4.7 Article

Unconjugated bilirubin is associated with protection from early-life wheeze and childhood asthma

期刊

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
卷 148, 期 1, 页码 128-138

出版社

MOSBY-ELSEVIER
DOI: 10.1016/j.jaci.2020.12.639

关键词

Wheeze; asthma; metabolomics; bilirubin; lipid mediators

资金

  1. National Institutes of Health (NIH) [UG3 OD023282, UL1 TR002373, UM1AI114271, U19AI095230, K24 AI 077930, T32 HL087738, K12 HD04348318, K01HL149989]
  2. Childhood Origins of Asthma Study [P01 HL070831, U10 HL064305, R01 HL061879]
  3. Infant Susceptibility to Pulmonary Infections and Asthma following RSV Exposure [U19 AI 095227, UL1 RR 024975, R21 HD087864]
  4. Wisconsin Infant Study Cohort [2U19AI104317]

向作者/读者索取更多资源

This study identified a novel inverse, dose-dependent association between plasma levels of Z,Z unconjugated bilirubin (UCB) and related metabolites with early-life wheeze and childhood asthma, along with significant negative correlations with inflammatory lipid mediators and oxidative stress byproducts.
Background: Wheeze and allergic sensitization are the strongest early-life predictors of childhood asthma development; the molecular origins of these early-life phenotypes are poorly understood. Objectives: We sought to identify metabolites associated with early-life wheeze, allergic sensitization, and childhood asthma. Methods: We conducted a nested case-control study using Environmental influences on Child Health Outcomes Program cohorts for discovery and independent replication. Wheeze and allergic sensitization were defined by number of wheeze episodes and positive specific IgE at age 1 year, respectively. Asthma was defined as physician diagnosis of asthma at age 5 or 6 years. We used untargeted metabolomics, controlling for observed and latent confounding factors, to assess associations between the plasma metabolome and early-life wheeze, allergy, and childhood asthma. Results: Eighteen plasma metabolites were associated with first year wheeze in the discovery cohort (n = 338). Z,Z unconjugated bilirubin (UCB) and its related metabolites exhibited a dose-response relationship with wheeze frequency; UCB levels were 13% (beta = 0.87; 95% CI, 0.74-1.02) and 22% (beta = 0.78; 95% CI, 0.68-0.91) lower in children with 1 to 3 and 41 wheeze episodes compared with those who never wheezed, respectively. UCB levels were also associated with childhood asthma (beta = 0.82; 95% CI, 0.68-0.98). Similar trends were observed in 2 independent cohorts. UCB was significantly negatively correlated with eicosanoid- and oxidative stress-related metabolites. There were no significant associations between metabolites and allergic sensitization. Conclusions: We identified a novel inverse, dose-dependent association between UCB and recurrent wheeze and childhood asthma. Inflammatory lipid mediators and oxidative stress byproducts inversely correlated with UCB, suggesting that UCB modulates pathways critical to the development of early-life recurrent wheeze and childhood asthma.

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