The relationship of retinopathy of prematurity with brain-derivated neurotrophic factor, vascular endotelial growth factor-A, endothelial PAD domain protein 1 and nitric oxide synthase 3 gene polymorphisms

References

• Section on Ophthalmology American Academy of Pediatrics; American Academy of Ophthalmology; American Association for Pediatric Ophthalmology and Strabismus. Screening examination of premature infants for retinopathy of prematurity. Pediatrics. 2006 Feb;117(2):572–6. doi:https://doi.org/10.1542/peds.2005-2749. Erratum in: Pediatrics. 2006 Sep;118(3):1324. PMID: 16452383
   Google Scholar
• Başmak H, Niyaz L, Sahin A, Erol N, Gürsoy HH. Retinopathy of prematurity: screening guidelines need to be reevaluated for developing countries. Eur J Ophthalmol. 2010 Jul-Aug;20(4):752–55. eng. Epub 2010/ 02/16. doi:https://doi.org/10.1177/112067211002000417. Cited in: Pubmed; PMID 20155710.
   PubMed Web of Science ®Google Scholar
• Chan-Ling T, Gole GA, Quinn GE, Adamson SJ, Darlow B, Research E. Pathophysiology, screening and treatment of ROP: a multi-disciplinary perspective. Prog Retin Eye Res. 2018;62:77–119.
   Google Scholar
• MacDonald M, Goldberg Y, Macfarlane J, Samuels M, Trese M, Shastry B. Genetic variants of frizzled‐4 gene in familial exudative vitreoretinopathy and advanced retinopathy of prematurity. Clin Genet. 2005;67(4):363–66.
   Google Scholar
• Hutcheson KA, Paluru PC, Bernstein SL, Koh J, Rappaport EF, Leach RA, Young TL. Norrie disease gene sequence variants in an ethnically diverse population with retinopathy of prematurity. Mol Vis. 2005;11:501–08.
   Google Scholar
• Poggi C, Giusti B, Gozzini E, Sereni A, Romagnuolo I, Kura A, Pasquini E, Abbate R, Dani C. Genetic contributions to the development of complications in preterm newborns. PLoS One. 2015;10(7):e0131741.
   Google Scholar
• Hartnett ME, Morrison MA, Smith S, Yanovitch TL, Young TL, Colaizy T, Momany A, Dagle J, Carlo WA, Clark EA, et al. Genetic variants associated with severe retinopathy of prematurity in extremely low birth weight infants. Invest Ophthalmol Vis Sci. 2014;55(10):6194–203.
   Google Scholar
• Mohamed S, Schaa K, Cooper ME, Ahrens E, Alvarado A, Colaizy T, Marazita ML, Murray JC, Dagle JM. Genetic contributions to the development of retinopathy of prematurity. Pediatr Res. 2009;65(2):193–97.
   Google Scholar
• Aydin H, Gunay M, Celik G, Gunay BO, Aydin UT, Karaman A. Evaluation of factor V Leiden, Prothrombin G20210A, MTHFR C677T and MTHFR A1298C gene polymorphisms in retinopathy of prematurity in a Turkish cohort. Ophthalmic Genet. 2016 Dec;37(4):415–18. Epub 2016/ 11/03. doi:https://doi.org/10.3109/13816810.2015.1126611. Cited in: Pubmed; PMID 27018927.
   PubMed Web of Science ®Google Scholar
• Revised indications for the treatment of retinopathy of prematurity: results of the early treatment for retinopathy of prematurity randomized trial. Arch Ophthalmol. 2003 Dec;121(12):1684–94. eng. Epub 2003/ 12/10. doi:https://doi.org/10.1001/archopht.121.12.1684. Cited in: Pubmed; PMID 14662586.
   PubMed Web of Science ®Google Scholar
• Early Treatment For Retinopathy Of Prematurity Cooperative Group. Revised indications for the treatment of retinopathy of prematurity: results of the early treatment for retinopathy of prematurity randomized trial. Arch Ophthalmol. 2003. Dec;121(12):1684–94. doi:https://doi.org/10.1001/archopht.121.12.1684. PMID: 14662586
   Google Scholar
• Kalmeh ZA, Azarpira N, Mosallaei M, Hosseini H, Malekpour Z. Genetic polymorphisms of vascular endothelial growth factor and risk for retinopathy of prematurity in South of Iran. Mol Biol Rep. 2013;40(7):4613–18.
   Google Scholar
• Ali AA, Hussien NF, Samy RM. Husseiny KA. Polymorphisms of vascular endothelial growth factor and retinopathy of prematurity. J Pediatr Ophthalmol Strabismus. 2015;52(4):245–53.
   Google Scholar
• Hartnett M, Morrison M, Page G, Cotten M, Murray J, DeAngelis M.Candidate gene study of retinopathy of prematurity in extremely low birthweight infants from the neonatal research network. Steroids. 2013;218(82.9):82.9.
   Google Scholar
• Yagi M, Yamamori M, Morioka I, Yokoyama N, Honda NA. VEGF 936C> T is predictive of threshold retinopathy of prematurity in Japanese infants with a 30-week gestational age or less. Res Rep Neonatol. 2011;1:5–11.
