ADA genetic polymorphism and the effect of smoking on neonatal bilirubinemia and developmental parameters

Early Hum Dev. 2008 Nov;84(11):739-43. doi: 10.1016/j.earlhumdev.2008.05.001. Epub 2008 Jun 17.

Abstract

Background: Genetic variability of metabolic enzymes may influence the effect of cigarette smoking on intrauterine development and on early neonatal events.

Aims: To investigate the role of adenosine deaminase genetic polymorphism on the effect of smoking on neonatal bilirubinemia and developmental parameters.

Study design: Analysis of association between adenosine deaminase phenotypes and neonatal developmental parameters. Prospective study of serum bilirubin level in relation to adenosine deaminase phenotype.

Methods: We have studied 360 consecutive newborn infants from the Caucasian population of Rome. Serum bilirubin concentration was determined at birth and every 24 h for the first five days.

Results: Overall maternal smoking is associated with a slight decrease in the incidence of phototherapy (13.4% in non smoking vs 11.7% in smoking mothers) and with a reduction of birth weight (3374 g in non smoking mothers vs 3133 g in smoking mothers). There is a significant interaction between smoke and adenosine deaminase. While in non smoking mothers the incidence of phototherapy in carriers of ADA 2 allele is higher than in ADA 1 phenotype, in infants from smoking mothers the pattern is reversed and the incidence of phototherapy in carriers of ADA 2 allele is lower than in infants with ADA 1 phenotype. Other neonatal bilirubin parameters follow a similar pattern of interaction between smoking and ADA. The negative effect of smoke on birth weight is much more evident in infant with ADA 1 phenotype than in those carrying the ADA 2 allele.

Conclusions: The data suggest that ADA phenotype modifies the effect of smoking on developmental and bilirubin parameters.

MeSH terms

  • Adenosine Deaminase / genetics*
  • Adenosine Deaminase / metabolism
  • Alleles
  • Bilirubin / blood*
  • Birth Weight
  • Electrophoresis, Starch Gel
  • Female
  • Genetic Variation
  • Gestational Age
  • Humans
  • Hyperbilirubinemia, Neonatal / blood
  • Hyperbilirubinemia, Neonatal / enzymology
  • Hyperbilirubinemia, Neonatal / genetics
  • Infant, Newborn / blood*
  • Isoenzymes
  • Phenotype
  • Polymorphism, Genetic
  • Pregnancy
  • Prospective Studies
  • Smoking / adverse effects*

Substances

  • Isoenzymes
  • Adenosine Deaminase
  • Bilirubin