Mannose-binding lectin serum levels and (Gly54asp) gene polymorphism in recurrent aphthous stomatitis: A case-control study

Int J Immunopathol Pharmacol. 2021 Jan-Dec:35:20587384211064454. doi: 10.1177/20587384211064454.

Abstract

Objectives: Dysregulation of the immune response appears to play a significant role in recurrent aphthous stomatitis (RAS) development. The main objective of this case-control study is to investigate the blood levels of mannose-binding lectin (MBL) and the frequency of the MBL2 gene (gly54asp) polymorphism in RAS patients, including 40 RAS patients and 40 healthy controls. Methods: Serum MBL levels were determined by ELISA, while the PCR-restriction fragment length polymorphism was used in MBL2 genotyping. Results: The median serum MBL level was significantly lower in the RAS group than in the control group (975 ng/mL (545-1320) vs. 1760 ng/mL (1254-2134); p≤ 0.001). The MBL levels were significantly lower in the BB genotype, whereas they were significantly higher in the wild type AA with a median of 525 and 1340 ng/mL, respectively (p =0.005). The B allele was expressed in significantly higher percentages of RAS patients than in controls. There was no significant association between MBL serum levels (p=0.685) or MBL2 codon 54 genotypes (p=0.382) with the type of ulcers. Conclusion: There was an association between low MBL serum levels and the variant allele B of the MBL2 (gly54asp) gene, and the susceptibility to RAS. As a result, potential novel therapeutic options for RAS patients with MBL deficiency should be investigated.

Keywords: Codon 54; mannose binding lectin; oral ulcer; polymorphism; recurrent aphthous stomatitis.

MeSH terms

  • Adult
  • Case-Control Studies
  • Egypt / epidemiology
  • Female
  • Gene Frequency
  • Genetic Predisposition to Disease
  • Genotyping Techniques / methods
  • Genotyping Techniques / statistics & numerical data
  • Humans
  • Male
  • Mannose-Binding Lectin / blood*
  • Mannose-Binding Lectin / deficiency*
  • Mannose-Binding Lectin / genetics
  • Metabolism, Inborn Errors* / diagnosis
  • Metabolism, Inborn Errors* / genetics
  • Metabolism, Inborn Errors* / physiopathology
  • Polymorphism, Single Nucleotide
  • Stomatitis, Aphthous* / blood
  • Stomatitis, Aphthous* / diagnosis
  • Stomatitis, Aphthous* / genetics
  • Stomatitis, Aphthous* / therapy

Substances

  • MBL2 protein, human
  • Mannose-Binding Lectin

Supplementary concepts

  • Mannose-Binding Protein Deficiency
  • Sutton disease 2