КУРЕНИЕ МАТЕРИ ВО ВРЕМЯ БЕРЕМЕННОСТИ КАК ФАКТОР РИСКА РАЗВИТИЯ ПЛОДА И РЕБЕНКА

Скачать статью в PDF
Номер журнала: 
8
Год издания: 
2017

И. Кельмансон, доктор медицинских наук, профессор Институт специальной педагогики и психологии Международного университета семьи и ребенка им. Рауля Валленберга, Санкт-Петербург Санкт-Петербургский государственный институт психологии и социальной работы E-mail: iakelmanson@hotmail.com

Неблагоприятные воздействия на эмбрион и плод в критические периоды развития могут иметь стойкие, порой необратимые последствия для ребенка. Данное положение укладывается в так называемую концепцию фетального программирования. Устранение таких воздействий – предпосылка к оптимизации развития плода и ребенка, снижению риска заболеваемости и смертности. Рассматриваются важнейшие негативные последствия для течения беременности, развития плода и ребенка, связанные с курением матери во время беременности.

Ключевые слова: 
акушерство и гинекология
курение
плод
тератогенный эффект
фетальное программирование

Для цитирования
Кельмансон И. КУРЕНИЕ МАТЕРИ ВО ВРЕМЯ БЕРЕМЕННОСТИ КАК ФАКТОР РИСКА РАЗВИТИЯ ПЛОДА И РЕБЕНКА . Врач, 2017; (8): 2-6


It appears your Web browser is not configured to display PDF files. Download adobe Acrobat или click here to download the PDF file.

