Early Introduction of Novel and Less-Studied Food Allergens in the Plant-Based Era: Considerations for US and EU Infant Formula Regulations
Abstract
:1. Introduction
- (1)
- Do fortified plant-based infant formulas, compliant with FDA regulations and EFSA (European) guidelines, support adequate infant growth?
- (2)
- Are plant-based infant formulas suitable for the management of cow’s milk allergy (CMA)?
- (3)
- Does feeding with novel plant-based infant formulas increase the risk of food allergies to the food allergens they contain?
- (4)
- Does feeding infants plant-based food allergens in early life increase the risk of allergic and severe allergic reactions?
2. Methods
3. Overview
3.1. Do Fortified Plant-Based Infant Formulas, Compliant with FDA Regulations and European Food Safety Authority (European) Guidelines, Support Adequate Infant Growth?
3.1.1. Rice Formula
3.1.2. Soy Formula
- Conclusion
- Recommendation
3.2. Are Plant-Based Infant Formulas Suitable for the Management of Cow’s Milk Allergy?
3.2.1. Rice-Based Formula
3.2.2. Soy-Based Formula
3.3. Does Feeding Novel Plant-Based Infant Formulas Increase the Risk of Food Allergies to the Food Allergens They Contain?
3.3.1. Prevalence of Almond Allergy
- -
- Sensitization
- -
- Self-reported rates
- -
- Self-reported clinician’s/doctor’s diagnosis (not based on oral food challenges)
- -
- Oral food challenges (OFCs).
- Conclusion
- Recommendation
3.3.2. Prevalence of Buckwheat Allergy
- -
- Self-reports
- Conclusion
- Recommendations
3.3.3. Early Introduction of Food Allergens
- Conclusion
- Recommendation
3.4. Does Feeding Infants Plant-Based Food Allergens in Early Life Increase the Risk of Allergic and Severe Allergic Reactions?
- Conclusion
- Recommendation
4. Overall Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
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Study | Number of Study Participants | Age of Participants | Study Duration | Classification of Infants Included in the Study | Number of Study Participants Receiving Rice Hydrolysate | Number of Study Participants Receiving Other Formulas | Number of Participants in Control Groups |
---|---|---|---|---|---|---|---|
Randomized [29] | 16 | 6–16 months | 6 months | CMA | 8 | 8 soy | |
Randomized [30] | 80 | 2 days | 4 months | Healthy | 32 | 33 cow’s milk | |
Randomized [31] | 160 | 5 months | 6 months | CMA | 30 | 31 extensively hydrolyzed 32 soy | 32 breastfed |
Non-randomized [32] | 88 | 29–25 months | 2 years | CMA | 15 | 26 extensively hydrolyzed 17 soy | 30 healthy |
No control [28] | 40 | <6 months | 6 months | CMA | 40 | NA |
Country | Age of Study Participants | Sensitization—SPT (% with a Positive SPT) | Sensitization—IgE (% with Positive Specific IgE Levels) | Self-Reported Reactions | Self-Reported Reactions Based on a Clinical Diagnosis | Sensitization (Positive SPT or Specific IgE Levels and Good Clinical History of Allergic Reaction) | Positive OFC |
---|---|---|---|---|---|---|---|
Hungary [48] | 20–69 years | NA | NA | NA | NA | NA | NA |
Hungary [48] | 60–97 years | NA | 0 (0–0.42) | NA | NA | NA | NA |
Iceland [49] | 18 months | NA | NA | 0 (0–1.5) | NA | 0 (0–1.5) | NA |
Sweden [49] | 18 months | NA | NA | 0 (0–1.4) | NA | 0 (0–1.4) | NA |
Sweden [55] | 4 years | NA | NA | 3.8 (3.1–4.7) | NA | NA | NA |
Turkey [50] | 6–9 years | 0 | NA | 0 | NA | NA | 0 |
United Kingdom [51] | 1 year | NA | NA | NA | NA | NA | 0 (0–0.5) n = 900 |
United Kingdom [56] | 2 years | NA | NA | NA | NA | NA | 0 (0–0.6) |
United Kingdom [56] | 3 years | 0.3 (0.0–1.2) | NA | NA | NA | NA | 0.2 (0.0–0.9) |
