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Microbes and Respiratory Illnesses (MARI)

University of Wisconsin (UW) logo

University of Wisconsin (UW)

Status

Completed

Conditions

Asthma
Virus

Study type

Observational

Funder types

Other
NIH

Identifiers

NCT06059027
Protocol Version 4/30/2025 (Other Identifier)
2U19AI104317 (U.S. NIH Grant/Contract)
2023-1033
A536770 (Other Identifier)

Details and patient eligibility

About

This study is called the Microbes and Respiratory Illnesses (MARI) Study. Children growing up on farms are exposed to many types of microbes that could be beneficial. It is thought that increased exposure to certain types of microbes early in life helps to develop a healthy immune system and reduce the risk for severe common cold illnesses, breathing problems, and allergies.

Full description

Respiratory viruses, most notably rhinoviruses (RV), commonly infect school-age children during the month of September and are a well-known exposure for asthma exacerbations. Allergic sensitization is a risk factor for increased viral respiratory illness burden and wheezing. Nasal Airway Epithelial Cell (NAEC) responses to viral exposure show distinct transcriptional programs that differ in individuals with allergies or asthma. There is a growing body of evidence strongly suggesting nasal airway microbial communities enriched in several commensal bacteria are associated with protection from symptomatic RV infections. Metagenomic sequencing from previously collected nasal samples obtained at age 2 years showed distinct microbial communities and function in the Traditional agrarian (TA) Community Cohort compared to farm and non-farm children. How the early life nasal microbial community can impact risk for viral respiratory infection symptoms and NAEC biology remains an important and unresolved question. To address this important question, this proposal includes an observational study to identify patterns of nasal airway gene expression among three cohorts of school-age children that markedly differ in their susceptibility to respiratory illnesses and wheezing: children from TA/Amish communities, suburban children without asthma, and suburban children with asthma.

Enrollment

290 patients

Sex

All

Ages

4 to 12 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Participant and/or parent guardian must be able to understand and provide informed consent
  2. Children ages 4-12 years of age
  3. Cohort 1: Family is self-identified as Traditional agrarian (TA) Community member
  4. Cohort 2: Madison-area children with parental report of doctor-diagnosed asthma
  5. Cohort 3: Madison-area children with no history of asthma by parental report
  6. Cohort 4: Madison-area children who have an active respiratory illness

Exclusion criteria

  1. Inability or unwillingness of a participant to give written informed consent or comply with study protocol
  2. Chronic sinusitis (frequent sinus infections)
  3. Plans to move out of the area before completing the study
  4. Past or current medical problems or findings from physical examination or laboratory testing that are not listed above, which, in the opinion of the investigator, may pose additional risks from participation in the study, may interfere with the participant's ability to comply with study requirements or that may impact the quality or interpretation of the data obtained from the study
  5. Enrolled family member

Trial design

290 participants in 4 patient groups

TA Cohort
Description:
Traditional agrarian (TA) Community Children
Madison Cohort with Asthma
Description:
Madison-area Children with Asthma
Madison Cohort without Asthma
Description:
Madison-area Children without Asthma
Madison Cohort with Active Respiratory Illness
Description:
Madison-area children with active respiratory illness, with or without asthma

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Gina Crisafi, BS

Data sourced from clinicaltrials.gov

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