Cigarettes contain many toxic and harmful compounds. There are approximately 600 substances in cigarette that produce more than 7,000 chemicals when burned. In general, these compounds are hazardous either for smokers or both smokers and passive smokers. Today, due to the increasing number of female smokers, especially mothers who smoke during pregnancy, fetuses and children are faced with serious and irreparable consequences. Nicotine (the addictive substance in cigarettes), carbon monoxide, and numerous other poisons inhaled from cigarettes are transported through the bloodstream, which can be harmful to health of the fetus and the development of its organs, such as the fetal brain. Smoking has consequences not only during pregnancy but also during breastfeeding. In addition to the aforementioned, smoking is considered as one of the most concerning teratogens which can cause structural or functional abnormality, growth restriction, birth defects, and so on. These consequences can have dramatic and significant effects on infancy, childhood, and adulthood. According to the contents, in this review we try to discuss influences of smoking on the development of the fetus, growth of children, and eventually its effects on the development of congenital disorders.
Erlingsdottir A, Sigurdsson EL, Jonsson JS, Kristjansdottir H, Sigurdsson JA. Smoking during pregnancy: childbirth and health study in primary care in Iceland. Scand J Prim Health Care 2014; 32(1): 11-6.
Mund M, Louwen F, Klingelhoefer D, Gerber A. Smoking and pregnancy--a review on the first major environmental risk factor of the unborn. Int J Environ Res Public Health 2013; 10(12): 6485-99.
Abou El–Ardat M, Izetbegovic S, Abou El-Ardat KA. Effect of Cigarette Smoking in Pregnancy on Infants Anthropometric Characteristics. Mater Sociomed 2014; 26(3): 186-7.
Banderali G, Martelli A, Landi M, Moretti F, Betti F, Radaelli G, et al. Short and long term health effects of parental tobacco smoking during pregnancy and lactation: a descriptive review. J Transl Med 2015; 13: 327.
Suter M, Abramovici A, Showalter L, Hu M, Do Shope C, Varner M, Aagaard-Tillery K, et al. In utero tobacco exposure epigenetically modifies placental CYP1A1 expression. Metabolism 2010; 59(10): 1481-90.
Suter MA, Anders AM, Aagaard KM.. Maternal smoking as a model for environmental epigenetic changes affecting birthweight and fetal programming. Mol Hum Reprod 2013; 19(1): 1-6.
Garrabou G, Hernàndez AS, Garcí MC, Morén C, Tobías E, Córdoba S, et al. Molecular basis of reduced birth weight in smoking pregnant women: mitochondrial dysfunction and apoptosis. Addict Biol 2016; 21(1): 159-70.
Holbrook BD. The effects of nicotine on human fetal development. Birth Defects Res C Embryo Today 2016; 108(2): 181-92.
Marangoni F, Colombo C, de Angelis L, Gambaro V, Agostoni C, Giovannini M, et al. Cigarette smoke negatively and dose-dependently affects the biosynthetic pathway of the n− 3 polyunsaturated fatty acid series in human mammary epithelial cells. Lipids 2004; 39(7): 633-7.
Suter M, Abramovici A, Aagaard-Tillery K. Genetic and epigenetic influences associated with intrauterine growth restriction due to in utero tobacco exposure. Pediatr Endocrinol Rev 2010; 8(2): 94-102.
Polanska, K., et al., Effect of prenatal polycyclic aromatic hydrocarbons exposure on birth outcomes: the Polish mother and child cohort study. Biomed Res Int, 2014. 2014: p. 408939.
Ikeh-Tawari, E.P., J.I. Anetor, and M.A. Charles-Davies, Cadmium level in pregnancy, influence on neonatal birth weight and possible amelioration by some essential trace elements. Toxicol Int, 2013. 20(1): p. 108-12.
Booij L, Benkelfat C, Leyton M, Vitaro F, Gravel P, Lévesque ML, et al. Perinatal effects on in vivo measures of human brain serotonin synthesis in adulthood: a 27-year longitudinal study. European Neuropsychopharmacology 2012; 22(6): 419-23.
Ekblad M, Korkeila J, Lehtonen L. Smoking during pregnancy affects foetal brain development. Acta Paediatr 2015; 104(1): 12-8.
Duncan JR, Byard RW. SIDS Sudden infant and early childhood death: The past, the present and the future. Adelaide, Australia: University of Adelaide Press; 2018. p. 846.
Slotkin T, Lappi SE, McCook EC, Lorber BA, Seidler FJ. Loss of neonatal hypoxia tolerance after prenatal nicotine exposure: implications for sudden infant death syndrome. Brain Res Bull 1995; 38(1): 69-75.
Wickstrom R. Effects of nicotine during pregnancy: human and experimental evidence. Current Neuropharmacol 2007; 5(3): 213-22.
Lavezzi AM, Corna MF, Repetti ML, Matturri L. Cerebellar Purkinje cell vulnerability to prenatal nicotine exposure in sudden unexplained perinatal death. Folia Neuropathol 2013; 51(4): 290-301.
Ding G, Yu J, Chen Y, Vinturache A, Pang Y, Zhang J. Maternal smoking during pregnancy and necrotizing enterocolitis-associated infant mortality in preterm babies. Sci Rep 2017; 7: 45784.
Downard CD, Grant SN, Maki AC, Krupski MC, Matheson PJ, Bendon RW, et al. Maternal cigarette smoking and the development of necrotizing enterocolitis. Pediatrics 2012; 130(1): 78-82.
