Immunity
Conditions
Brief summary
With the rising prevalence of allergic diseases and the subsequent risk of developing other immune-related disorders, primary prevention of allergy has become a major priority. It is generally acknowledged that breastfeeding is one of the main pillars in allergy prevention. Infant formulas based on hydrolysed proteins have been developed to be used by infants at increased risk of developing allergy in case a mother is unable or chooses not to breastfeed her infant. It has recently been demonstrated that the gut microbiota composition and microbiota activity of infants receiving an infant formula based on partially hydrolysed proteins, supplemented with oligosaccharides, is more similar to breastfed infants than to infants receiving standard cow's milk formula, demonstrated by increased levels of bifidobacteria. However the interaction between microbial changes impacted by an hypoallergenic concept and its influence on early life immune development should be further explored. The aim of the present study is therefore to investigate the bifidogenic effect of a hypoallergenic formula supplemented with prebiotics and probiotics compared to standard infant formula in infants at increased risk of developing allergic disease. This study will secondary assess the effects of this concept on the development of allergic manifestations up to the age of 12 months, which will be verified in a separate clinical study MAESTRO as primary outcome. Furthermore, the effects on growth and safety will be studied.
Interventions
Intervention group: Infant Formula / Follow-On formula with partially hydrolysed cow's milk protein supplemented with prebiotics and probiotics.
Control group: Standard Infant Formula / Follow-On formula with intact cow's milk protein (only standard ingredients, without addition of pre- and probiotics).
Sponsors
Nutricia Research
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
No minimum to 16 Weeks
Healthy volunteers
Yes
Inclusion criteria
1. Healthy term infants (gestational age ≥ 37 and ≤ 42 weeks) at high risk of developing allergy based on family history of allergy (\*1). 2. Infants aged ≤ 16 weeks (max. 16 weeks + 0 days), preferably as soon as possible after birth. 3. Infants who start formula feeding within 16 weeks of age (infants of mothers who have chosen not to breastfeed or mothers who completely/partially cease breastfeeding before the subject's age of 16 weeks) (\*2) OR Infants who are exclusively breastfed and whose mothers have the intention to exclusively breastfeed at least until their infant is 16 weeks of age (\*2,3). 4. Written informed consent from one or both parents (according to local laws) and/or legal guardian. 1\* Family history of allergy is defined as at least one first-degree relative (parent or full sibling) with self-reported historically doctor confirmed allergic disease (allergic rhinitis, asthma, food allergy, allergic eczema). In case of a self-reported historically non-doctor confirmed allergic disease, doctor confirmation must be done as part of the screening procedure according to local practice (e.g. skin prick test, IgE measurement). 2\* Subjects whose mother intents to switch to formula feeding before the subject's age of 16 weeks but in the end still exclusively breastfeed, will be included in the breastfed reference group. The other way around, subjects whose mother intents to exclusively breastfeed for at least 16 weeks, but in the end decides to switch to formula earlier, will be included in the randomised groups. All these subjects should meet all other in-/
Exclusion criteria
. 3\* Exclusive breast feeding. WHO definition: only breast milk and no other liquids or solids except for drops or syrups consisting of vitamins, mineral supplements or medicines \[2\]. In addition to the WHO definition, in this study water is allowed as well as formula feeding during the first 72 hours of life. *
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Faecel levels of Bifidobacteria | 17 weeks | Levels of Bifidobacteria at 17 weeks of age - stool sample |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Faecal levels of Bifidobacteria and adult-like bacterial cluster | 52 weeks | Levels of Bifidobacteria and adult-like bacterial cluster up to 52 weeks of age - stool sample |
| IgE-mediated allergic manifestations | 52 weeks | IgE-mediated allergic manifestations up to 52 weeks of age - blood sample |
Countries
Belgium, Czechia, Germany, Hong Kong, Hungary, Israel, Italy, Netherlands, Singapore, Slovakia, Spain, Taiwan, United Kingdom
Outcome results
None listed