Food allergy (FA) impacts 8% of children in the United States (US),1 with disease prevalence varying by race and highest rates observed among Black children.2,3 However, it is unclear what factors may underlie racial differences in prevalence. Racial differences in timing of food allergen introduction during infancy may influence FA development and disease manifestation. The NIAID released the Addendum Guidelines for the Prevention of Peanut Allergy in the US in 2017 (PPA guidelines). The PPA guidelines encourage peanut allergy risk assessment for infants and introduction of peanut products into an infant’s diet around 4-6 months of age for those at high risk.4
In the Enquiring About Tolerance (EAT) study, non-White participants had higher rates of FA and were less likely to adhere to the early introduction feeding protocol.5 Racial differences in the timing of food allergen introduction among infants have yet to be extensively studied in the US. Therefore, this study aims to identify potential racial differences in parent/caregiver-reported timing of infant introduction to peanut, milk, and egg products among children with allergies to these foods.
Black and White children ≤12 years old with allergist-diagnosed IgE-mediated FA(s) were enrolled in the multi-site, Food Allergy Outcomes Related to White and African American Racial Differences (FORWARD) cohort, whose study design has been previously published.6 This study is a cross-sectional analysis of parent/caregiver-reported study baseline data at least 3 years after the participant’s first year of life. Sample sociodemographic characteristics are reported in Table 1 and compared across racial groups. Among children whose parent/caregiver reported feeding specific food allergens, chi-squared tests assessed associations by race concerning the age (≤ 6 months, 7-11 months, >11 months) at which children with specific FAs (i.e., peanut, egg, and/or milk -including cow’s milk formula) were first introduced to that specific food. Multiple logistic regression analyses presented in Table E1 assessed determinants of earlier or later allergen introduction, including adjustment for child age, race (Black vs White), eczema status (yes vs no), number of parent/caregiver-reported food allergies (multiple vs single), gender (female vs male), and study recruitment site.
Table 1:
All Participants N=632 |
Black Participants N=234 |
White Participants N=398 |
X2; P value | |
---|---|---|---|---|
Gender | ||||
Male | 242 (38.1%) | 79 (34.1%) | 163 (40.3%) | X2=2.2; P = .14 |
Female | 394 (61.9%) | 153 (65.9%) | 241 (59.7%) | |
Birth Year | ||||
Before 2008 | 81 (13.0%) | 39 (17%) | 42 (10.6%) | X2= 19.9; P < .001 |
2008-2017 | 423 (67.8%) | 164 (71.6%) | 259 (65.6%) | |
After 2017 | 120 (19.2%) | 26 (11.4%) | 94 (23.8%) | |
Child Age Mean(SD) | 6.0 (3.7) | 7.0 (3.6) | 5.4 (3.5) | T=5.5 P<.001 |
Site | ||||
Ann & Robert H. Lurie Children’s Hospital of Chicago | 212 (33.5%) | 68 (29.1%) | 144 (36.2%) | X2= 30.5; P < .0001 |
Rush University Medical Center | 128 (20.3%) | 73 (31.2%) | 55 (13.8%) | |
Children’s National Hospital | 138 (21.8%) | 51 (21.8%) | 87 (21.9%) | |
Cincinnati Children’s | 154 (24.4%) | 42 (17.9%) | 112 (28.1%) | |
Household Income | ||||
<$50,000 | 132 (21.4%) | 115 (52.3%) | 17 (4.3%) | X2= 232.6; P < .0001 |
$50,000 - $99,999 | 95 (15.4%) | 40 (18.2%) | 55 (13.9%) | |
$100,000-$149,999 | 96 (15.6%) | 23 (10.5%) | 73 (18.4%) | |
$150,000-$199,999 | 58 (9.4%) | 6 (2.7%) | 52 (13.1%) | |
$200,000-$299,999 | 90 (14.6%) | 10 (4.5%) | 80 (20.2%) | |
>$300,000 | 85 (13.8%) | 5 (2.3%) | 80 (20.2%) | |
Decline to Answer | 61 (9.9%) | 21 (9.5%) | 40 (10.1%) | |
Highest parental education attained by respondent | ||||
Some high school, no diploma | 9 (1.5%) | 8 (3.6%) | 1 (0.3%) | X2 = 182; P < .0001 |
High school or equivalent | 43 (7.0%) | 37 (16.8%) | 6 (1.5%) | |
Some college, no degree | 90 (14.6%) | 67 (30.5%) | 23 (5.8%) | |
Associate degree | 37 (6.0%) | 23 (10.5%) | 14 (3.5%) | |
Bachelor’s degree | 170 (27.6%) | 39 (17.7%) | 131 (33.0%) | |
Master’s degree | 181 (29.3%) | 35 (15.9%) | 146 (36.8%) | |
Professional degree | 25 (4.1%) | 3 (1.4%) | 22 (5.5%) | |
Doctoral degree | 62 (10.0%) | 8 (3.6%) | 54 (13.6%) | |
Type of FA | ||||
Peanut | 413 (65.3%) | 153 (65.4%) | 260 (65.3%) | X2 = 0; P >.99 |
Milk | 150 (23.7%) | 54 (23.1%) | 96 (24.1%) | X2 = 0.1; P =.84 |
Egg | 249 (39.4%) | 84 (35.8%) | 165 (41.5%) | X2 = 1.7; P =.19 |
Comorbid Conditions | ||||
Asthma | 236 (38.2%) | 128 (57.9%) | 108 (27.2%) | X2 = 57.0; P < .001 |
Eczema | 506 (81.9%) | 184 (83.6%) | 322 (80.9%) | X2 = 0.54; P = .46 |
Environmental Allergy | 289 (46.8%) | 136 (61.8%) | 153 (38.5%) | X2 = 29.9; P < .001 |
OAS | 51 (8.3%) | 22 (10.0%) | 29 (7.3%) | X2 = 1.0; P = .31 |
Some missingness (<5% of cases) was observed for demographic variables, which accounts for the differences between the Ns in row 1 and for specific variables (e.g. household income, educational attainment).
