Polymorphisms in the interleukin-1 gene cluster in children and young adults with systemic meningococcemia.

نویسندگان

  • Georg Endler
  • Rodrig Marculescu
  • Philipp Starkl
  • Alexander Binder
  • Gotho Geishofer
  • Martin Müller
  • Bettina Zöhrer
  • Bernhard Resch
  • Werner Zenz
  • Christine Mannhalter
چکیده

BACKGROUND An association has been described between mortality in children with meningococcal disease and functional polymorphisms in the interleukin-1 (IL1) cluster. We undertook a multicenter study to evaluate associations of these polymorphisms in a Central European population. PATIENTS AND METHODS The study involved 95 Middle European pediatric hospitals. We collected blood samples from, and clinical information about, 285 previously healthy children with meningococcal infection. We used a newly developed multiplexed mutagenic separated PCR assay to analyze 6 polymorphisms within the IL1 cluster: IL1A (-889)C/T, IL1A (+4845)G/T, IL1B (-511)C/T, IL1B (-31)C/T, IL1B (+3954), and IL1RA (+2018)C/T. We studied the same polymorphisms in a comparison group of 481 healthy newborns. RESULTS Genotype frequencies between patients and the comparison group differed significantly only for the IL1RA (+2018)C/T variant: The CC genotype was more frequent in patients (11%) than in healthy controls (5%; P = 0.008). In the patient group, the C allele was significantly more prevalent (67%) in nonsurvivors than in survivors (42%; P = 0.02). CONCLUSION The IL1RA (+2018)C/T polymorphism is associated with the risk of meningococcal disease and with its outcome.

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عنوان ژورنال:
  • Clinical chemistry

دوره 52 3  شماره 

صفحات  -

تاریخ انتشار 2006