Список литературы: 
  1. Кельмансон И.А. Перинатология и перинатальная психология / СПб: СпецЛит, 2015.
  2. Chatenoud L., Parazzini F., di Cintio E. et al. Paternal and maternal smoking habits before conception and during the first trimester: relation to spontaneous abortion // Ann. Epidemiol. – 1998; 8: 520–6.
  3. Andres R., Day M. Perinatal complications associated with maternal tobacco use // Semin Neonatol. – 2000; 5: 231–41.
  4. Secker-Walker R., Vacek P., Flynn B. et al. Estimated gains in birth weight associated with reductions in smoking during pregnancy // J. Reprod. Med. – 1998; 43 (11): 967–74.
  5. Кельмансон И.А. Низковесный новорожденный и отсроченный риск кардиореспираторной патологии / СПб: Специальная литература, 1999.
  6. Barker D., Osmond C., Forsén T. Et al. Foetal and childhood growth and asthma in adult life // Acta paediatrica. – 2013; 102 (7): 732–8.
  7. Malmberg L., Pelkonen A., Malmström K. et al. Very low birth weight and respiratory outcome: association between airway inflammation and hyperresponsiveness // Ann. Allergy, Asthma & Immunol. – 2013; 111 (2): 96–101.
  8. Goyal N., Fiks A., Lorch S. Association of late-preterm birth with asthma in young children: practice-based study // Pediatrics. – 2011; 128 (4): 830–8.
  9. Гавалов С.М., Соболева М.К. Критерии «табачного синдрома» у новорожденных // Вопросы охраны материнства и детства. – 1991; 10: 30–3.
  10. Tuthill D., Stewart J., Coles E. et al. Maternal cigarette smoking and pregnancy outcome // Paediatr. Perinat. Epidemiol. – 1999; 13: 245–53.
  11. Haustein К. Cigaret smoking, nicotine and pregnany // Int. J. Clin. Pharmacol. Ther. – 1999; 37: 417–27.
  12. Beaty T., Maestri N, Hetmanski J. et al. Testing for interaction between maternal smoking and TGFA genotype among oral cleft cases born in Maryland 1992–1996 // Cleft Palate Craniofac. J. – 1997; 34: 447–54.
  13. Kallen K. Maternal smoking and craniosynostosis // Teratology. – 1999; 60 (3): 146–50.
  14. Kiely M., Cogan P., Kearney P. et al. Relationship between smoking, dietary intakes and plasma levels of vitamin E and beta-carotene in matched maternal-cord pairs // Int. J. Vitam Nutr. Res. – 1999; 69 (4): 262–7.
  15. Lackmann G., Salzberger U., Tollner U. et al. Metabolites of a tobacco-specific carcinogen in urine from newborns // J. Natl. Cancer Inst. – 1999; 91 (5): 459–65.
  16. Pluth J., Ramsey M., Tucker J. Role of maternal exposures and newborn genotypes on newborn chromosome aberration frequencies // Mutat. Res. – 2000; 465: 101–11.
  17. Breton C., Byun H.-M., Wenten M. et al. Prenatal tobacco smoke exposure affects global and gene-specific DNA methylation // Am. J. Respir. Crit. Care Med. – 2009; 180 (5): 462–7.
  18. Li Y.-F., Langholz B., Salam M. et al. Maternal and grandmaternal smoking patterns are associated with early childhood asthma // CHEST J. – 2005; 127 (4): 1232–41.
  19. Wisborg K., Henriksen T., Obel C. et al. Smoking during pregnancy and hospitalization of the child // Pediatrics. – 1999; 104 (4): 46.
  20. Carroll K., Gebretsadik T., Griffin M. et al. Maternal asthma and maternal smoking are associated with increased risk of bronchiolitis during infancy // Pediatrics. – 2007; 119 (6): 1104–12.
  21. Nuesslein T., Beckers D., Rieger C. Cotinine in meconium indicates risk for early respiratory tract infections // Hum. Exp. Toxicol. – 1999; 18 (4): 283–90.
  22. Ey J., Holberg C., Aldous M. et al. Passive smoke exposure and otitis media in the first year of life. Group Health Medical Associates // Pediatrics. – 1995; 95 (5): 670–7.
  23. Sondergaard C., Henriksen T, Obel C. et al. Smoking during pregnancy and infantile colic // Pediatrics. – 2001; 108 (2): 342–6.
  24. Cochran-Black D., Cowan L., Neas B. The relation between newborn hemoglobin F fractions and risk factors for sudden infant death syndrome // Arch. Pathol. Lab. Med. – 2001; 125 (2): 211–7.
  25. Гавалов С.М., Соболева M.K., Дерягина Л.П. и др. Влияние активного и пассивного курения на течение беременности и становление эритроцитарной системы у детей // Тер. арх. – 1991; 3: 126–30.
  26. Hinz D., Bauer M., Röder S. et al. Cord blood Tregs with stable FOXP3 expression are influenced by prenatal environment and associated with atopic dermatitis at the age of one year // Allergy. – 2012; 67 (3): 380–9.
  27. Macaubas C., De Klerk N., Holt B. et al. Association between antenatal cytokine production and the development of atopy and asthma at age 6 years // Lancet. – 2003; 362 (9391): 1192–7.
  28. Devereux G., Barker R., Seaton A. Antenatal determinants of neonatal immune responses to allergens // Clin. Exp. Allergy. – 2002; 32 (1): 43–50.
  29. Penn A., Rouse R., Horohov D. et al. In utero exposure to environmental tobacco smoke potentiates adult responses to allergen in BALB/c mice // Environmental Health Perspectives. – 2007; 548–55.
  30. Londhe V., Sundar I., Lopez B. et al. Hyperoxia impairs alveolar formation and induces senescence through decreased histone deacetylase activity and up-regulation of p21 in neonatal mouse lung // Pediatric Research. – 2011; 69: 371–7.