Overall, 632 children with FA (234 Black and 398 White; mean [SD] age=6.0[3.7]) were included in the analyses (Table 1). Peanut allergy was the most common food allergen among participants (65.3%) with similar prevalence by race (Black: 65.4% vs White: 65.3%, p>0.99). Reported peanut, milk, and egg introduction were delayed among Black children compared to their White counterparts. (Table 2).
Table 2.
Allergen Introduced | Age of Introduction | Black N (%) |
White N (%) |
X2; P Value |
---|---|---|---|---|
Peanut | Never introduced* | 45 (29.8%) | 92 (35.2%) | |
≤6 months | 8 (5.3%) | 36 (13.8%) | X2= 35.8; P < .001 | |
7-11 months | 9 (6.0%) | 50 (19.2%) | ||
>11 months | 89 (58.9%) | 83 (31.8%) | ||
Median(IQR) in months | 12.0 (12.0-24.0) | 10.0 (7.0-12.0) | P& < .001 | |
Milk | Never introduced* | 13 (23.6%) | 15 (15.8%) | |
≤6 months | 12 (21.8%) | 39 (41.1%) | X2 = 17.0; P ≤ .001 | |
7-11 months | 6 (10.9%) | 24 (25.3%) | ||
>11 months | 24 (43.6%) | 17 (17.9%) | ||
Median(IQR) in months | 12.0 (6.0-12.0) | 6.0 (2.0-10.0) | P& < .001 | |
Egg | Never introduced * | 36 (43.4%) | 48 (29.6%) | |
≤6 months | 3 (3.6%) | 29 (17.9%) | X2=16.9; P < .001 | |
7-11 months | 16 (19.3%) | 49 (30.2%) | ||
>11 months | 28 (33.7%) | 36 (22.2%) | ||
Median(IQR) in months | 12.0 (9.0-12.0) | 9.0 (7.0-12.0) | P& < .001 |
p value corresponds to Wilcoxon rank-sum test
Question text: “Never introduced this food (Child tested positive to this food on skin prick or RAST test ”)
IQR=Interquartile Range
Presented Median (IQR) ages of allergenic solid introduction are restricted to respondents reporting dietary introduction
After adjusting for participant demographics and FA characteristics, White children were more likely to have been introduced to peanut (Odds Ratio (OR) 2.6, 95% Confidence Interval (CI) 1.1-7.2) and milk (OR 2.7, CI 1.1-6.7) at ≤ 6 months, compared to Black children (Table E1). Delay of introduction (> 11 months of age) was less likely among White children for peanut (OR 0.1 3, CI 0.1-0.5), and milk (OR 0.2, CI 0.1-0.6) compared to Black children. Egg was not statistically significant for early or delayed introduction. As visualized in Figure E1, racial differences in timing of egg introduction adjusting by categorical birth year, participants born between 2017-2019 were more likely to have been introduced to peanuts at ≤ 6 months (OR 6.3, CI 1.5-44.4) and less likely to have delayed peanut introduction (OR 0.1, CI 0.01-0.2) compared to children born before 2008. There were no differences in early introduction of peanut, egg, and milk by gender among children born between 2008-2016 compared to children born before 2008.
