MedPath

Soluble Corn Fiber Supplementation for Asthma

Phase 2
Completed
Conditions
Asthma in Children
Interventions
Drug: Soluble Corn Fiber
Registration Number
NCT03673618
Lead Sponsor
Phoenix Children's Hospital
Brief Summary

Studies of the importance of the human microbiome have demonstrated that microbial metabolites of fermentation of our dietary products (e.g. dietary fiber) have a multitude of health benefits. The investigators aim to determine whether supplementation of asthmatic children with soluble corn fiber alongside standard of care reduces airway inflammation driven by the gut microbial metabolites acetate, propionate, or butyrate (short chain fatty acids).

Detailed Description

Asthma is a complex inflammatory disease of the airways that is estimated to affect 300 million people worldwide. Incidence of asthma is steadily increasing in Western populations; an additional 100 million asthma diagnoses are anticipated by the year 2025. Asthma is a multifactorial disease affected by genetic and environmental factors. One major and potentially modifiable environmental factor is the Western diet. The Western diet influences the microbiome, which in turn, may influence inflammatory airway diseases via a gut microbiome-airway connection. The investigators hypothesize that prebiotic dietary fiber supplementation leads to increased circulating short chain fatty acid production and improvement in asthma disease activity. The investigators will recruit 20 children, ages 6-17 years old, with asthma from the Severe Asthma Clinic or General Pulmonary Clinic at Phoenix Children's Hospital. Participants will be randomly assigned (1:1) using a random number generator to ingest PROMOTIR soluble corn fiber (85% fiber, 12 g/day) in a fruit-flavored beverage or placebo (malodextrin in a similar fruit-flavored beverage) as previously described. Participants will be asked to consume the prebiotic soluble corn fiber (or placebo) for 4 weeks alongside their normal diet and normal asthma treatments. Blood will be collected pre- and post-fiber intervention to measure baseline and post-intervention circulating SCFAs. Stool samples and nasal wash will be collected for microbiome and immune analysis pre- and post- fiber consumption. Nasal washes will be collected pre- and post-fiber consumption to measure inflammatory patterns.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
20
Inclusion Criteria
  • Clinical diagnosis of asthma
  • Fractional excretion of exhaled nitric oxide (FeNO) > 50 ppb OR a history of environmental allergies
  • No emergency department or hospital visits for asthma in the past 3 months
  • No systemic corticosteroids in the past 1 month
  • Ability to consume a liquid drink of SCF or placebo
  • Ability to return for a 4-6 week follow-up visit
  • No special or unique diet as determined by PI/CO-Is.
Exclusion Criteria
  • Cystic fibrosis
  • Bronchiectasis
  • Change in asthma medicines other than short acting bronchodilators planned over the next 4-6 weeks.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
PROMOTIR soluble corn fiberSoluble Corn FiberParticipants will ingest PROMOTIR soluble corn fiber (85% fiber, 12 g/day) in a fruit-flavored beverage for 4 weeks alongside their normal diet and normal asthma treatments.
MalodextrinSoluble Corn FiberParticipants will ingest malodextrin in a fruit-flavored beverage for 4 weeks alongside their normal diet and normal asthma treatments.
Primary Outcome Measures
NameTimeMethod
Asthma symptoms4 weeks

Asthma Control Questionnaire

Secondary Outcome Measures
NameTimeMethod
Alpha and beta diversity in participants' nasal microbiomeBefore treatment period and after treatment for 4 weeks
Change in nasal wash Th2 gene expressionBefore treatment period and after treatment for 4 weeks
Alpha and beta diversity in participants' stool microbiomeBefore treatment period and after treatment for 4 weeks
Change in Serum Short Chain Fatty AcidsBefore treatment period and after treatment for 4 weeks

Trial Locations

Locations (1)

Phoenix Childrens Hospital

🇺🇸

Phoenix, Arizona, United States

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