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The Genetics of Severe Asthma in Children

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ClinicalTrials.gov Identifier: NCT01238432
Recruitment Status : Active, not recruiting
First Posted : November 10, 2010
Last Update Posted : June 23, 2020
Sponsor:
Collaborator:
UConn Health
Information provided by (Responsible Party):
Christopher Carroll, MD, Connecticut Children's Medical Center

Tracking Information
First Submitted Date November 8, 2010
First Posted Date November 10, 2010
Last Update Posted Date June 23, 2020
Study Start Date October 2009
Estimated Primary Completion Date April 2025   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures
 (submitted: November 9, 2010)
The primary end point is the development of a near fatal asthma exacerbation. [ Time Frame: 3 years ]
Original Primary Outcome Measures Same as current
Change History
Current Secondary Outcome Measures
 (submitted: November 9, 2010)
The secondary end point is hospital length of stay. [ Time Frame: 3 years ]
Original Secondary Outcome Measures Same as current
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title The Genetics of Severe Asthma in Children
Official Title The Genetics of Severe Asthma in Children
Brief Summary Near fatal asthma exacerbations are one of the most common causes of critical illness in children, accounting for approximately ten thousand intensive care unit (ICU) admissions per year in the United States. Even children with intermittent or mild baseline asthma can develop these severe exacerbations; however, there are few studies evaluating the risk factors associated with the development of near fatal asthma exacerbations in children. Inhaled β2-adrenergic receptor (ADRβ2) agonist therapy is the foundation of therapy for acute asthma and genetic variations of this receptor have been shown to affect response to ADRβ2 agonist therapy in this population. The investigators hypothesis is that a child's ADRβ2 genotype is associated with the development of a near fatal asthma exacerbation.
Detailed Description

Our primary outcome measure is the development of a near fatal asthma exacerbation. Secondary outcome measures will include the duration of continuously nebulized ADRβ2 agonist therapy and the duration of IV ADRβ2 agonist therapy. Children will be stratified by ADRβ2 genotype at amino acid position 16 and outcomes compared.

We propose to investigate two separate populations in this study: (1) children admitted to the hospital with an acute asthma exacerbation, and (2) children with asthma who have never had an acute near fatal asthma exacerbation. In addition, in order to replicate findings in an independent cohort, we will examine the genotypes of a third cohort of age-matched children without asthma.

For the population of children admitted to the hospital with an acute asthma exacerbation, the following inclusion criteria will be met: (1) admission to the hospital with a primary admission diagnosis of asthma exacerbation and (2) age between 4 years and 18 years. Near fatal asthma exacerbations will be defined as (1) treatment with intubation and mechanical ventilation, (2) presence of respiratory acidosis (arterial pCO2 > 45), or (3) Modified Pulmonary Index Score > 12 after 2 hours of at least 20 mg/hour of continuously nebulized albuterol therapy. Children will be excluded if they have a (1) pre-existing chronic disease (other than asthma) including: (a) bronchopulmonary dysplasia, (b) bronchomalacia, (c) tracheomalacia, (d) laryngomalacia, (e) vocal cord dysfunction, (f) chronic restrictive lung disease, (g) recurrent aspiration pneumonia, or (h) congenital heart disease.

For the population of children with asthma who have never had an acute near fatal asthma exacerbation, the following inclusion criteria will be met: (1) diagnosis of asthma and (2) age between 4 years and 18 years. Children will be excluded if (1) that child ever required admission to the hospital for a near fatal asthma exacerbation and (2) if they have a pre-existing chronic disease (other than asthma) as listed above. We propose to enroll 158 children, recruited from Pulmonary Clinic at the study institution, matched by age, by gender, and by NHLBI asthma classification to the population of children with near fatal asthma exacerbations.

In order to replicate these findings in an independent cohort, we will also examine these genetic markers in a reference group of 80 healthy children without asthma, matched by age, gender and race/ethnicity to the group of children with near fatal asthma exacerbations. The following inclusion criteria will be met for this group: (1) age between 4 and 18 years. Children will be excluded if they have any pre-existing chronic disease. This population of children will be recruited from the Primary Care Clinic at CCMC and if necessary for racial/ethnic matching, from a private practice in suburban Hartford.

