Use of a Probiotic Supplement to Prevent Asthma in Infants
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Purpose
The goal of the study is to understand the mechanisms of how antigen presentation affects the developing immune system and subsequently affects susceptibility to, or protects against, asthma development. This randomized controlled study will test the effectiveness of daily supplementation of Lactobacillus GG for the first 6 months of life on the early immunological development of asthma.
| Condition | Intervention |
|---|---|
|
Asthma |
Dietary Supplement: Probiotic Dietary Supplement: Placebo |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor) Primary Purpose: Prevention |
| Official Title: | Trial of Infant Probiotic Supplementation to Prevent Asthma |
- Development of atopic dermatitis [ Time Frame: Measured from birth to 3 years of age ] [ Designated as safety issue: No ]
- Early clinical markers of asthma, including frequent wheezing, wheezing without upper or lower respiratory tract infections, allergic rhinitis, atopic dermatitis, serum IgE, and eosinophilia [ Time Frame: Measured from birth to 3 years of age ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 276 |
| Study Start Date: | June 2005 |
| Estimated Study Completion Date: | January 2013 |
| Estimated Primary Completion Date: | January 2013 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Active Comparator: 1
Participants in this arm will receive Lactobacillus GG.
|
Dietary Supplement: Probiotic
Daily dose of ten to the tenth colony-forming units of Lactobacillus GG and 225 mg of inulin for the first 6 months of life.
Other Name: Culturelle
|
|
Placebo Comparator: 2
Participants in this arm will receive a placebo.
|
Dietary Supplement: Placebo
Daily dose of placebo supplement containing 325mg inulin for the first 6 month of life.
|
Detailed Description:
BACKGROUND:
During infancy, environmental factors may affect immune system development and lead to the development of asthma. The hygiene hypothesis suggests that the absence of endotoxin exposure leads to an unfavorable Th1/Th2 balance. Thus, a controlled antigen exposure during infancy may establish a Th1/Th2 balance that blocks the onset of asthma or slows the progression of the disease.
Lactobacillus is a bacterium commonly found in many foods (e.g., yogurt) in the typical childhood diet. It is also used as a probiotic supplement to prevent the development of diarrhea. Due to its safety and availability, Lactobacillus is an ideal bacterium to use as an antigen exposure to test the hygiene hypothesis.
Consistent with the hygiene hypothesis, observational studies suggest that early Lactobacillus exposure leads to decreased risk of developing atopic dermatitis, which has been associated with asthma in later years. The investigators are aware of no study that has examined the effect of Lactobacillus on the development of early markers of asthma in children at risk for developing the disease. They hypothesize that Lactobacillus can be used as an antigen exposure to establish a Th1/Th2 balance that blocks the development of early markers of asthma.
DESIGN NARRATIVE:
The hygiene hypothesis suggests that the absence of endotoxin exposure leads to an unfavorable Th1/Th2 balance. A controlled antigen exposure during infancy may help establish a Th1/ Th2 balance that blocks the onset or progression of asthma. Lactobacillus is a bacterium found in many foods in the typical pediatric diet, and is used as a supplement to prevent diarrhea. Due to the safety, feasibility, and early promising results in preventing atopic dermatitis, Lactobacillus is an ideal bacterium to use as an exposure to test the hygiene hypothesis. The investigators hypothesize that such an exposure may block or delay development of early markers of asthma.
The study will use a randomized placebo-controlled trial design to measure the effect of a 6-month daily exposure of Lactobacillus, as an infant supplement, on immune system and asthma development during the first 3 years of life.
The study will measure the effect of the antigen exposure on the presence and time to presentation of: (1) early clinical markers for asthma development (frequent wheezing, wheezing without colds, rhinitis, and atopic dermatitis); (2) early immunologic markers for asthma development (eosinophilia, immunoglobulin E); and (3) development of a T-helper phenotype (Th-1 vs Th-2). Investigators will characterize the Th phenotype by measuring the whole blood lymphocyte response to stimulants, focusing on Th1 (IFN-gamma, interleukin (IL)-12) and Th2 cytokines (IL-10, IL-4, IL-13), as well as real-time reverse transcriptase polymerase chain reaction (RT-PCR) with PCR amplification (TaqMan) to quantify RNA transcripts. Clinical and immunologic markers will be measured up to 3 years of age.
Adherence will be assessed using diaries, pill count, and Lactobacillus stool cultures.
The study will use intention-to-treat analysis and will control for the impact of family, environmental, diet, and demographic factors on outcomes using multivariate regression and survival analysis techniques. Investigators expect that when compared to controls, subjects receiving Lactobacillus will have decreased and delayed development of markers for asthma, and a greater likelihood of developing a Th1 phenotype.
Eligibility| Ages Eligible for Study: | up to 4 Days |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Inclusion criteria:
- Expectant parents either of whom have a history of asthma
- Parents willing to add a probiotic supplement or placebo to one feeding each day for 6 months
Exclusion criteria:
- A sibling currently or previously enrolled in the study
- Any major congenital birth deformities, acute illness at enrollment, or chronic conditions affecting food intake or metabolism
- Participation in another clinical study
- Infants from multiple gestation births (since only one child per family will be included in the study, incorporating a child from a multiple birth would add unnecessary burden to parents by requiring them to administer different formulas to different children)
Contacts and Locations| Contact: Michael D. Cabana, MD, MPH | 415-476-5473 | Michael.Cabana@ucsf.edu |
| Contact: Michelle L. McKean, MPH, RD | 415-476-2860 | McKeanm@peds.ucsf.edu |
| United States, California | |
| University of California, San Francisco | Recruiting |
| San Francisco, California, United States, 94118 | |
| Contact: Michael D. Cabana, MD, MPH 415-476-5473 Michael.Cabana@UCSF.EDU | |
| Contact: Michelle L. McKean, MPH, RD 415-476-2860 McKeanM@peds.ucsf.edu | |
| Principal Investigator: Michael D. Cabana, MD, MPH | |
| Principal Investigator: | Michael D. Cabana, MD, MPH | University of California, San Francisco |
More Information
Additional Information:
Publications:
| Responsible Party: | University of California, San Francisco |
| ClinicalTrials.gov Identifier: | NCT00113659 History of Changes |
| Other Study ID Numbers: | 187, R01HL080074, R01 HL080074 |
| Study First Received: | June 9, 2005 |
| Last Updated: | March 19, 2012 |
| Health Authority: | United States: Federal Government |
Keywords provided by University of California, San Francisco:
|
Asthma Probiotics Prevention Eczema |
Additional relevant MeSH terms:
|
Asthma Bronchial Diseases Respiratory Tract Diseases Lung Diseases, Obstructive Lung Diseases |
Respiratory Hypersensitivity Hypersensitivity, Immediate Hypersensitivity Immune System Diseases |
ClinicalTrials.gov processed this record on May 16, 2013