United Kingdom [57] | 7 years | 0.5 (0.2–0.9) | NA | NA | NA | NA | |
United States [52] | >18 years | NA | NA | NA | 0.9 (0.7–1.1) | NA | NA |
United States [58] | ≥18 years | NA | NA | NA | 1.6 (1.4–1.9) | NA | NA |
United States [53] | All children < 18 years | NA | NA | NA | 0.7 (0.6–0.8) | NA | NA |
United States [53] | Infants < 1 year | NA | NA | NA | 0.2 (0.1–0.5) | NA | NA |
Australia [54] | 6 years | NA | NA | NA | 0.3 (0.1–0.5) | NA | 0.3 (0.1–0.5) |
Country | Age of Study Participants | Sensitization—SPT (% with a Positive SPT) | Sensitization—IgE (% with Positive Specific IgE Levels) | Self-Reported Reactions | Self-Reported Reactions Based on a Clinical Diagnosis | Sensitization (Positive SPT or Specific IgE Levels and Good Clinical History of Allergic Reaction) | Positive OFC |
---|---|---|---|---|---|---|---|
Korea [60] | 12–15 years | NA | NA | 0.1 (0.1–0.2) | NA | NA | NA |
Korea [60] | 6–12 years | NA | NA | 0.1 (0.1–0.1) | NA | NA | NA |
Korea [61] | 6–16 years | NA | NA | 0.3 | NA | NA | NA |
Japan [62] | 5–10 years | NA | NA | 0.22 | NA | NA | NA |
China [63] | 13–21 years | NA | NA | 0.4 | NA | NA | NA |
Study Acronym | Full Study Title | Study Type | Population Included | Food Allergen Introduction Intervention | Primary Outcome | Results |
---|---|---|---|---|---|---|
LEAP (UK) [66] | Learning Early About Peanut Allergy | Non-blinded RCT (n = 640) | High-risk infants with moderate to severe eczema and/or egg allergy | Thrice-weekly consumption of 2 g of peanut protein vs. complete avoidance of peanut after randomization at 4–11 months, through 60 months of life | IgE-mediated peanut allergy based on OFC at month 60 | ITT analysis showed prevalence of peanut allergy of 13.7% in the avoidance group vs. 1.9% in the consumption group (p < 0.001) |
STAR (Australia) [67] | Solids Timing for Allergy Reduction | Blinded RPCT (n = 86) | High-risk infants with moderate to severe eczema | Daily consumption of 0.9 g raw whole egg powder (0.4 g protein/day) vs. placebo powder from 4 to 8 months of age Cooked egg consumption from 8 months onwards | IgE-mediated egg allergy at 12 months based on positive SPT and egg OFC | Study was terminated early as 1/3 of patients reacted to egg during entry OFC At 12 months, 33% had egg allergy in egg consumption group vs. 51% in control (not significant) |
PETIT (Japan) [68] | Preventing egg allergy in infants with AD | Blinded RCT (n = 121) | High-risk infants with atopic dermatitis | Daily consumption of 50 mg heated egg from 6 to 9 months Daily consumption of 250 mg heated egg from 9 to 12 months | IgE-mediated egg allergy at 12 months of age based on OFC | Prevalence of egg allergy was 37.7% in placebo vs. 8.3% in egg consumption group (p = 0.0013) No SAEs were reported |
STEP (Australia) [69] | Starting Time for Egg Protein | Blinded RPCT (n = 820) | Intermediate risk: atopic mothers (allergic disease + positive envir SPT Infants: no allergic diagnosis | Daily consumption of 0.9 g raw whole egg powder (0.4 g protein/day) vs. placebo powder from 4 to 6.5 months | IgE-mediated egg allergy at 12 months based on positive SPT and egg OFC | No significant differences in egg allergy between the groups No anaphylactic reactions were reported during initial egg introduction |
BEAT (Australia) [70] | Beating Egg Allergy Trial | Blinded RPCT (n = 319) | Intermediate risk: infants with 1st degree relative with atopy Infants: neg egg SPT | Daily consumption of 350 mg raw, whole egg protein vs. placebo powder from 4 months of age Cooked egg from 8 months of age | Sensitization to egg by SPT at 12 months of age | Subjects in egg consumption group had significantly less egg sensitization (10.7% vs. 20.5%, p = 0.03) than the placebo group No anaphylactic reactions were reported during initial egg introduction |
