Single low‐dose exposure to cow’s milk at diagnosis accelerates cow’s milk allergic infants’ progress on a milk ladder programme

Background Cow's milk protein allergy (CMPA) is one of the most common food allergies in infancy. Most infants with CMPA tolerate baked milk from diagnosis and gradually acquire increased tolerance. Nevertheless, parents often display significant anxiety about this condition and a corresponding...

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Published inAllergy (Copenhagen) Vol. 77; no. 9; pp. 2760 - 2769
Main Authors d’Art, Yvonne M., Forristal, Lisa, Byrne, Aideen M., Fitzsimons, John, van Ree, Ronald, DunnGalvin, Audrey, Hourihane, Jonathan O'Brien
Format Journal Article
LanguageEnglish
Published Denmark Blackwell Publishing Ltd 01.09.2022
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Summary:Background Cow's milk protein allergy (CMPA) is one of the most common food allergies in infancy. Most infants with CMPA tolerate baked milk from diagnosis and gradually acquire increased tolerance. Nevertheless, parents often display significant anxiety about this condition and a corresponding reluctance to progress with home introduction of dairy due to concerns about possible allergic reactions. Objective To evaluate the impact on gradual home introduction of foods containing cows’ milk after a supervised, single low‐dose exposure to whole milk at time of diagnosis. Methods Infants less than 12 months old referred with suspected IgE‐mediated cow's milk allergy were recruited to an open‐label randomized, controlled trial of intervention—a single dose of fresh cow's milk, using the validated dose of milk that would elicit reactions in 5% of CMPA subjects—the ED05 – vs routine care. Both groups implemented graded exposure to CM (using the 12 step MAP Milk Tolerance Induction Ladder), at home. Parents completed food allergy quality of life questionnaires and State and Trait Anxiety Inventories (STAI). Main outcome measures were milk ladder position at 6 months and 12 months post‐randomization. Results Sixty patients were recruited, 57 (95%) were followed to 6 months. By 6 months, 27/37 (73%) intervention subjects had reached step 6 or above on the milk ladder compared to 10/20 (50%) control subjects (p = .048). By 6 months, 11/37 (30%) intervention subjects had reached step 12 (i.e. drinking unheated cow's milk) compared to 2/20 (10%) of the controls (p = .049). Twelve months post‐randomization, 31/36(86%) of the intervention group and 15/19(79%) of the control group were on step 6 or above. However, 24/37 (65%) of the intervention group were at step 12 compared to 7/20 (35%) of the control group (p = .03). Maternal STAIs were significantly associated with their infants’ progress on the milk ladder and with changes in skin prick test and spIgE levels at 6 and 12 months. Conclusion This study demonstrates the safety and effectiveness of introduction of baked milk implemented immediately after diagnosis of cows’ milk allergy in a very young cohort. A supervised single dose of milk at the ED05 significantly accelerates this further, probably by giving parents the confidence to proceed. Maternal anxiety generally reflects infants’ progress towards completion of the milk ladder, but pre‐existing high levels of maternal anxiety are associated with poorer progress. This study evaluates the impact on gradual home introduction of foods containing cow's milk after a supervised, single low‐dose exposure to whole milk at time of diagnosis. Step 6 or above on the milk ladder was reached by 73% intervention subjects and 50% control subjects. Step 12 was reached by 6 month by 30% intervention subjects and 10% of the controls. Babies of mothers with higher levels of maternal anxiety at baseline made poorer progress on the milk ladder during the 12‐month study period. ED05, eliciting dose for 5% of subjects tested; FAQL, food allergy related quality of life; MAP, milk allergy in primary care guideline; SPT, skin prick test.Abbreviations: ED05, eliciting dose for 5% of subjects tested; FAQL, food allergy‐related quality of life; MAP, milk allergy in primary care guideline; SPT, skin prick test
Bibliography:Funding information
YD was in receipt of a Clinical Research Fellowship from the National Children's Research Centre Ireland.
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ISSN:0105-4538
1398-9995
1398-9995
DOI:10.1111/all.15312