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Fetal lipidome and incident risk of food allergy: A prospective birth cohort study
Xiumei Hong1, Liming Liang2, Hongkai Ji3
1Center on the Early Life Origins of Disease, Department of Population, Family and Reproductive Health, Johns Hopkins University Bloomberg School of Public Health, Baltimore, Maryland, USA.
Insights
Specific long-chain triacylglycerols in newborns are linked to a lower risk of developing food allergies. Combined maternal and infant levels show an additive protective effect, suggesting potential biomarkers for early detection.
Area of Science:
- Immunology
- Metabolomics
- Pediatrics
Background:
- Lipids play a role in adaptive immunity and allergy development, but findings are inconsistent.
- Understanding the newborn lipidome's impact on food allergy (FA) risk is crucial.
Purpose of the Study:
- To investigate the association between the newborn lipidome and the risk of developing food allergy (FA).
- To explore the combined effects of maternal and cord blood lipid metabolites on FA development.
Main Methods:
- Analyzed 202 lipid metabolites in cord plasma from 647 mother-child pairs.
- Utilized liquid chromatography tandem mass spectrometry for lipid profiling.
- Applied logistic regression to assess relationships between metabolites and FA risk.
Main Results:
- Found that specific cord triacylglycerols (long carbon chains, multiple double bonds) were associated with decreased FA risk.
- Observed an additive protective effect of maternal and cord blood triacylglycerols on FA risk.
- Children with high levels of C56:8 triacylglycerol in both maternal and cord plasma had the lowest FA risk (OR=0.24).
Conclusions:
- This is the first birth cohort study linking cord plasma lipidome to childhood FA risk.
- Suggests triacylglycerols with long carbon chains and multiple double bonds as potential predictive biomarkers for FA.
- Highlights the need for further research into triacylglycerols as therapeutic targets for food allergy.
Background:
Lipids are proposed to be important in developing adaptive immunity and allergy. However, studies to date reported inconsistent findings.
Objective:
To examine newborn lipidome (a comprehensive profiling of circulating lipid metabolites) on child's risk of developing food allergy (FA). The maternal-cord joint effects of lipid metabolites on FA development were also investigated.
Methods:
This study included 647 mother-child pairs from the Boston Birth Cohort and analyzed 202 lipid metabolites in cord plasma profiled by liquid chromatography tandem mass spectrometry. FA was defined based on standard clinical criteria. Logistic regression was applied to examine the relationships between individual metabolites and risk of FA.
Results:
Of the 647 children, 61 developed FA. Cord triacylglycerols of long carbon chains and multiple double bonds were significantly associated with decreased risk of FA. These associations were comparable across strata of pertinent maternal and child covariates, and were independent of maternal triacylglycerols when assessed simultaneously. Besides, cord and maternal triacylglycerols had an additive effect in association with risk of FA: Children having high (≥Median) C56:8 triacylglycerol levels in both cord and maternal plasma were at the lowest risk of developing FA (OR = 0.24, 95% CI = 0.10-0.56, p = .001), compared to those having low levels in both cord and maternal plasma.
Conclusion:
This is the first birth cohort study to link altered cord plasma lipidome with future risk of development FA during childhood. It calls for further investigation on triacylglycerols of long carbon chains and multiple double bonds as potential novel predictive biomarkers and therapeutic targets for FA.
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