   Google Scholar
• Fiorentino F, Magli MC, Podini D, Ferraretti AP, Nuccitelli A, Vitale N, Baldi M, Gianaroli L. The minisequencing method: an alternative strategy for preimplantation genetic diagnosis of single gene disorders. Mol Hum Reprod. 2003 Jul 9;(7):399–410. Epub 2003/ 06/13. doi:https://doi.org/10.1093/molehr/gag046. Cited in: Pubmed; PMID 12802047.
   Google Scholar
• Turner S, Armstrong LL, Bradford Y, Carlson CS, Crawford DC, Crenshaw AT, de Andrade M, Doheny KF, Haines JL, Hayes G, et al. Quality control procedures for genome-wide association studies. Curr Protoc Hum Genet. 2011 Jan;68(1). Chapter 1: Unit119. Epub 2011/ 01/15. doi:https://doi.org/10.1002/0471142905.hg0119s68. Cited in: Pubmed; PMID 21234875.
   Google Scholar
• Salanti G, Amountza G, Ntzani EE, Ioannidis JP. Hardy-Weinberg equilibrium in genetic association studies: an empirical evaluation of reporting, deviations, and power. Eur J Hum Genet. 2005 Jul;13(7):840–48. Epub 2005/ 04/14. doi:https://doi.org/10.1038/sj.ejhg.5201410. Cited in: Pubmed; PMID 15827565.
   PubMed Web of Science ®Google Scholar
• Cooke RWI, Drury JA, Mountford R, Clark D. Genetic polymorphisms and retinopathy of prematurity. Invest Ophthalmol Vis Sci. 2004;45(6):1712–15. doi:https://doi.org/10.1167/iovs.03-1303.
   PubMed Web of Science ®Google Scholar
• Yu C, Yi J, Yin X, Deng Y, Liao Y, Li X.Correlation of interactions between NOS3 polymorphisms and oxygen therapy with retinopathy of prematurity susceptibility. Int J Clin Exp Pathol. 2015;8(11):15250–15254. eng.
   PubMed Web of Science ®Google Scholar
• Chen J, Smith LE. Retinopathy of prematurity. Angiogenesis. 2007;10(2):133–40. Epub 2007/ 03/03. doi:https://doi.org/10.1007/s10456-007-9066-0. Cited in: Pubmed; PMID 17332988.
   PubMedGoogle Scholar
• Kaya M, Cokakli M, Berk AT, Yaman A, Yesilirmak D, Kumral A, Atabey N. Associations of VEGF/VEGF-receptor and HGF/c-Met promoter polymorphisms with progression/regression of retinopathy of prematurity. Curr Eye Res. 2013 Jan;38(1):137–42. Epub 2012/ 10/26. doi:https://doi.org/10.3109/02713683.2012.731550. Cited in: Pubmed; PMID 23094709.
   PubMed Web of Science ®Google Scholar
• Vannay A, Dunai G, Banyasz I, Szabo M, Vamos R, Treszl A, Hajdu J, Tulassay T, Vasarhelyi B. Association of genetic polymorphisms of vascular endothelial growth factor and risk for proliferative retinopathy of prematurity. Pediatr Res. 2005 Mar;57(3):396–98. eng. Epub 2005/ 01/07. doi:https://doi.org/10.1203/01.Pdr.0000153867.80238.E0. Cited in: Pubmed; PMID 15635051.
   PubMed Web of Science ®Google Scholar
• Ghadyani M, Noorishadkam M, Hosseini-Jangjou SH, Bahrami R, Akbarian E, Saeida-Ardekani M, Neamatzadeh H, Zare Z. Association of-634 C/G polymorphism at vascular endothelial growth factor gene with risk retinopathy of prematurity. World J Peri & Neonatol. 2020. doi:https://doi.org/10.18502/wjpn.v3i1.5060.
   Google Scholar
• Ciais D, Cherradi N, Bailly S, Grenier E, Berra E, Pouyssegur J, LaMarre J, Feige -J-J. Destabilization of vascular endothelial growth factor mRNA by the zinc-finger protein TIS11b. Oncogene. 2004;23(53):8673–80. doi:https://doi.org/10.1038/sj.onc.1207939.
   PubMed Web of Science ®Google Scholar
• Pagès G, Pouysségur J. Transcriptional regulation of the Vascular Endothelial Growth Factor gene–a concert of activating factors. Cardiovasc Res. 2005;65(3):564–73. doi:https://doi.org/10.1016/j.cardiores.2004.09.032.
   PubMed Web of Science ®Google Scholar
• Ray PS, Jia J, Yao P, Majumder M, Hatzoglou M, Fox PL. A stress-responsive RNA switch regulates VEGFA expression. Nature. 2009;457(7231):915–19.