This study is the first to explore racial differences in common food allergen feeding practices during infancy, where Black children were less likely introduced to peanut and cow’s milk during the first year of life compared to White children. The observed differences in infant introduction timing of peanut, milk, and egg in this study may relate to the growing burden of and increased prevalence of FAs among Black children.1,3,7,8 Nearly 89% of Black children with peanut allergy were not introduced to peanuts by 1 year of age or never introduced to peanuts compared to 67% of White children with peanut allergy. It is unclear if decisions to withhold or delay peanut feeding were due to varying pediatric clinician recommendations, identification, and management of high risk for FAs, parental fears of introducing allergens, cultural practices among respondents, and/or high allergic sensitization to peanut. It is possible that differences in knowledge regarding the safety and effectiveness of early allergen introduction for prevention varies among parents/caregivers. Previous literature suggests that while caregiver knowledge about pediatric FAs is generally suboptimal, misperceptions were more frequently reported among racial/ethnic minority respondents and those reporting lower household income.9
This study has several limitations. Although FORWARD is a prospective cohort study, these data were collected at study baseline, at least 3 years after the child’s birth. Additionally, a greater proportion of Black children were born before 2008, a smaller proportion of Black children were born between 2017-2019 and the mean age of Black children was 1.6 years older than White children in the study. Therefore, recall bias is possible and may be differential by race, despite adjustment for child age in the regression models. Selection bias is also possible, however the survey completion rate among eligible respondents in the study was >95% and low rates of missingness were observed (<3% for all variables). Furthermore, the case definitions applied for peanut, milk, and egg allergy relied fully on parent/caregiver-report, which may result in false positive cases.
Our study underscores the need to better characterize racial and cultural differences by examining if barriers and facilitators exist to “early” introduction of food allergens to infants, which may inform culturally specific strategies to educate families on the benefits of early introduction of common food allergens. It is necessary to explore how physician recommendations for early introduction of food allergens influence parents’ decision to introduce foods, and the method of food introduction. Finally, the fact that many caregivers in this cohort of FA patients nevertheless reported introducing allergenic proteins “early,” suggests that further work is needed to better characterize the dietary exposures of diverse samples of allergic and non-allergic patients. Such work has the potential to inform ongoing intervention studies to determine the ideal timing of allergenic protein introduction during early childhood and support targeted interventions to reduce FAs in diverse pediatric populations, as well as optimize dosing, frequency, preparation, and dietary patterns for FA prevention.
Supplementary Material
Clinical Implications:
Exploring racial differences in parent/caregiver-reported timing of peanut, milk, and egg introduction may help better characterize factors influencing racial differences in the prevalence of food allergy (FA) and inform interventions to prevent FA among diverse populations.
ACKNOWLEDGEMENTS
This study was funded by the NIH (R01AI130384). We would like to thank additional FORWARD team members for their work contributing to the study design/enrolling participants. Team members include: Ann & Robert H. Lurie Children’s Hospital of Chicago: Lucy Bilaver, Johnathan Choi, Ososese Enaholo, Jamie Fierstein, Isabel Galic, Gwen Holtzman, Haley Hultquist, Khalid Ibrahim, Ashwin Kulkarni, Pamela Newmark, Sai Nimmagada, Jacqueline Pongracic, Eileen Vincent, Mark Wlodarski; Rush University Medical Center: Aame B Andy-Nweye, Susan Fox, Mahboobeh Mahdavinia; Cincinnati Children’s Hospital Medical Center: Annika Chura; Children’s National Hospital: Amaziah Coleman, Izeris Ortiz-Rodriguez.
Funding:
This study was funded by the NIH (R01 AI130384).
Conflicts of Interest:
Dr. Christopher Warren has served as an epidemiological consultant for Alladapt Immunotherapeutics
Dr. Hemant Sharma receives research grant support from Aimmune Therapeutics, DBV Technologies, Regeneron, Food Allergy Research & Education (FARE), and the National Institutes of Health (NIH).
Dr. Tobin receives research grant support from The National Institutes of Health (NIH) and Stanford Sean N. Parker Center for Allergy Research.
Dr. Assa’ad receives grant support from Aimmune Therapeutics, DBV Technologies, Sanofi Aventis, Astellas, AstraZeneca, Regeneron, and NIH.
Dr. Gupta receives research grant support from The National Institutes of Health (NIH), Food Research & Education (FARE), Stanford Sean N. Parker Center for Allergy Research, UnitedHealth Group, Thermo Fisher Scientific, Genentech, and the National Confectioners Association (NCA); and has served as a medical consultant/advisor for Aimmune Therapeutics, Genentech, Before Brands, Kaléo, DBV Technologies, ICER, DOTS Technology, and Food Allergy Research and Education (FARE).
The other authors do not have any conflicts of interest to disclose.
Footnotes
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