Your browser doesn't support javascript.
loading
Prenatal parental tobacco smoking, gene specific DNA methylation, and newborns size: the Generation R study.
Bouwland-Both, Marieke I; van Mil, Nina H; Tolhoek, Catharina P; Stolk, Lisette; Eilers, Paul H C; Verbiest, Michael M P J; Heijmans, Bastiaan T; Uitterlinden, André G; Hofman, Albert; van Ijzendoorn, Marinus H; Duijts, Liesbeth; de Jongste, Johan C; Tiemeier, Henning; Steegers, Eric A P; Jaddoe, Vincent W V; Steegers-Theunissen, Régine P M.
Afiliação
  • Bouwland-Both MI; The Generation R Study Group, Erasmus MC, University Medical Centre Rotterdam, Rotterdam, The Netherlands ; Department of Obstetrics and Gynecology, Erasmus MC, University Medical Centre, Ee-building Room 2271a, PO Box 1738, 3000 DR Rotterdam, The Netherlands.
  • van Mil NH; The Generation R Study Group, Erasmus MC, University Medical Centre Rotterdam, Rotterdam, The Netherlands ; Department of Obstetrics and Gynecology, Erasmus MC, University Medical Centre, Ee-building Room 2271a, PO Box 1738, 3000 DR Rotterdam, The Netherlands ; Department of Child and Adolescent Psy
  • Tolhoek CP; The Generation R Study Group, Erasmus MC, University Medical Centre Rotterdam, Rotterdam, The Netherlands ; Department of Obstetrics and Gynecology, Erasmus MC, University Medical Centre, Ee-building Room 2271a, PO Box 1738, 3000 DR Rotterdam, The Netherlands.
  • Stolk L; Department of Internal Medicine, Erasmus MC, University Medical Centre, Rotterdam, The Netherlands.
  • Eilers PH; Department of Biostatistics, Erasmus MC, University Medical Centre, Rotterdam, The Netherlands.
  • Verbiest MM; Department of Internal Medicine, Erasmus MC, University Medical Centre, Rotterdam, The Netherlands.
  • Heijmans BT; Department of Molecular Epidemiology, Leiden University Medical Centre, Leiden, The Netherlands.
  • Uitterlinden AG; Department of Internal Medicine, Erasmus MC, University Medical Centre, Rotterdam, The Netherlands ; Department of Epidemiology, Erasmus MC, University Medical Centre, Rotterdam, The Netherlands.
  • Hofman A; Department of Epidemiology, Erasmus MC, University Medical Centre, Rotterdam, The Netherlands.
  • van Ijzendoorn MH; School for Pedagogical and Educational Sciences, Erasmus MC, University Medical Centre, Rotterdam, The Netherlands.
  • Duijts L; Department of Epidemiology, Erasmus MC, University Medical Centre, Rotterdam, The Netherlands ; Department of Pediatrics, Erasmus Medical Center, Rotterdam, The Netherlands.
  • de Jongste JC; Department of Pediatrics, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Tiemeier H; Department of Child and Adolescent Psychiatry/Psychology, Erasmus MC, University Medical Centre, Rotterdam, The Netherlands ; Department of Epidemiology, Erasmus MC, University Medical Centre, Rotterdam, The Netherlands.
  • Steegers EA; Department of Obstetrics and Gynecology, Erasmus MC, University Medical Centre, Ee-building Room 2271a, PO Box 1738, 3000 DR Rotterdam, The Netherlands.
  • Jaddoe VW; The Generation R Study Group, Erasmus MC, University Medical Centre Rotterdam, Rotterdam, The Netherlands ; Department of Epidemiology, Erasmus MC, University Medical Centre, Rotterdam, The Netherlands.
  • Steegers-Theunissen RP; Department of Obstetrics and Gynecology, Erasmus MC, University Medical Centre, Ee-building Room 2271a, PO Box 1738, 3000 DR Rotterdam, The Netherlands.
Clin Epigenetics ; 7: 83, 2015.
Article em En | MEDLINE | ID: mdl-26265957
BACKGROUND: Deleterious effects of prenatal tobacco smoking on fetal growth and newborn weight are well-established. One of the proposed mechanisms underlying this relationship is alterations in epigenetic programming. We selected 506 newborns from a population-based prospective birth cohort in the Netherlands. Prenatal parental tobacco smoking was assessed using self-reporting questionnaires. Information on birth outcomes was obtained from medical records. The deoxyribonucleic acid (DNA) methylation of the growth genes IGF2DMR and H19 was measured in newborn umbilical cord white blood cells. Associations were assessed between parental tobacco smoking and DNA methylation using linear mixed models and adjusted for potential confounders. RESULTS: The DNA methylation levels of IGF2DMR and H19 in the non-smoking group were median (90 % range), 54.0 % (44.6-62.0), and 30.0 % (25.5-34.0), in the first trimester only smoking group 52.2 % (44.5-61.1) and 30.8 % (27.1-34.1), and in the continued smoking group 51.6 % (43.9-61.3) and 30.2 % (23.7-34.8), respectively. Continued prenatal maternal smoking was inversely associated with IGF2DMR methylation (ß = -1.03, 95 % CI -1.76; -0.30) in a dose-dependent manner (P-trend = 0.030). This association seemed to be slightly more profound among newborn girls (ß = -1.38, 95 % CI -2.63; -0.14) than boys (ß = -0.72, 95 % CI -1.68; 0.24). H19 methylation was also inversely associated continued smoking <5 cigarettes/day (ß = -0.96, 95 % CI -1.78; -0.14). Moreover, the association between maternal smoking and newborns small for gestational age seems to be partially explained by IGF2DMR methylation (ß = -0.095, 95 % CI -0.249; -0.018). Among non-smoking mothers, paternal tobacco smoking was not associated with IGF2DMR or H19 methylation. CONCLUSIONS: Maternal smoking is inversely associated with IGF2DMR methylation in newborns, which can be one of the underlying mechanisms through which smoking affects fetal growth.
Palavras-chave

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: Clin Epigenetics Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Holanda

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: Clin Epigenetics Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Holanda