Evidence of an association between mannose binding lectin codon 54 polymorphism and adenoidectomy and/or tonsillectomy in children

Int J Pediatr Otorhinolaryngol. 2007 Aug;71(8):1157-61. doi: 10.1016/j.ijporl.2007.05.004. Epub 2007 Jun 7.

Abstract

Mannose binding lectin (MBL) is a calcium-dependent lectin that plays an important role innate immunity by activating the complement pathway. There have been a number of studies describing an association between the MBL genotype and disease susceptibility. MBL deficiency has been described as one of the factors leading to a number of infections in children with recurrent upper respiratory tractus infections (URTI). We hypothesized that MBL deficiency may be associated with recurrent URTI, which requires adenoidectomy and/or adenotonsillectomy. In this study to clarify this hypothesis we investigated whether there may be an association between two low producing MBL variants and adenoidectomy and/or tonsillectomy due to recurrent URTI in children. Blood samples were collected, adenoidectomy and/or tonsillectomy due to recurrent URTI and 50 controls (mean age 80.53 +/- 32.62 months). In all patients and controls codon 54 and codon 57 polymorphisms of the MBL gene were analyzed. None of the subjects from the patient group and control group carried codon 57 polymorphism of the MBL gene. The frequency of low-level MBL genotypes (AB and BB) for codon 54 polymorphism in the patient group was found to be significantly higher compared to the control subjects (55.7% versus 14%) (p<0.001). This study shows that the presence of low-level MBL alleles is associated with adenoidectomy and/or tonsillectomy caused by recurrent URTI in children.

MeSH terms

  • Adenoidectomy*
  • Alleles
  • Child
  • Codon
  • DNA Fragmentation
  • Disease Susceptibility
  • Exons
  • Female
  • Genotype
  • Humans
  • Male
  • Mannose-Binding Lectin / deficiency
  • Mannose-Binding Lectin / genetics*
  • Polymerase Chain Reaction
  • Polymorphism, Genetic*
  • Recurrence
  • Respiratory Tract Infections / genetics*
  • Respiratory Tract Infections / metabolism
  • Respiratory Tract Infections / surgery
  • Tonsillectomy*

Substances

  • Codon
  • MBL2 protein, human
  • Mannose-Binding Lectin