- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03495583
The EAT-On Study: Sensitisation, Allergy and Child Health
Effects of Early Introduction of Allergenic Foods Followed by Ad-libitum Consumption, on Food Allergic Sensitisation, Allergy and Measures of Child Health at 8 Years of Age in Exclusively Breastfed Infants
Study Overview
Status
Intervention / Treatment
Detailed Description
Sensitisation/Allergy:
Food allergy (FA) is common, increasing in prevalence and represents a public health concern in many countries. FA increasingly affects geographic regions where rates of FA were previously low.(1-5) Data from the Enquiring About Tolerance (EAT) study, which enrolled 1303 exclusively breastfed three month old babies from the general population, showed that 8% of children had proven immediate-onset FA at three years of age. This equates to almost 1 in 10 children. (1) The early-introduction of specific food allergen(s) to infant diets is a successful strategy for the prevention of FA. Introduction of peanut to the infant diet before 11 months of age, protected against the development of peanut allergy in a high-risk, atopic population.(6) This effect persisted despite cessation of peanut consumption for 12 months.(7) In the EAT Study, children from the general population were randomised either to consume six commonly allergenic foods (cow's milk, egg, peanut, wheat, fish and sesame) from four months of age (early introduction group (EIG)), or to follow Department of Health (DoH) advice to exclusively breastfeed until about 6 months of age (standard introduction group (SIG)). The per-protocol analysis revealed a reduction in any FA of 7.3% versus 2.4% (p=0.01), for peanut allergy of 2.5% versus 0% (p=0.003) and for egg allergy 5.5% versus 1.4% (p=0.009) in the SIG and EIG respectively. (8) In the EAT study, between 1 and 3 years an intention-to-treat analysis (ITT) of sensitisation to individual foods showed a significant cumulative treatment effect of 35% (p=0.0095) in the EIG (unpublished data). Furthermore, in the per-protocol analyses (PP), we showed a statistically significant reduction of 41.6% (p=0.01) in skin prick test (SPT) sensitivity to any food at 1 year, and again at 3 years with a 67.3% relative reduction (RR) (p=0.002) in the EIG. These findings were particularly significant for individual food; at 3 years there was a relative reduction in skin-prick sensitivity to all individual foods and particularly for peanut (RR 67.1% p=0.007).
FA is a dynamic condition with egg and milk allergy typically developing in infancy and being outgrown and peanut and sesame allergy usually developing between the ages of 3-6 and persisting into adulthood. Whilst early introduction of commonly allergenic foods is effective in preventing food allergy in early childhood and within the confines of a randomised controlled trial (RCT), the longevity of this novel approach has not been tested and little is known about whether these effects are sustained after 'real world' ad libitum consumption. The EAT-On Study aims to investigate this by following-up children who were previously enrolled in the EAT Study when they are 8 years of age and investigating the natural history of food allergy, and how the intervention that was applied when children were 4-6 months of age influences food allergic sensitisation and clinical food allergy when they are 8 years of age.
Child Health:
Whilst the UK Department of Health recommends exclusive breastfeeding (EBF) until around six months of age, surveys suggest this is achieved by only 1% of mothers(9). Given the lack of EBF till 6 months of age, the majority of infants will require additional nutrition provided from formula and/or solid weaning foods. Indeed, 75% of infants have been introduced to solid food by 5 months of age (9). The nutritional consequences of different weaning regimens may have important consequences on obesity outcomes, but rigorous trials in this area are difficult to undertake, not least because of the necessary ethical concerns that pertain to the comparison of breast-feeding with alternate or complementary feeding strategies. The EAT cohort presents a unique opportunity to study this question further as the diet consumed by children who participated in the EIG of the EAT study is much higher in protein than breastmilk alone. Good quality studies have found that consumption of high protein formula milk in early infancy increases the risk of overweight in later childhood compared with breastfeeding, but the effect of high protein solid food consumption alongside breastfeeding in early infancy has not been studied. The majority of infants have solid food introduced before 6 months of age, and updated guidance advocates the introduction of a high protein food (peanut) from 'around 6 months of age' (UK(10) and Australia(11)), or at 4 months of age (USA(12)) to prevent a new onset of peanut allergy. It is therefore timely to explore how early diet, particularly with respect to high protein weaning diet, influences childhood obesity. This will lead to the development of clearer guidance in respect to early weaning diet which extends to other high protein foods, while taking in to account the risk of childhood obesity.
