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Use of a Probiotic Supplement to Prevent Asthma in Infants

This study is currently recruiting participants.
Verified by National Heart, Lung, and Blood Institute (NHLBI), August 2008

Sponsored by: National Heart, Lung, and Blood Institute (NHLBI)
Information provided by: National Heart, Lung, and Blood Institute (NHLBI)
ClinicalTrials.gov Identifier: NCT00113659
  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 Supplement
Dietary Supplement: Placebo Supplement

MedlinePlus related topics:   Asthma    Dietary Supplements   

ChemIDplus related topics:   Inulin   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Prevention, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Placebo Control, Parallel Assignment
Official Title:   Trial of Infant Probiotic Supplementation to Prevent Asthma

Further study details as provided by National Heart, Lung, and Blood Institute (NHLBI):

Primary Outcome Measures:
  • Development of atopic dermatitis [ Time Frame: Measured from birth to 3 years of age ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • 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 2010
Estimated Primary Completion Date:   January 2010 (Final data collection date for primary outcome measure)

Arms Assigned Interventions
1: Active Comparator
Participants in this arm will receive a Lactobacillus GG supplement.
Dietary Supplement: Probiotic Supplement
Daily dose of 10 to the tenth colony-forming units of Lactobacillus GG and 225 mg of inulin for the first 6 months of life.
2: Placebo Comparator
Participants in this arm will receive a placebo.
Dietary Supplement: Placebo Supplement
Participants will receive a placebo supplement containing 325mg inulin.

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

Criteria

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

Please refer to this study by its ClinicalTrials.gov identifier: NCT00113659

Contacts
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    

Locations
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            

Sponsors and Collaborators

Investigators
Principal Investigator:     Michael D. Cabana, MD, MPH     University of California, San Francisco    
  More Information


Click here for the TIPS Asthma Research Project web site  This link exits the ClinicalTrials.gov site
 

Publications:

Responsible Party:   University of California, San Francisco ( Michael D. Cabana, MD, MPH )
Study ID Numbers:   187, R01 HL080074
First Received:   June 9, 2005
Last Updated:   August 20, 2008
ClinicalTrials.gov Identifier:   NCT00113659
Health Authority:   United States: Federal Government

Keywords provided by National Heart, Lung, and Blood Institute (NHLBI):
Asthma  
Probiotics  
Prevention  
Eczema  

Study placed in the following topic categories:
Hypersensitivity
Lung Diseases, Obstructive
Respiratory Tract Diseases
Lung Diseases
Hypersensitivity, Immediate
Asthma
Eczema
Respiratory Hypersensitivity

Additional relevant MeSH terms:
Immune System Diseases
Bronchial Diseases

ClinicalTrials.gov processed this record on October 03, 2008




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