HEAP (Germany) [71] | Hens Egg Allergy Prevention | Blinded RPCT (n = 406) | Normal-risk general population Infants with IgE < 0.35 kU/L at enrollment | Thrice-weekly consumption of 2.5 g egg protein from 4 to 6 months of age until 12 months | Sensitization to egg based on egg IgE ≥ 0.35 kU/L at 12 months of age | No significant different in egg allergy between the egg consumption (2.1%) and the placebo (0.6%) groups High rate of anaphylaxis during egg introduction at entry experienced |
ABC Trial (Japan) [72] | Atopy Induced by Breastfeeding or Cow’s Milk Formula | Non-blinded RCT (n = 312) | Intermediate risk: infants with 1st degree relative with atopy | Subjects were randomized to 2 interventions: (1) Active group: breast milk (BF) and/or cow’s milk (CMF) in first 3 days of life (2) Placebo group: BF and/or amino acid (EF)-based formula in first 3 days | Primary outcome: Sensitization to cow’s milk at 24 months Secondary outcomes: IgE-mediated milk allergy at 24 months based on OFC | Sensitization and cow’s milk allergy lower in the BF/EF group vs. the BF plus CMF group (relative risk 0.52 [sensitization] and 0.2 [cow’s milk allergy]) |
SPADE (Japan) [73] | Strategy for Prevention of Milk Allergy by Daily Ingestion of Infant Formula in Early Infancy | Non-blinded RCT (n = 518) | Normal-risk general population | Subjects were randomized between 1 and 2 months of age to daily consumption of at least 10 mL of cow’s milk formula (CMF) or avoidance of CM (soy formula) Ongoing breastfeeding recommended until 6 months of age | IgE-mediated milk allergy at 6 months of age based on OFC | ITT analysis showed that 2/242 in the ingestion-group (0.8%) vs. 17/249 in the avoidance group (6.8%) had milk allergy (p < 0.001) No SAEs were reported during the screening OFC |
EAT (UK) [11] | Enquiring About Tolerance | Non-blinded RCT (n = 1303) | Normal risk: exclusively breastfed until allergenic foods introduced | The early introduction group (EIG) introduced 2 g of peanut, cooked egg, cow’s milk, sesame, whitefish, wheat protein twice weekly at 3 months The standard introduction group (SIG) followed UK guidance to start introduction of solid foods from 6 months of age | IgE-mediated food allergy to at least 1 of the 6 allergens at 1 or 3 years of age based on OFC | ITT analysis showed no difference in food allergy between EIG (5.6%) vs. SIG (6.1%) (p = 0.32) PP analysis showed significantly less prevalence of peanut allergy (p = 0.003) and egg allergy (p = 0.009) in EIG vs. SIG |
PreventADALL (Norway, Sweden) [74] | Preventing Atopic Dermatitis and ALLergies | Non-blindedRCT (n = 2397) | Normal-risk general population | Randomized to 4 intervention groups: (1) no intervention; (2) skin; (3) food; (4) combined skin and food. Food: introduction of peanut, cow’s milk, egg, and wheat from 3 months of age vs. no specific advice on food intro | IgE-mediated peanut, cow’s milk, egg, or wheat allergy at 36 months of age based of OFC | ITT analysis showed prevalence of food allergy reduced in food intervention group compared to no food intervention group: risk difference −1.6% [95% CI −2.7 to −0.5]; OR 0.4, [95% CI 0.2 to 0.8] Reduced risk of food allergy was seen with peanut but not with other 3 foods |
