How Reflux Medications Affect the Microbiome of Infants

Sponsor
Nemours Children's Clinic (Other)
Overall Status
Completed
CT.gov ID
NCT03747991
Collaborator
(none)
12
1
11.6
1

Study Details

Study Description

Brief Summary

The changes in the organisms making up the gut microbiota in infants who are taking anti-acid reflux medications (histamine 2 receptor antagonists) as compared to infants who are not taking these medications is not well-studied or understood. Whether these medications change the gut microbiota and microbiome, and what that change may imply for children on these medications, is the focus of this study.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Gut microbiota dysbiosis is associated with diseases ranging from localized gastrointestinal disorders to neurologic, respiratory, metabolic, hepatic, and cardiovascular illnesses. The microbial colonization of the infant gut is known to play a key role in immunologic and metabolic pathways impacting on human health. Disruptions during the complex process of microbial colonization have been shown to increase disease susceptibility during life. A variety of factors are known to influence the gut microbiota, including mode of delivery of neonate, host genetic factors, hose immune response, diet, xenobiotics and other drugs, infections, and environmental microbial exposures.

    The diagnosis of gastroesophageal reflux disease in the infant population has increased during the past two decades. Acid suppression medications are used commonly in infants for gastroesophageal reflux disease and other acid-related conditions despite little evidence of their efficacy. Multiple studies have shown adverse effects in pediatric patients using either proton pump inhibitors or H2 receptor antagonists, the two classes of acid suppression medications that are most frequently used in children. Some of these adverse effects may result from alterations in the microbiome caused by these medications. Prior studies have demonstrated significant changes in microbial composition of both gastric and intestinal microbiota with proton pump inhibitor use (5), but to the investigators' knowledge, no prior studies have looked at the effect of H2 receptor antagonists on the microbiome in healthy, full term infants.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    12 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Cross-Sectional
    Official Title:
    Effect of Histamine-2 Receptor Antagonists on the Microbiome of Full Term Infants
    Actual Study Start Date :
    Aug 13, 2018
    Actual Primary Completion Date :
    Apr 30, 2019
    Actual Study Completion Date :
    Jul 31, 2019

    Arms and Interventions

    Arm Intervention/Treatment
    Control Infants

    Infants ages 2 months to 12 months who are not on H2RA medication.

    Treated Infants

    Infants ages 2 months to 12 months who are taking H2RA medication.

    Outcome Measures

    Primary Outcome Measures

    1. Microbiome taxa [At time of sampling - once at enrollment]

      16S Metagenomic taxonomy of gut microbiome

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    2 Months to 12 Months
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Full term, at least 2 months of age

    • No exposure OR at least 14 days of exposure to H2-receptor antagonist medication

    • No exposure to probiotics or antibiotics

    Exclusion Criteria:
    • Current or recent (within the past 14 days) gastrointestinal infection (viral, bacterial, or fungal)

    • Gastrointestinal mucosal disease, or have clinically significant constipation

    • Any history of exposure to proton pump inhibitors

    • Unvaccinated infants

    • Infants with weight-for-length either below the 3rd percentile for age or above the 97th percentile for age

    • Infants with rapid weight gain, defined as change in weight-for-length z-score exceeding +0.67 from birth to 4 months of age or birth to 6 months of age

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Alfred I. duPont Hospital for Children Wilmington Delaware United States 19803

    Sponsors and Collaborators

    • Nemours Children's Clinic

    Investigators

    • Principal Investigator: Matthew Di Guglielmo, MD PhD, Nemours

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Nemours Children's Clinic
    ClinicalTrials.gov Identifier:
    NCT03747991
    Other Study ID Numbers:
    • 1231469
    First Posted:
    Nov 20, 2018
    Last Update Posted:
    Aug 21, 2019
    Last Verified:
    Aug 1, 2019
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Nemours Children's Clinic
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 21, 2019