@article{22808970a0a945388f6d4bfaa4d40567,
title = "Maternal triacylglycerol signature and risk of food allergy in offspring",
abstract = "Background: The prevalence of IgE-mediated food allergy (FA) is increasing worldwide, but the underlying mechanisms are poorly understood. Objective: We sought to examine the role of maternal lipidomic profiles in risk of FA development in offspring and to investigate the potential modification effects by timing of first solid-food introduction. Methods: This report included 1068 mother-child dyads from the Boston Birth Cohort. Maternal lipid metabolites in plasma were assessed by using liquid chromatography tandem mass spectrometry. Food sensitization (FS) was defined as a specific IgE level of 0.35 kU/L or greater to any of the 8 common food allergens determined by using ImmunoCAP. FA was defined based on FS, clinical symptoms, and food avoidance. Logistic regression was applied to analyze associations between maternal metabolites and risk of FS and FA in offspring and to explore potential effect modifications. Results: Of the 1068 children, 411 had FS, and 132 had FA. Among the 209 metabolites, maternal triacylglycerols (TAGs) of shorter carbon chains and fewer double bonds were associated with greater risk of FA, whereas TAGs of longer carbon chains and more double bonds were significantly associated with lower risk of FA in offspring. These associations were stronger in children with delayed solid-food introduction (≥7 months of age) than those with earlier solid-food introduction (P =.010 for interaction between the maternal TAG score and timing of solid-food introduction). No significant association was found for FS. Conclusion: This is the first study to demonstrate a link between maternal TAGs and risk of FA in offspring and potential risk modification by timing of solid-food introduction.",
keywords = "Food allergy, lipidomics, timing of first solid-food introduction, triacylglycerol",
author = "Xiumei Hong and Liming Liang and Qi Sun and Keet, {Corinne A.} and Tsai, {Hui Ju} and Yuelong Ji and Guoying Wang and Hongkai Ji and Clary Clish and Colleen Pearson and You Wang and Wood, {Robert A.} and Hu, {Frank B.} and Xiaobin Wang",
note = "Funding Information: The Boston Birth Cohort (the parent study) was supported in part by March of Dimes PERI grants (20-FY02-56 and 21-FY07-605) and National Institutes of Health (NIH) grants (R21ES011666 and R01HD041702). The follow-up study is supported in part by grants from the Bunning family and their family foundations, Food Allergy Research & Education (FARE), and NIH grants (U01AI090727, R21AI079872, R21HD085556, R01HD041702, and R01HD086013). X.H. is supported by the NICHD (R03HD096136). The Boston Birth Cohort (the parent study) was supported in part by March of Dimes PERI grants ( 20-FY02-56 and 21-FY07-605) and National Institutes of Health (NIH) grants ( R21ES011666 and R01HD041702). The follow-up study is supported in part by grants from the Bunning family and their family foundations, Food Allergy Research & Education (FARE), and NIH grants ( U01AI090727, R21AI079872, R21HD085556, R01HD041702, and R01HD086013). X.H. is supported by the NICHD ( R03HD096136). We gratefully acknowledge the individuals who participated in the studies and contributed to this work. We also thank Ms Tami R. Bartell for her English-language editing. We also would like to acknowledge Linda Rosen and the Clinical Data Warehouse (CDW) for the assistance in obtaining relevant clinical information; CDW service is supported by the Boston University's Clinical and Translational Institute and NIH CTSA grant U54-TR001012. The Boston Birth Cohort (the parent study) was supported in part by March of Dimes PERI grants ( 20-FY02-56 and 21-FY07-605) and National Institutes of Health (NIH) grants ( R21ES011666 and R01HD041702). The follow-up study is supported in part by grants from the Bunning family and their family foundations, Food Allergy Research & Education (FARE), and NIH grants ( U01AI090727, R21AI079872, R21HD085556, R01HD041702, and R01HD086013). X.H. is supported by the NICHD ( R03HD096136). Funding Information: The Boston Birth Cohort (the parent study) was supported in part by March of Dimes PERI grants (20-FY02-56 and 21-FY07-605) and National Institutes of Health (NIH) grants (R21ES011666 and R01HD041702). The follow-up study is supported in part by grants from the Bunning family and their family foundations, Food Allergy Research & Education (FARE), and NIH grants (U01AI090727, R21AI079872, R21HD085556, R01HD041702, and R01HD086013). X.H. is supported by the NICHD (R03HD096136). We gratefully acknowledge the individuals who participated in the studies and contributed to this work. We also thank Ms Tami R. Bartell for her English-language editing. We also would like to acknowledge Linda Rosen and the Clinical Data Warehouse (CDW) for the assistance in obtaining relevant clinical information; CDW service is supported by the Boston University's Clinical and Translational Institute and NIH CTSA grant U54-TR001012. Funding Information: We gratefully acknowledge the individuals who participated in the studies and contributed to this work. We also thank Ms Tami R. Bartell for her English-language editing. We also would like to acknowledge Linda Rosen and the Clinical Data Warehouse (CDW) for the assistance in obtaining relevant clinical information; CDW service is supported by the Boston University's Clinical and Translational Institute and NIH CTSA grant U54-TR001012. Publisher Copyright: {\textcopyright} 2019 American Academy of Allergy, Asthma & Immunology",
year = "2019",
month = sep,
doi = "10.1016/j.jaci.2019.03.033",
language = "English (US)",
volume = "144",
pages = "729--737",
journal = "Journal of Allergy and Clinical Immunology",
issn = "0091-6749",
publisher = "Mosby Inc.",
number = "3",
}