   Google Scholar
• Krippl P, Langsenlehner U, Renner W, Yazdani‐Biuki B, Wolf G, Wascher TC, Paulweber B, Haas J, Samonigg H. A common 936 C/T gene polymorphism of vascular endothelial growth factor is associated with decreased breast cancer risk. Int J Cancer. 2003;106(4):468–71. doi:https://doi.org/10.1002/ijc.11238.
   PubMed Web of Science ®Google Scholar
• Zhai R, Gong MN, Zhou W, Thompson TB, Kraft P, Su L, Christiani DC. Genotypes and haplotypes of the VEGF gene are associated with higher mortality and lower VEGF plasma levels in patients with ARDS. Thorax. 2007;62(8):718–22. doi:https://doi.org/10.1136/thx.2006.069393.
   PubMed Web of Science ®Google Scholar
• Renner W, Kotschan S, Hoffmann C, Obermayer-Pietsch B, Pilger E. A common 936 C/T mutation in the gene for vascular endothelial growth factor is associated with vascular endothelial growth factor plasma levels. J Vas Res. 2000;37(6):443–48. doi:https://doi.org/10.1159/000054076.
   PubMed Web of Science ®Google Scholar
• Langmia IM, Apalasamy YD, Omar SZ, Mohamed Z. Association of VEGFA gene polymorphisms and VEGFA plasma levels with spontaneous preterm birth. Pharmacogenet Genom. 2015 Apr;25(4):199–204. Epub 2015/ 02/26. doi:https://doi.org/10.1097/FPC.0000000000000125. Cited in: Pubmed; PMID 25714003.
   PubMed Web of Science ®Google Scholar
• Tian-wen Z, Yong-hong Z, Yan C.Meta analysis of relationship between polymorphism of genes of vascular endothelial growth factor and advanced retinopathy of prematurity. J Shanghai Jiaotong Univ. 2014;34(5):681.
   Google Scholar
• Shastry BS, Qu X. Lack of association of the VEGF gene promoter (−634 G–>C and −460 C–>T) polymorphism and the risk of advanced retinopathy of prematurity. Graefes Arch Clin Exp Ophthalmol. 2007 May;245(5):741–43. Epub 2006/ 11/23. doi:https://doi.org/10.1007/s00417-006-0480-6. Cited in: Pubmed; PMID 17119993.
   PubMed Web of Science ®Google Scholar
• Shukla S, Malik MA, Chandra P, Kaur J. Association between VEGF polymorphisms (−460 T/C and +936 C/T) and retinopathy of prematurity risk: a meta-analysis. Saudi J Ophthalmol. 2016 Jul-Sep;30(3):157–62. Epub 2017/ 02/18. doi:https://doi.org/10.1016/j.sjopt.2016.06.003. Cited in: Pubmed; PMID 28210175.
   PubMed Web of Science ®Google Scholar
• Grishanin RN, Yang H, Liu X, Donohue-Rolfe K, Nune GC, Zang K, Xu B, Duncan JL, Lavail MM, Copenhagen DR, et al. Retinal TrkB receptors regulate neural development in the inner, but not outer, retina. Mol Cell Neurosci. 2008 Jul;38(3):431–43. Epub 2008/ 05/31. doi:https://doi.org/10.1016/j.mcn.2008.04.004. Cited in: Pubmed; PMID 18511296.
   PubMed Web of Science ®Google Scholar
• Rao S, Chun C, Fan J, Kofron JM, Yang MB, Hegde RS, Ferrara N, Copenhagen DR, Lang RA. A direct and melanopsin-dependent fetal light response regulates mouse eye development. Nature. 2013 Feb 14;494(7436):243–46. Epub 2013/ 01/22. doi:https://doi.org/10.1038/nature11823. Cited in: Pubmed; PMID 23334418.
   PubMed Web of Science ®Google Scholar
• Morita M, Ohneda O, Yamashita T, Takahashi S, Suzuki N, Nakajima O, Kawauchi S, Ema M, Shibahara S, Udono T, et al. HLF/HIF-2alpha is a key factor in retinopathy of prematurity in association with erythropoietin. EMBO J. 2003 Mar 3;22(5):1134–46. Epub 2003/ 02/28. doi:https://doi.org/10.1093/emboj/cdg117. Cited in: Pubmed; PMID 12606578.
   PubMed Web of Science ®Google Scholar
• Rusai K, Vannay A, Szebeni B, Borgulya G, Fekete A, Vásárhelyi B, Tulassay T, Szabó AJ. Endothelial nitric oxide synthase gene T-786C and 27-bp repeat gene polymorphisms in retinopathy of prematurity. Mol Vis. 2008 Feb 5;14:286–90. eng. Epub 2008/ 03/13. Cited in: Pubmed; PMID 18334945.
   PubMed Web of Science ®Google Scholar
• Gohari M, Dastgheib SA, Noorishadkam M, Lookzadeh MH, Mirjalili SR, Akbarian-Bafghi MJ, Morovati-Sharifabad M, Neamatzadeh H. Association of eNOS and ACE polymorphisms with retinopathy of prematurity: a systematic review and meta-analysis. Fetal Pediatr Pathol. 2020 Aug;39(4):334–345.
   Web of Science ®Google Scholar