Association of Genetic Variants of NLRP4 with Exacerbation of Asthma: The Effect of Smoking

DNA Cell Biol. 2019 Jan;38(1):76-84. doi: 10.1089/dna.2018.4433. Epub 2018 Dec 8.

Abstract

Asthma exacerbation is induced by the interaction of genes and environmental factors such as cigarette smoke. NLRP4 counteracts the activity of the inflammasome, which is responsible for asthma exacerbation. In this study, we analyzed the association of single-nucleotide polymorphisms of NLRP4 with the annual rate of exacerbation and evaluated the additive effect of smoking in 1454 asthmatics. Asthmatics possessing the minor allele of rs1696718G > A had more frequent exacerbation episodes than those homozygous for the common allele (0.59 vs. 0.36/year) and the association was present only in current and ex-smokers. There was a significant interaction between the amount smoked and rs16986718 genotypes (p = 0.014) and a positive correlation between the number of annual exacerbation episodes and amount smoked only in rs16986718G > A AA homozygotes. The prevalence of frequent exacerbators (≥2 exacerbation episodes/year) was 2.5 times higher in rs16986718G > A minor allele homozygotes than in common allele homozygotes (12.0% vs. 5.9%). Furthermore, the prevalence was 6 times higher in rs16986718G > A minor allele homozygotes who were current and ex-smokers than in nonsmokers (25.6% vs. 4.1%). The minor allele of rs16986718G > A in NLRP4 may be a genetic marker that predicts asthma exacerbation in adult asthmatics who smoke.

Keywords: NLRP4; asthma; exacerbation; gene-environment interaction; inflammasome; single nucleotide polymorphism; smoking.

MeSH terms

  • Adaptor Proteins, Signal Transducing
  • Adult
  • Alleles
  • Asthma / epidemiology
  • Asthma / etiology
  • Asthma / genetics*
  • Female
  • Gene-Environment Interaction
  • Genetic Variation
  • Genotype
  • Humans
  • Male
  • Middle Aged
  • Polymorphism, Single Nucleotide
  • Prevalence
  • Repressor Proteins / genetics*
  • Smoking / adverse effects*
  • Young Adult

Substances

  • Adaptor Proteins, Signal Transducing
  • NLRP4 protein, human
  • Repressor Proteins