COMEET Israel [75] | Early, continuing exposure to cow’s milk formula and cow’s milk allergy | Allocated based on parental preference of feeding (n = 1992) | Normal-risk general population | Study subjects were allocated to either (1) exclusive breastfeeding (EBF) or (2) at least 1 feed with CMF (+/− breastfeeding) daily for the first 2 months of life | IgE-mediated cow’s milk allergy by 12 months of age CMA was defined as having at least 2 of 3 criteria: (1) positive OFC (2) sensitization to cow’s milk (3) clear history of immediate reactions | IgE-mediated CMA was 1.58% in the EBF group vs. 0 in “mixed feeding” group (p < 0.001) IgE-mediated CMA was 0.7% in the per-protocol EBF group vs. 3.27% in breastfed infants with irregular cow’s milk exposure in first 2 months |
Japan [7] | Early introduction of very small amounts of multiple foods to infants | Blinded RCT (n = 163) | High-risk infants with atopic dermatitis | Study subjects were randomized to either (1) mixed-food-allergen powder which contained egg, milk, wheat, soybean, buckwheat, and peanuts, or (2) placebo powder at 3–4 months. The mixed-allergen powder contained 2.5 mg, 7.5 mg, and 20 mg of each food allergen plus probiotics—infants increased doses every 2 weeks | IgE-mediated food allergies up to 18 months Food allergy was defined as - sensitized to the food plus - clear history of reactions and/or a positive OFC | Food allergy was significantly lower in the mixed-powder group by 18 months vs. the placebo group (7/83 vs. 19/80, p = 0.0066) |
US [76] | Early Introduction of Multi-Allergen Mixture for Prevention of Food Allergy: Pilot Study | Non-blinded RCT (n = 180) | General population | Infants were randomized to eat (1) single-food-allergen powder (milk, egg, or peanut at 300 mg protein per day: 2100 mg protein/food allergen/week) vs. (2) two-food-allergen powder (milk/egg, egg/peanut, milk/peanut at 300 mg per mix per day: 1050 mg protein/food allergen/week) vs. (3) a multiple-food-allergen mix of 10 different food allergens (milk/egg/peanut/cashew/almond/shrimp/walnut/wheat/salmon/hazelnut)ba at 3.1) low [300 mg per day: 21 (3 mg × 7) mg/food allergen/week], 3.2) medium [63 (9 mg × 7) mg/food allergen/week], or 3.3) high doses [210 (30 mg × 7) mg/food allergen/week]) vs. no early introduction at 4–6 months | IgE-mediated food allergy at 2 and 4 years using OFC | Study participants in all three mixes of the 10 food allergens, irrespective of the dose, were significantly more likely to consume 8 g food allergen protein than the other groups (q < 0.01) |
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Venter, C.; Shamir, R.; Fleischer, D.M. Early Introduction of Novel and Less-Studied Food Allergens in the Plant-Based Era: Considerations for US and EU Infant Formula Regulations. Nutrients 2023, 15, 4530. https://doi.org/10.3390/nu15214530
Venter C, Shamir R, Fleischer DM. Early Introduction of Novel and Less-Studied Food Allergens in the Plant-Based Era: Considerations for US and EU Infant Formula Regulations. Nutrients. 2023; 15(21):4530. https://doi.org/10.3390/nu15214530
Chicago/Turabian StyleVenter, Carina, Raanan Shamir, and David Mark Fleischer. 2023. "Early Introduction of Novel and Less-Studied Food Allergens in the Plant-Based Era: Considerations for US and EU Infant Formula Regulations" Nutrients 15, no. 21: 4530. https://doi.org/10.3390/nu15214530
APA StyleVenter, C., Shamir, R., & Fleischer, D. M. (2023). Early Introduction of Novel and Less-Studied Food Allergens in the Plant-Based Era: Considerations for US and EU Infant Formula Regulations. Nutrients, 15(21), 4530. https://doi.org/10.3390/nu15214530