PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
June 3, 2026BMC Pediatrics1 citationsOpen Access

Early life factors and genetic interactions in allergic rhinitis: a genome-wide study

HHuangZZZiyan ZhangHZHongting Zhang

Key Points

  • This study aims to explore how early life factors and genetic interactions contribute to the risk of allergic rhinitis.
  • Utilized cross-sectional data from the UK Biobank and West China Hospital to analyze early life factors and allergic rhinitis associations.
  • Performed multivariable logistic regression and a genome-wide gene-environment interaction study (GWGEIS) to assess risks.
  • Assessed nine early life factors, including long-term antibiotic usage and cesarean delivery, in relation to allergic rhinitis.
  • Long-term/recurrent antibiotic usage associated with AR (UKB: OR = 1.49, P < 0.001; WCH: OR = 2.18, P < 0.001).
  • Cesarean delivery linked to higher AR risk (UKB: OR = 1.26, P = 0.0014; WCH: OR = 1.47, P = 0.008), especially in females under 16.
  • Identified significant association between ATE1 gene interaction and LTRAU (rs4752620, P = 2.51E-8).

Abstract

Early life factors play an important role in the development and progression of allergic rhinitis (AR), but their relationship and underlying genetic mechanisms still remains unclear. Using cross-sectional data from the UK Biobank (UKB) and West China Hospital (WCH), we assessed the associations between nine early life factors—birth weight, body size and height at age 10, multiple births, maternal smoking around birth, breastfeeding, long-term/recurrent antibiotic usage as a child or teenager (LTRAU), cesarean delivery, and maternal age—and the development of AR through multivariable logistic regression models. We also conducted a genome-wide gene-environment interaction study (GWGEIS) to explore the correlation between polygenic risk scores (PRS) derived from GWGEIS and AR risk. In both UKB and WCH cohorts, LTRAU (UKB cohort: OR = 1.49, P < 0.001; WCH cohort: OR = 2.18, P < 0.001), and born by cesarean delivery (UKB cohort: OR = 1.26, P = 0.0014; WCH cohort: OR = 1.47, P = 0.008) were identified as independent risk factors for AR. Notably, the association between cesarean delivery and an increased risk of AR was confined to female offspring who developed AR before the age of 16. In contrast, the detrimental effects of LTRAU remained significant in offspring who developed AR after the age of 16. Additionally, GWGEIS identified an interaction between the ATE1 gene and LTRAU (rs4752620, P = 2.51E-8, β = -0.30). Furthermore, the PRS derived from GWGEIS results was significantly associated with the risk of AR (OR = 1.06, P = 0.038). These findings enhance our understanding of how early life factors, particularly LTRAU, and genetic factors synergistically affect AR risk, offering valuable insights for prevention and treatment strategies.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Huang et al. (2026) studied this question.

synapsesocial.com/papers/6a1fc509dee9eb8c0dce6849https://doi.org/10.1186/s12887-026-07052-6
Ask AI
Helpful
Bookmark
Share
View Full Paper