Allergy Clinical Trial
— PROOM-3Official title:
Combined Dietary Supplementation With Lactobacillus Reuteri and Omega-3 PUFA During Pregnancy and Postnatally in Relation to Development of IgE-associated Disease During Infancy
The incidence of allergic disease has increased worldwide during the last decades.
Initially, a lot of effort has been put in elucidating which of the known risk factors
commonly associated to the development of allergic disease early in life was the cause of
this increase. Studies showing a reduced incidence of allergic disease in the former
socialist countries in comparison to countries with a "Western lifestyle" have shown that
risk factors as allergen exposure, environmental pollution and tobacco exposure are also
present in societies with a less affluent lifestyle. This suggests the disappearance of
factor protecting against the development of allergic diseases in affluent environment.The
development of allergic diseases begins during the first year of life with eczema, both
non-IgE- and IgE-associated, and food allergy, progressing during childhood with the
development of asthma bronchiale, also both non-IgE- and IgE-associated, and later
development of allergic rhinoconjunctivitis, i.e. the atopic march. The immune system of the
neonate is influenced by maternal immunity, both via the placenta and breast milk. Thus, the
immunological interaction between the mother and her offspring is close during pregnancy and
lactation. The association of cord blood IgE levels with maternal but not paternal atopic
heredity, may depend on a possibly stronger placental Th2 shift in atopic mothers. Thus,
factors influencing/protecting against the development of allergic disease early in life,
would be important already during pregnancy, birth and early postnatal life. Two major
hypotheses have been assessed during the last decade: Proper microbial stimulation,
including the establishment of the gut flora in infancy and the relationship between low
omega 3-polyunsaturated fatty acids in the western diet and the incidence of allergic
disease.
This is a double blind randomized study. Families with at least one parent/sibling with
clinical symptoms/history of allergic disease will be invited to participate in this study.
Pregnant mothers will be included in the study at the 20th week of gestation. They will be
randomized to 4 study groups, one will receive placebo capsules, the second will receive
omega-3 PUFA supplementation and placebo regarding L. reuteri, the third will receive L.
reuteri and placebo regarding omega-3 PUFA and the fourth group will receive both omega-3
PUFA and L. reuteri supplementation. Omega-3 supplementation will be given to mothers from
pregnancy and lactation while L. reuteri will be given to the mothers during pregnancy and
later to the children during the first year of life.The children will be clinically followed
by an allergy nurse regularly. Questionnaires regarding data on environment, siblings, pets,
breast feeding, smoking exposure, upper respiratory and other infections and clinical
symptoms of allergic disease will be filled regularly. Skin prick tests (SPTs) will be
performed in the children at 6 and 12 months with milk, egg, wheat, peanut and cat. At 24
months, timothy and birch allergen extracts will be added. A pediatrician will assess the
children at 24 months of life and whenever it is needed during the study period. Dietary
habits will be assessed during pregnancy (25th gestational week) and 6 months after child
birth. Blood samples in the children will be taken from cord blood and at 6, 12 and 24
months of life. Maternal blood samples will be taken at 20th weeks of gestation and at child
birth. Milk samples will be collected 1-4 days after partus and monthly during the first 4
months of lactation. Maternal gastrointestinal function will be addressed by validated diary
cards. Saliva from the children and fecal samples from mother and child will also be
collected according to the following protocol.
Status | Recruiting |
Enrollment | 496 |
Est. completion date | June 2017 |
Est. primary completion date | June 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years to 45 Years |
Eligibility |
Inclusion Criteria: - pregnant women expecting a child with at least one parent or a sibling with clinical symptoms/history of allergic disease - breastfeeding for at least 3 months is mandatory for inclusion in the statistical assessment in the study Exclusion Criteria: - mothers with fish allergy - twin pregnancy - mothers previously/currently using omega-3 PUFA or probiotic dietary supplementation - children born before gestational week 33 or seriously ill will be excluded from the study. |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention
Country | Name | City | State |
---|---|---|---|
Sweden | Allergicentrum, Universitetssjukhuset | Linköping |
Lead Sponsor | Collaborator |
---|---|
Ostergotland County Council, Sweden |
Sweden,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | IgE associated disease | A food reaction is defined as gastrointestinal symptoms, hives, aggravated eczema or wheezing following ingestion of a certain food with recovery after food elimination from the diet and reoccurrence of symptoms after ingestion of the particular food. Eczema is characterized as reoccurring, itching eczematous and lichenified or nummular dermatitis. Doctor diagnosed wheezing at least three times during the first two years is required for the diagnosis of asthma. If specific positive SPT or serum IgE antibodies is present, the food reaction, eczema in defined as IgE associated. | 2 years of age | No |
Secondary | Maternal gastrointestinal function | Maternal gastrointestinal function will be addressed by validated diary cards. The mothers will record every single stool, stool consistency, and corresponding defecatory symptoms (urgency, straining, and feeling of incomplete evacuation) for seven days at gestational week 25 and 35. Stool consistency will be defined by the Bristol Stool Form Scale. The mothers will also record every meal, and episodes (start and ending time) of abdominal pain and bloating. | 20th gestational week to 6 months post partum | No |
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