Ino T. Maternal smoking during pregnancy and offspring obesity: Meta‐analysis. Pediatr Int 2010; 52(1): 94-9.
Oken E, Levitan EB, Gillman MW. Levitan, and M. Gillman, Maternal smoking during pregnancy and child overweight: systematic review and meta-analysis. Int J Obes (Lond). 2008; 32(2): 201-10.
Sunday S, Kabir Z. Impact of carers’ smoking status on childhood obesity in the growing up in Ireland cohort study. Int J Environ Res Public Health 2019; 16(15): 2759.
Wen X, Eiden RD, Justicia-Linde FE, Wang Y, Higgins ST, Kong KL, et al. Reducing fetal origins of childhood obesity through maternal smoking cessation during pregnancy: an intervention study. Int J Obes (Lond) 2019; 43(7): 1435-9.
Demirhan O, Demir C, Tunç E, Nandıklıoğlu N, Sütcü E, Sadıkoğlu N, et al. The genotoxic effect of nicotine on chromosomes of human fetal cells: the first report described as an important study. Inhal Toxicol 2011; 23(13): 829-34.
Khalil R, Ali D, Al bsoul E, Ghanayem R, Ghanayem R. The effect of waterpipe smoking on DNA integrity among youth in Jordan. Arabian Journal for Science and Engineering 2019; 44(7): 6253-7.
Knopik VS, Maccani MA, Francazio S, McGeary JE. The epigenetics of maternal cigarette smoking during pregnancy and effects on child development. Dev Psychopathol 2012. 24(4): 1377-90.
Rauschert S, Melton PE, Burdge G, Craig JM, Godfrey KM, Holbrook JD, et al. Maternal smoking during pregnancy induces persistent epigenetic changes into adolescence, independent of postnatal smoke exposure and is associated with cardiometabolic risk. Front Genet 2019; 10: 770.
Zong D, Liu X, Li J, Ouyang R, Chen P. The role of cigarette smoke-induced epigenetic alterations in inflammation. Epigenetics & Chromatin 2019; 12(1): 65.
Parmar P, Lowry E, Cugliari G, Suderman M, Wilson R, Karhunen V, et al. Association of maternal prenatal smoking GFI1-locus and cardio-metabolic phenotypes in 18,212 adults. EBioMedicine 2018; 38: 206-16.
Hackshaw A, Rodeck C, Boniface S. Maternal smoking in pregnancy and birth defects: a systematic review based on 173 687 malformed cases and 11.7 million controls. Hum Reprod Update 2011; 17(5): 589-604.
Leite M, Albieri V, Kjaer SK, Jensen A. Maternal smoking in pregnancy and risk for congenital malformations: results of a Danish register‐based cohort study. Acta Obstet Gynecol Scand 2014; 93(8): 825-34.
Perry MF, Mulcahy H, de Franco EA. Influence of periconception smoking behavior on birth defect risk. Am J Obstetr Gynecol 2019; 220(6): 588.e1-588.e7.
Jiang XY, Feng YL, Ye LT, Li XH, Feng J, Zhang MZ, et al., Inhibition of Gata4 and Tbx5 by nicotine-mediated DNA methylation in myocardial differentiation. Stem Cell Reports 2017; 8(2): 290-304.
Lie RT, Wilcox AJ, Taylor J, Gjessing HK, Saugstad OD, Aabyholm F, et al. Maternal smoking and oral clefts: the role of detoxification pathway genes. Epidemiology 2008; 19(4): 606-15.
Xuan Z, Zhongpeng Y, Yanjun G, Jiaqi D, Yuchi Z, Bing S, et al. Maternal active smoking and risk of oral clefts: a meta-analysis. Oral Surg Oral Med Oral Pathol Oral Radiol 2016; 122(6): 680-90.
Honein MA, Paulozzi LJ, Moore CA. Family history, maternal smoking, and clubfoot: an indication of a gene-environment interaction. Am J Epidemiol 2000; 152(7): 658-65.
Stroud LR, McCallum M, Salisbury A. Impact of maternal prenatal smoking on fetal to infant neurobehavioral development. Dev Psychopathol 2018; 30(3): 1087-105.
McClernon FJ, Kollins SH. ADHD and smoking: from genes to brain to behavior. Ann N Y Acad Sci 2008; 1141: 131-47.
Al-Bashaireh AM, Haddad LG, Weaver M, Kelly DL, Chengguo X, Yoon S. The effect of tobacco smoking on musculoskeletal health: a systematic review. J Environ Public Health 2018: 2018.
Alihoseini, H. (2020). Effects of Smoking on the Health of Children from Embryonic Period to Adulthood: A Review Article. World Journal of Peri and Neonatology, 3(1), 19-27. doi: 10.18502/wjpn.v3i1.5062
MLA
Haniye Alihoseini. "Effects of Smoking on the Health of Children from Embryonic Period to Adulthood: A Review Article", World Journal of Peri and Neonatology, 3, 1, 2020, 19-27. doi: 10.18502/wjpn.v3i1.5062
HARVARD
Alihoseini, H. (2020). 'Effects of Smoking on the Health of Children from Embryonic Period to Adulthood: A Review Article', World Journal of Peri and Neonatology, 3(1), pp. 19-27. doi: 10.18502/wjpn.v3i1.5062
VANCOUVER
Alihoseini, H. Effects of Smoking on the Health of Children from Embryonic Period to Adulthood: A Review Article. World Journal of Peri and Neonatology, 2020; 3(1): 19-27. doi: 10.18502/wjpn.v3i1.5062