Association of CD14 genetic variants and circulating level with systemic lupus erythematosus risk in Egyptian children and adolescents

Biomark Med. 2021 Dec;15(17):1669-1680. doi: 10.2217/bmm-2021-0203. Epub 2021 Nov 8.

Abstract

Aim: To demonstrate whether sCD14 and CD14 (rs2569190 A/G and rs2569191 C/T) genetic variants are associated with systemic lupus erythematosus (SLE) risk, for the first time, in Egyptian pediatrics and adolescents. Materials & methods: sCD14 concentrations were determined in plasma of 95 SLE cases and 98 healthy controls using ELISA assay. Genotyping was performed using TaqMan technology. Results: sCD14 levels were elevated in SLE. Individuals with T, CT and TT genotypes in rs2569191 were of significant risk (odds ratio = 1.471-2.035, 95% CI = 1.138-3.471) and those with combined CT+TT and haplotype GT were of higher risk of SLE (odds ratio = 1.660-1.758, 95% CI = 1.003-3.106, p < 0.05). sCD14 levels and CD14 polymorphism were not correlated with SLE clinical and laboratory features. Conclusion: In SLE, sCD14 levels are associated with rs2569190 A/G. Genotype CT+TT in rs2569191 C/T and haplotype GT are associated with SLE risk in Egyptian pediatric and adolescents.

Keywords: autoantibodies; genotype; haplotype; inflammatory; innate immunity; polymorphism.

MeSH terms

  • Adolescent
  • Alleles
  • Child
  • Child, Preschool
  • Egypt
  • Female
  • Gene Frequency
  • Genetic Association Studies*
  • Genetic Predisposition to Disease*
  • Haplotypes / genetics
  • Humans
  • Lipopolysaccharide Receptors / blood*
  • Lipopolysaccharide Receptors / genetics*
  • Lupus Erythematosus, Systemic / blood*
  • Lupus Erythematosus, Systemic / genetics*
  • Lupus Erythematosus, Systemic / immunology
  • Male
  • Multivariate Analysis
  • Polymorphism, Single Nucleotide / genetics*
  • ROC Curve
  • Regression Analysis
  • Risk Factors

Substances

  • CD14 protein, human
  • Lipopolysaccharide Receptors