Rapid Detection of the Three Celiac Disease Risk Genotypes HLA-DQ2.2, HLA-DQ2.5, and HLA-DQ8 by Multiplex Ligation-Dependent Probe Amplification

Genet Test Mol Biomarkers. 2016 Mar;20(3):158-61. doi: 10.1089/gtmb.2015.0233. Epub 2016 Jan 22.

Abstract

Background: Genotyping of HLA-DQ2.2, HLA-DQ2.5, and HLA-DQ8 is important in celiac disease (CD). The absence of these three genotypes has a strong negative predictive value.

Methods: We designed multiplex ligation-dependent probe amplification (MLPA) for the combined detection of HLA-DQ2.2, HLA-DQ2.5, and HLA-DQ8. The MLPA probe mix was validated against a set of 59 samples characterized by conventional techniques.

Results: The MLPA assay genotyped all 59 samples correctly when compared to the results obtained by PCR-SSCP/HD or PCR-SSO and PCR-SSP.

Conclusion: The MLPA assay provides a reliable single-reaction analysis of the CD risk genotypes HLA-DQ2.2, HLA-DQ2.5, and HLA-DQ8 allowing for stratification or exclusion of disease risk.

MeSH terms

  • Alleles
  • Celiac Disease / blood
  • Celiac Disease / genetics*
  • Gene Frequency / genetics
  • Genetic Predisposition to Disease
  • Genotype
  • HLA-DQ Antigens / blood
  • HLA-DQ Antigens / genetics*
  • Haplotypes
  • Humans
  • Multiplex Polymerase Chain Reaction / methods
  • Risk Factors

Substances

  • HLA-DQ Antigens
  • HLA-DQ2 antigen
  • HLA-DQ8 antigen