  31. Beratis N., Panagoulias D., Varvarigou A. Increased blood pressure in neonates and infants whose mothers smoked during pregnancy // J. Pediatr. – 1996; 128 (6): 806–12.
  32. Morley R., Leeson Payne C., Lister G. et al. Maternal smoking and blood pressure in 7.5 to 8 year old offspring // Arch. Dis. Child. – 1995; 72 (2): 120–4. PMCID: 1511033.
  33. Browne C., Colditz P., Dunster K. Infant autonomic function is altered by maternal smoking during pregnancy // Early Hum. Dev. – 2000; 59 (3): 209–18.
  34. Carlsen K., Jaakkola J., Nafstad P. et al. In utero exposure to cigarette smoking influences lung function at birth // Eur. Respir. J. – 1997; 10 (8): 1774–9.
  35. Håland G., Carlsen K., Sandvik L. et al. Reduced lung function at birth and the risk of asthma at 10 years of age // New Engl. J. Med. – 2006; 355 (16): 1682–9.
  36. Henderson A., Sherriff A., Northstone K. et al. Pre- and postnatal parental smoking and wheeze in infancy: cross cultural differences. Avon Study of Parents and Children (ALSPAC) Study Team, European Longitudinal Study of Pregnancy and Childhood (ELSPAC) Co-ordinating Centre // Eur. Respir. J. – 2001; 18 (2): 323–9.
  37. Sekhon H., Keller J., Proskocil B. et al. Maternal Nicotine Exposure Upregulates Collagen Gene Expression in Fetal Monkey Lung: Association with α7 Nicotinic Acetylcholine Receptors // Am. J. Respir. Cell Mol. Biol. – 2002; 26 (1): 31–41.
  38. Wongtrakool C., Wang N., Hyde D. et al. Prenatal nicotine exposure alters lung function and airway geometry through α7 nicotinic receptors // Am. J. Respir. Cell Mol. Biol. – 2012; 46 (5): 695–702.
  39. Elliot J., Carrol N., Bosco M. et al. Increased airway responsiveness and decreased alveolar attachment points following in utero smoke exposure in the guinea pig // Am. J. Respir. Crit. Care Med. – 2001; 163 (1): 140–4.
  40. Кельмансон И.А. Сон и дыхание детей раннего возраста / СПб: Элби-СПб, 2006.
  41. US Department of Health Human Services. The health consequences of smoking – 50 years of progress: a report of the Surgeon General / Atlanta, GA: US Department of Health and Human Services, Centers for Disease Control and Prevention, National Center for Chronic Disease Prevention and Health Promotion, Office on Smoking and Health, 2014; 17.
  42. Кельмансон И.А. Клинико-физиологические аспекты реакции пробуждения у детей раннего возраста // Физиология человека. – 2013; 39 (6): 72–82.
  43. Elliot J., Vullermin P., Carroll N. et al. Increased airway smooth muscle in sudden infant death syndrome // Am. J. Respir. Crit. Care Med. – 1999; 160 (1): 313–6.
  44. Behm I., Kabir Z., Connolly G. et al. Increasing prevalence of smoke-free homes and decreasing rates of sudden infant death syndrome in the United States: an ecological association study // Tobacco Control. – 2012; 21 (1): 6–11.
  45. Oyemade U., Cole O., Johnson A. et al. Prenatal substance abuse and pregnancy outcomes among African American women // J. Nutr. – 1994; 124 (6 Suppl.): 994–9.
  46. Nugent J., Lester B., Greene S. et al. The effects of maternal alcohol consumption and cigarette smoking during pregnancy on acoustic cry analysis // Child Dev. – 1996; 67 (4): 1806–15.
  47. Pichini S., Garcia-Algar O. In utero exposure to smoking and newborn neurobehavior: how to assess neonatal withdrawal syndrome? // Ther. Drug Monit. – 2006; 28 (3): 288–90.
  48. Fried P., Watkinson B., Dillon R. et al. Neonatal neurological status in a low-risk population after prenatal exposure to cigarettes, marijuana, and alcohol // J. Dev. Behav. Pediatr. – 1987; 8 (6): 318–26.
  49. Kelmanson I., Erman L., Litvina S. Maternal smoking during pregnancy and behavioural characteristics in 2–4-month-old infants // Klin. Pädiatr. – 2002; 214 (6): 359–64.
  50. Obel C., Henriksen T., Hedegaard M. et al. Smoking during pregnancy and babbling abilities of the 8-month-old infant // Paediatr. Perinat. Epidemiol. – 1998; 12 (1): 37–48.
  51. Fried P., Watkinson B. 12- and 24-month neurobehavioural follow-up of children prenatally exposed to marihuana, cigarettes and alcohol // Neurotoxicol. Teratol. – 1988; 10 (4): 305–13.
  52. Kelmanson I. Maternal smoking during pregnancy and sleep problems in 2-month-old infants // Somnologie – Schlafforschung und Schlafmedizin. – 2009; 13 (4): 244–50.
  53. Kelmanson I. Perinatal predictors of sleep disturbances in young infants // Somnologie – Schlafforschung und Schlafmedizin. – 2011; 15 (1): 39–46.
  54. Sexton M., Fox N., Hebel J. Prenatal exposure to tobacco: II. Effects on cognitive functioning at age three // Int. J. Epidemiol. – 1990; 19 (1): 72–7.
  55. Drews C., Murphy C., Yeargin-Allsopp M. et al. The relationship between idiopathic mental retardation and maternal smoking during pregnancy // Pediatrics. – 1996; 97 (4): 547–53.
  56. Chen R., Clifford A., Lang L. et al. Is exposure to secondhand smoke associated with cognitive parameters of children and adolescents?-a systematic literature review // Ann. Epidemiol. – 2013; 23 (10): 652–61.