, et al. Functional polymorphisms of the human multidrug-resistance gene: multiple sequence variations and correlation of one allele with P glycoprotein expression and activity in vivo. Proc Natl Acad Sci U S A 2000;97:3473–3478.
  • Yoo HD, Lee YB. Interplay of pharmacogenetic variations in ABCB1 transporters and cytochrome P450 enzymes. Arch Pharm Res 2011;34:1817–1828.
  • Kanasaki K, Palmsten K, Sugimoto H, Ahmad S, Hamano Y, Xie L, et al. Deficiency in catechol-O-methyltransferase and 2-methoxyoestradiol is associated with pre-eclampsia. Nature 2008;453:1117–1121.
  • Thambiraj DF, Rueda-Clausen CF, Stanley J, Poudel R, Davidge S, Baker P. Effects of maternal hypoxia on placental levels of oxidative stress markers in COMT-/- and C57 mice. BMC Proc 2012;6:P10.
  • Lotta T, Vidgren J, Tilgmann C, Ulmanen I, Melen K, Julkunen I, Taskinen J. Kinetics of human soluble and membrane-bound catechol O-methyltransferase: a revised mechanism and description of the thermolabile variant of the enzyme. Biochemistry 1995;34:4202–4210.
  • Gothelf D, Law AJ, Frisch A, Chen J, Zarchi O, Michaelovsky E, et al. Biological effects of COMT haplotypes and psychosis risk in 22q11.2 deletion syndrome. Biol Psychiatry 2014;75:406–413.
  • Roten LT, Fenstad MH, Forsmo S, Johnson MP, Moses EK, Austgulen R, Skorpen F. A low COMT activity haplotype is associated with recurrent preeclampsia in a Norwegian population cohort (HUNT2). Mol Hum Reprod 2011;17:439–446.
  • Lim JH, Kim SY, Kim do J, Park SY, Han HW, Han JY, et al. Genetic polymorphism of catechol-O-methyltransferase and cytochrome P450c17α in preeclampsia. Pharmacogenet Genomics 2010;20:605–610.
  • Liang S, Liu X, Fan P, Liu R, Zhang J, He G, et al. Association between Val158Met functional polymorphism in the COMT gene and risk of preeclampsia in a Chinese population. Arch Med Res 2012;43:154–158.
  • Hill LD, York TP, Kusanovic JP, Gomez R, Eaves LJ, Romero R, Strauss JF III. Epistasis between COMT and MTHFR in maternal-fetal dyads increases risk for preeclampsia. PLoS One 2011;6:e16681.
  • Pérez-Sepúlveda A, Torres MJ, Valenzuela FJ, Larraín R, Figueroa-Diesel H, Galaz J, et al. Low 2-methoxyestradiol levels at the first trimester of pregnancy are associated with the development of pre-eclampsia. Prenat Diagn 2012;32:1053–1058.
  • Brigelius-Flohé R, Maiorino M. Glutathione peroxidases. Biochim Biophys Acta 2013;1830:3289–3303.
  • Ufer C, Wang CC. The roles of glutathione peroxidases during embryo development. Front Mol Neurosci 2011;4:12.
  • Méplan C, Crosley LK, Nicol F, Horgan GW, Mathers JC, Arthur JR, Hesketh JE. Functional effects of a common single-nucleotide polymorphism (GPX4c718t) in the glutathione peroxidase 4 gene: interaction with sex. Am J Clin Nutr 2008; 87:1019–1027.
  • Bermano G, Pagmantidis V, Holloway N, Kadri S, Mowat NA, Shiel RS, et al. Evidence that a polymorphism within the 3’UTR of glutathione peroxidase 4 is functional and is associated with susceptibility to colorectal cancer. Genes Nutr 2007;2: 225–232.
  • Stein TP, Scholl TO, Schluter MD, Leskiw MJ, Chen X, Spur BW, Rodriguez A. Oxidative stress early in pregnancy and pregnancy outcome. Free Radic Res 2008;42: 841–848.
  • Nishizawa H, Suzuki M, Pryor-Koishi K, Sekiya T, Tada S, Kurahashi H, Udagawa Y. Impact of indoleamine 2,3-dioxygenase on the antioxidant system in the placentas of severely pre-eclamptic patients. Syst Biol Reprod Med 2011;57: 174–178.
  • Kimura C, Watanabe K, Iwasaki A, Mori T, Matsushita H, Shinohara K, Wakatsuki A. The severity of hypoxic changes and oxidative DNA damage in the placenta of early-onset preeclamptic women and fetal growth restriction. J Matern Fetal Neonatal Med 2013;26:491–496.
  • Hsieh TT, Chen SF, Lo LM, Li MJ, Yeh YL, Hung TH. The association between maternal oxidative stress at mid-gestation and subsequent pregnancy complications. Reprod Sci. 2012; 19:505–512.
  • Negi R, Pande D, Kumar A, Khanna RS, Khanna HD. In vivo oxidative DNA damage and lipid peroxidation as a biomarker of oxidative stress in preterm low-birthweight infants. J Trop Pediatr 2012;58:326–328.
  • Wells PG, Bhuller Y, Chen CS, Jeng W, Kasapinovic S, Kennedy JC, et al. Molecular and biochemical mechanisms in teratogenesis involving reactive oxygen species. Toxicol Appl Pharmacol 2005;207:354–366.
  • Lee AJ, Hodges NJ, Chipman JK. Interindividual variability in response to sodium dichromate-induced oxidative DNA damage: role of the Ser326Cys polymorphism in the DNA-repair protein of 8-oxo-7,8-dihydro-2’-deoxyguanosine DNA glycosylase 1. Cancer Epidemiol Biomarkers Prev 2005;14:497–505.
  • Bravard A, Vacher M, Moritz E, Vaslin L, Hall J, Epe B, Radicella JP. Oxidation status of human OGG1-S326C polymorphic variant determines cellular DNA repair capacity. Cancer Res 2009;69:3642–3649.
  • Jauniaux E, Watson AL, Hempstock J, Bao YP, Skepper JN, Burton GJ. Onset of maternal arterial blood flow and placental oxidative stress. A possible factor in human early pregnancy failure. Am J Pathol 2000;157:2111–2122.
  • Uzun A, Dewan AT, Istrail S, Padbury JF. Pathway-based genetic analysis of preterm birth. Genomics 2013;101:163–170.
  • Stuart JM, Segal E, Koller D, Kim SK. A gene-coexpression network for global discovery of conserved genetic modules. Science 2003;302:249–255.
  • Simonelli V, Mazzei F, D’Errico M, Dogliotti E. Gene susceptibility to oxidative damage: from single nucleotide polymorphisms to function. Mutat Res 2012;731:1–13.

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