Abstract

Rice products marketed in the USA, including baby rice cereal, contain inorganic arsenic, a putative immunotoxin. We sought to determine whether the timing of introduction of rice cereal in the first year of life influences occurrence of infections, respiratory symptoms, and allergy. Among 572 infants from the New Hampshire Birth Cohort Study, we used generalized estimating equation, adjusted for maternal smoking during pregnancy, marital status, education attainment, pre-pregnancy body mass index, maternal age at enrollment, infant birth weight, and breastfeeding history. Among 572 infants, each month earlier of introduction to rice cereal was associated with increased risks of subsequent upper respiratory tract infections (relative risk, RR = 1.04; 95% CI: 1.00–1.09); lower respiratory tract infections (RR = 1.19; 95% CI: 1.02–1.39); acute respiratory symptoms including wheeze, difficulty breathing, and cough (RR = 1.10; 95% CI: 1.00–1.22); fever requiring a prescription medicine (RR = 1.22; 95% CI: 1.02–1.45) and allergy diagnosed by a physician (RR = 1.20; 95% CI: 1.06–1.36). No clear associations were observed with gastrointestinal symptoms. Our findings suggest that introduction of rice cereal earlier may influence infants’ susceptibility to respiratory infections and allergy.

Highlights

  • Rice products marketed in the USA, including baby rice cereal, contain inorganic arsenic, a putative immunotoxin

  • In light of the vulnerability of infants to early life environmental exposures, we investigated the timing of introduction of rice cereal during their transition to solid food in first year of life and subsequent risk of infections, immune-related symptoms, and allergies as part of the New Hampshire Birth Cohort Study (NHBCS)

  • Of the 1760 pregnancies enrolled in the NHBCS as of October 2017, a total of 983 infants had complete follow-up data up to at least age of 8 months

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Summary

Introduction

Rice products marketed in the USA, including baby rice cereal, contain inorganic arsenic, a putative immunotoxin. Studies have reported associations between in utero arsenic exposure and a number of adverse outcomes including infant infections and respiratory outcomes among highly exposed populations in Bangladesh and among US i­nfants[20–22].

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