| Literature DB >> 35807839 |
Laurien Ulfman1, Angela Tsuang2, Aline B Sprikkelman3,4, Anne Goh5, R J Joost van Neerven1,6.
Abstract
Food allergy incidence has increased worldwide over the last 20 years. For prevention of food allergy, current guidelines do not recommend delaying the introduction of allergenic foods. Several groundbreaking studies, such as the Learning Early About Peanut Allergy study, showed that the relatively early introduction of this allergenic food between 4-6 months of age reduces the risk of peanut allergy. However, less is known about the introduction of cow's milk, as many children already receive cow's-milk-based formula much earlier in life. This can be regular cow's milk formula with intact milk proteins or hydrolyzed formulas. Several recent studies have investigated the effects of early introduction of cow's-milk-based formulas with intact milk proteins on the development of cow's milk allergy while breastfeeding. These studies suggest that depending on the time of introduction and the duration of administration of cow's milk, the risk of cow's milk allergy can be reduced (early introduction) or increased (very early introduction followed by discontinuation). The aim of this narrative review is to summarize these studies and to discuss the impact of early introduction of intact cow's milk protein-as well as hydrolyzed milk protein formulas-and the development of tolerance versus allergy towards cow's milk proteins.Entities:
Keywords: cow’s milk allergy (CMA); early introduction; food allergy; milk protein; prevention
Mesh:
Substances:
Year: 2022 PMID: 35807839 PMCID: PMC9268691 DOI: 10.3390/nu14132659
Source DB: PubMed Journal: Nutrients ISSN: 2072-6643 Impact factor: 6.706
Studies on very early introduction of cow’s milk in first days of life [45,46,47,48,49] and early introduction of cow’s milk [50,51,52,53,54,55,56,57].
| Study | Design | Population | Infants/ | Age Onset Introduction CM | CM Formula | Breastfeeding | CMA Diagnosis | Outcome |
|---|---|---|---|---|---|---|---|---|
| Kelly et al. [ | Retro- and prospective | Infants at risk | 55 infants | Within 24 h after birth | Regular CMF | BF only vs. BF + CMF | Allergy-focused clinical history, SPT, SpIgE measurement, and open food challenge, if necessary | Increased risk when CMF supplementation in first 24 h (OR 7.01; 95CI 1.79 27.01, |
| Host et al. [ | Prospective | General population | 1749 infants | Within first 3 days after birth | Regular CMF | BF population +/− early introduction of CMF in nursery | IgE and non-IgE, elimination/challenge test | 39/1539 infants that received supplementation with CMF in the first 3 days had confirmed CMA while none of 210 exclusively BF neonates developed CMA (0/210), |
| Gil et al [ | Retrospective | CMA + infants | 211 infants/group | Diverse | Regular CMF | Study focused on duration of IgE | IgE + CMA cases by clinical examination, provocation tests, serology | Increased risk when CMF supplementation in hospital, BF duration < 1 mo and 4–6 mo associated with higher risk of CMA while no increased risk of BF duration of 1–3 mo |
| Saarinen [ | Prospective | General population | 6209 infants | Within first 20 h of life, and average feeding time of 2 days after birth | Pasteurized breastmilk Regular CMF Ext.Hydrolyzed whey formula | BF population (exclusively or supplemented with CMF, Hydrolyzed or pasteurized breastmilk) | Interview, elimination/challenge test, SPT | Feeding of CM at maternity hospitals increases the risk of CMA when compared with feeding of other supplements, but exclusive breast-feeding does not eliminate the risk |
| Sakihara [ | Data from SPADE study. Randomized controlled trial | Participants who ingested CMF in the first 3 days of life | 431 children | 4 groups of breastfed infants who discontinued CMF ingestion | Mixed feeding groups (breastfeeding and cow’s milk formula (CMF) who discontinued CMF at different ages) | Breastfeeding + CMF in first 3 days of life +/− continuous CMF supplementation | Oral food challenge was performed to assess CMA development |
CMA incidence was significantly higher in the DISC < 1 month group ( |
| Tezuka [ | Prospective | General population | >80,000 children | CMF consumption was categorized in < 3 mo, 3–6 mo or 6–12 mo at introduction | Regular CMF | BF and mixed fed. | CMA was defined as an allergic reaction to a CM product in an individual not consuming CM products at the time of evaluation, combined with physician-diagnosed food allergy | Introducing regular consumption of formula within the first 3 months of age was associated with lower risk of CMA at 12 months. Regular consumption at 3–6 months was strongly associated with a reduction in 12-month CMA (adjusted relative risks [95% confidence intervals]: 0.22 [0.12–0.35]), whereas no association was observed at 0–3 months (1.07 [0.90–1.27] |