The nature of the EAT cohort means that between 4 and 6 months of age children were randomised either to a lower protein diet (SIG) or to a higher protein diet (EIG): breastmilk contains approximately 6% energy from protein whilst the EIG were asked to consume a diet containing at least 15% energy from protein, more than double that of the SIG. This cohort therefore offers a unique opportunity to explore the effect of differing energy consumption from dietary protein on overweight/obesity and markers of cardiovascular health in later childhood.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
London, United Kingdom
- Paediatric Allergy
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Previous participation in the EAT study
- Age 8 years +/- 12 months
Exclusion Criteria:
- None
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Early introduction
Six commonly allergenic foods introduced (in a randomly assigned order) into the diets of exclusively breastfed infants from about 3 months of age.
|
Consumption of 2g/week of cow's milk, hen's egg, wheat, peanut, sesame and fish protein from 3 months of age (alongside breastfeeding)
|
No Intervention: Standard introduction
Infants followed UK DoH standard advice for weaning
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Allergic sensitisation
Time Frame: 3 years
|
Between group differences in total number of cumulative sensitisations to the six study food allergens at age 8
|
3 years
|
Food allergy
Time Frame: 3 years
|
Between group differences in cumulative food allergy (challenge confirmed) t the six study foods at age 8
|
3 years
|
Child Health
Time Frame: 3 years
|
Between group differences in proportion of children who classified as overweight or obese as determined by their BMI and/or BMI z score
|
3 years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Other allergic sensitisations
Time Frame: 3 years
|
Between group differences in proportion of children with SPT sensitisation to additional food allergens (hazelnut, brazil nut, cashew, almond and walnut) and aero-allergens (timothy grass, birch pollen, house dust mite, cat and dog dander).
|
3 years
|
Mechanisms of allergy
Time Frame: 3 years
|
Between group differences in specific IgE, IgG and IgG4 to peanut, egg, sesame and aeroallergens
|
3 years
|
Coeliac disease
Time Frame: 3 years
|
Between group differences in prevalence of coeliac disease using coeliac antibody test (tTG IgA) screening test
|
3 years
|
Atopic dermatitis
Time Frame: 3 years
|
Between group differences in prevalence of atopic dematitis
|
3 years
|
Allergic rhinoconjunctivitis
Time Frame: 3 years
|
Between group differences in prevalence of seasonal and perennial rhinoconjunctivitis
|
3 years
|
Asthma
Time Frame: 3 years
|
Between group differences in prevalence of asthma
|
3 years
|
Oral allergy syndrome
Time Frame: 3 years
|
Between group differences in prevalence of oral allergy syndrome
|
3 years
|
Parent reported food allergy
Time Frame: 3 years
|
Between group differences in food reaction history (parent-reported immediate onset food allergy)
|
3 years
|
Sibling allergies
Time Frame: 3 years
|
Prevalence of sibling allergies (food allergies, eczema, asthma and rhinitis)
|
3 years
|
AGE Level in association with food allergies
Time Frame: 3 years
|
Between group differences in AGE levels in association with food allergies
|
3 years
|
Skin fold thickness
Time Frame: 3 years
|
Between group differences in skin fold thickness (triceps and subscapular)
|
3 years
|
Circumference measurements
Time Frame: 3 years
|
Between group differences in midarm, waist and head circumference
|
3 years
|
Anthropometric ratios
Time Frame: 3 years
|
Between group differences in; adjusted weight for height; waist; height ratio; height adjusted weight circumference
|
3 years
|
Fat free mass
Time Frame: 3 years
|
Between group differences in fat free mass
|
3 years
|
Conicity index
Time Frame: 3 years
|
Between group differences in conicity index (calculated from waist circumference and height and weight measurements)
|
3 years
|
Cardiovascular health
Time Frame: 3 years
|
Between group differences in the proportion of children with cardiovascular measurements outside the expected range
|
3 years
|
Vascular stiffness
Time Frame: 3 years
|
Between group differences in vascular stiffness
|
3 years
|
AGE
Time Frame: 3 years
|
Between group differences in advanced glycation end products (AGE)
|
3 years
|
Inflammation
Time Frame: 3 years
|
Between group differences in inflammation (measured using IL=6; sensitive CRP; TNF alpha; MCP-1; RANTES chemokine
|
3 years
|
Metabolic and endocrine
Time Frame: 3 years
|
Between group differences in insulin, IGF-1 and leptin
|
3 years
|
White cell count
Time Frame: 3 years
|
Between group differences in total white blood cell count
|
3 years
|
Macronutrient dietary intake
Time Frame: 3 years
|
Between group differences in macronutrient intake
|
3 years
|
Dietary habits
Time Frame: 3 years
|
Between group differences in fussy eating
|
3 years
|
Physical activity
Time Frame: 3 years
|
Influence of physical activity on anthropometry and body composition measurements
|
3 years
|
Genetic influences
Time Frame: 3 years
|
Influence of parental size on: height; weight; waist circumference on participant's size
|
3 years
|
Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- GN2551
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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