Supplementary Material for: UGT1A1*28 Genotypes and Respiratory Disease in Very Preterm Infants: A Cohort Study

  • Jesper Padkaer Petersen (Ophavsperson)
  • Finn Ebbesen (Ophavsperson)
  • Mads Vilhelm Hollegaard (Ophavsperson)
  • Sofia Andersson (Ophavsperson)
  • David Michael Hougaard (Ophavsperson)
  • Ole Thorlacius-Ussing (Ophavsperson)
  • Tine Brink Henriksen (Aarhus University) (Ophavsperson)

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Beskrivelse

Background: Respiratory disease in the very preterm infant is frequent and often severe. Bilirubin is both a potent neurotoxin and antioxidant, and may have a clinical impact on preterm respiratory disease. The Gilbert genotype, the UGT1A1*28 allele, is the major known genetic cause of variation in bilirubin. Objectives: To study the association between respiratory disease in the very preterm infant and the UGT1A1*28 allele. Methods: This is a cohort study of 1,354 very preterm infants (gestational age
Dato for tilgængelighed2017
ForlagFigshare

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