AHR rs4410790 genotype and IgG levels: Effect modification by lifestyle factors

PLoS One. 2023 Oct 2;18(10):e0290700. doi: 10.1371/journal.pone.0290700. eCollection 2023.

Abstract

Inflammation is a multifaceted marker resulting from complex interactions between genetic and lifestyle factors. Emerging evidence suggests Aryl hydrocarbon receptor (AHR) protein may be implicated in the regulation of immune system and inflammatory responses. To investigate whether rs4410790 genotype (TT, TC, CC) near AHR gene is related to serum IgG levels, a marker of chronic inflammation, and whether lifestyle factors modifies the relationship, we conducted a cross-sectional study by recruiting 168 Korean adults. Participants responded to a lifestyle questionnaire and provided oral epithelial cells and blood samples for biomarker assessment. Among these participants, C allele was the minor allele, with the minor allele frequency of 40%. The rs4410790 TT genotype was significantly associated with elevated IgG levels compared with TC/CC genotypes, after adjusting for potential confounders (p = 0.04). The relationship varied significantly by levels of alcohol consumption (P interaction = 0.046) and overweight/obese status (P interaction = 0.02), but not by smoking status (P interaction = 0.64) and coffee consumption (P interaction = 0.55). Specifically, higher IgG levels associated with the TT genotype were evident in frequent drinkers and individuals with BMI≥23kg/m2, but not in their counterparts. Thus, rs4410790 genotype may be associated with IgG levels and the genetic predisposition to higher IgG levels may be mitigated by healthy lifestyle factors like infrequent drinking and healthy weight.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Alcohol Drinking*
  • Cross-Sectional Studies
  • Genotype
  • Humans
  • Immunoglobulin G / genetics
  • Inflammation / genetics
  • Life Style
  • Polymorphism, Single Nucleotide
  • Receptors, Aryl Hydrocarbon* / genetics

Substances

  • Immunoglobulin G
  • Receptors, Aryl Hydrocarbon
  • AHR protein, human

Grants and funding

JK was supported by the BK21-plus education program from the National Research Foundation of Korea. NK was supported by funding from the National Research Foundation of Korea (NRF-2018R1C1B6008822). YK was supported by funding from MSIT and MOHW (2021M3E5E5096464), MOE (2022R1A6A1A03053343), and MOTIE (S2021A043800034) of Korea. DHL was supported by the Yonsei University Research Fund of 2023-22-0159. SK was supported by Cooperative Research Program for Agriculture Science and Technology Development (Project No. PJ01669005) from Rural Development Administration.