| Peters [ | Longitudinal | General population | 5276 | Exposed to CMF 0–3 months or not | Regular CMF | Excl BF, mixed feeding, excl FF | Parental report of a reaction to cow’s milk consistent with IgE-mediated symptoms and a positive cow’s milk skin prick test | Early exposure to cow’s milk protein was associated with a reduced risk of cow’s milk sensitization (adjusted odds ratio [aOR] 0.44, 95% confidence interval [CI] 0.23–0.83), parent-reported reactions to cow’s milk (aOR 0.44, 95% CI 0.29–0.67), and cow’s milk allergy (aOR 0.31, 95% CI 0.10–0.91) at age 12 months |
| Katz [ | Prospective | General population | 13019 | Age at CMF exposure | Regular CMF | Excl BF, mixed feeding, excl FF feeding | Interview followed by SPT and open food challenge | The mean age of cow’s milk protein (CMP) introduction was significantly different ( |
| Sakihara [ | Prospective | Hen’s-egg-allergic patients | 397, | Excl BF group , discont ingestion of CMF before 3 mo of age (temp group; continuous ingestion of CMF, but not daily, up to 3 months of age (nondaily group); continuous ingestion of CMF at least once daily (daily group) | Regular CMF | Excl BF and mixed feeding groups | (1) a positive OFC result or any convincing episode of immediate reaction within 2 h after the ingestion of a cow’s milk product and [ | The incidence of developing CMA between the breast-fed group and temporary group did not show any statistical difference. Nondaily group and daily group had significantly lower incidence of developing CMA in comparison to the breast-fed group (nondaily group odds ratio 0.43; |
| Lowe [ | Single-blind (participant) randomized controlled trial | Children with a family history of allergic disease | 620, 0–2 y old children. Follow up at 6–7 years | randomized to receive the allocated formula at cessation of breast-feeding | cow’s milk formula, a pHWF, or a soy formula | breast-feeding until cessation, followed by formula (cow’s milk formula, a pHWF, or a soy formula) | Skin prick tests to 6 common allergens (milk, egg, peanut, dust mite, rye grass, and cat dander) were performed at 6, 12, and 24 months. | The primary outcome was any allergic manifestation (cumulative incidence) |
| Perkin [ | Randomized controlled study | Exclusively breast-fed infants who were 3 months of age | 1303 exclusively breast-fed infants randomized to early introduction group of six allergenic foods standard introduction group | As of 3 months of age for early introduction and as of 6 months for standard introduction group | peanut, cooked egg, cow’s milk, sesame, whitefish, and wheat | In the standard-introduction group, there was no consumption of peanut, egg, sesame, fish, or wheat before 5 months of age and consumption of less than 300 mL per day of formula milk between 3 and 6 months of age | Double blind placebo controlled food challenges, skin prick testing |
The primary outcome was challenge-proven food allergy to one or more of the six early-introduction foods between 1 year and 3 years of age. In the intention-to-treat analysis, no significant differences were found. In the per-protocol analysis, the prevalence of any food allergy was significantly lower in the early-introduction group than in the standard introduction group (2.4% vs. 7.3%, |
| Sakihara [ | Randomized controlled trial (SPADE study) | Breastfed infants who | 491 participants (242 in the ingestion group and 249 in the avoidance group) | Start CMF between 1 and 2 months of age | ingest at least 10 mL of CMF daily (ingestion group) | Breastfeeding +/− CMF or soy formula | Oral food challenge was performed to assess CMA development, skin prick test, serum titers specific IgE and IgG4 | Primary outcome was CMA by oral food challenge. Secondary outcomes were proportion of infants with positive SPT and seruvm titers of specific IgE and IgG4. |
| Onizawa [ | Retrospectively | CMA-allergic patients and non-allergic controls | 51 IgE-CMA, 102 controls, 32 unmatched patients IgE egg. Over 1 year of age | Supplemented with CMF maternity clinic, excl BF, early regular CMF, delayed CMF, no early regular continuous CMF | Regular CMF | BF and mixed feeding population | Immediate allergic reactions, CM specific IgE (≥0.7 kUA/L), doctors diagnose of allergy | In a multivariable logistic regression analysis, the adjusted odds ratio of delayed (started more than 1 month after birth) or no regular cow’s milk formula (less than once daily) was 23.74 (95% CI, 5.39–104.52) comparing the CMA group with the Control group |