For the population of children hospitalized with an asthma exacerbation, patients will be approached, consented and enrolled upon admission to the hospital. In this observational study, patients will be treated according to the current asthma treatment protocol in effect at Connecticut Children's Medical Center. This protocol has been previously published 13 and titrates therapy based on a clinical asthma score (MPIS) 51 that has been shown to be highly reproducible between groups of physicians, nurses and respiratory therapists. This around-the-clock adjustment of therapy by nurses and respiratory therapists produces less variation in care due to non-medical reasons. This protocol includes thresholds for admission/discharge to the hospital and for admission/discharge to the ICU based on MPIS. For the populations of children with no history of a near fatal asthma exacerbation and no asthma diagnosis, patients will be approached, consented and enrolled upon confirmation of eligibility in the Pulmonary Clinic and the Primary Care Clinic.

Genotyping of the ADRβ2 gene will be performed at the University of Connecticut Health Center (UCHC) Clinical and Translational Research Core Lab. Genotyping will be performed either from saliva or from whole blood collected during routine blood sampling for clinical care. Children will be stratified based on their genotype and outcomes compared. Providers will be blinded to genotype at the time of treatment.

Study Type Observational
Study Design Observational Model: Case-Control
Time Perspective: Prospective
Target Follow-Up Duration Not Provided
Biospecimen Retention:   Samples With DNA
Description:
saliva and blood
Sampling Method Probability Sample
Study Population Children with asthma
Condition Asthma
Intervention Not Provided
Study Groups/Cohorts
  • Inpatient population
    Children with asthma who are admitted to the hospital with an exacerbation.
  • Outpatient population
    Children with asthma who have not been admitted to the hospital with an exacerbation.
  • Healthy controls
    Children without asthma or any other chronic condition.
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status Active, not recruiting
Estimated Enrollment
 (submitted: January 31, 2017)
200
Original Estimated Enrollment
 (submitted: November 9, 2010)
558
Estimated Study Completion Date April 2025
Estimated Primary Completion Date April 2025   (Final data collection date for primary outcome measure)
Eligibility Criteria

Inclusion Criteria, inpatient asthmatics:

  • Admission to study institution with a primary admission diagnosis of asthma exacerbation
  • Age between 4 and 18 years

Exclusion Criteria, inpatient asthmatics:

- Pre-existing chronic disease (other than asthma), including: i. bronchopulmonary dysplasia ii. bronchomalacia iii. tracheomalacia iv. laryngomalacia v. vocal cord dysfunction vi. chronic restrictive lung disease vii. recurrent aspiration pneumonia viii. impaired mucous clearance ix. congenital heart disease x. pulmonary hypertension

Inclusion Criteria, outpatient asthmatics:

  • Diagnosis of asthma
  • Age between 4 and 18 years

Exclusion Criteria, outpatient asthmatics:

  • Previous admission to the hospital for a near fatal asthma exacerbation
  • Pre-existing chronic disease (other than asthma) including i. bronchopulmonary dysplasia ii. bronchomalacia iii. tracheomalacia iv. laryngomalacia v. vocal cord dysfunction vi. chronic restrictive lung disease vii. recurrent aspiration pneumonia viii. impaired mucous clearance ix. congenital heart disease x. pulmonary hypertension

Inclusion Criteria, healthy controls:

- Age between 4 and 18 years

Exclusion Criteria, healthy controls:

- Pre-existing chronic disease including: i. asthma ii. bronchopulmonary dysplasia iii. bronchomalacia iv. tracheomalacia v. laryngomalacia vi. vocal cord dysfunction vii. chronic restrictive lung disease viii. recurrent aspiration pneumonia ix. impaired mucous clearance x. congenital heart disease xi. pulmonary hypertension

Sex/Gender
Sexes Eligible for Study: All
Ages 4 Years to 18 Years   (Child, Adult)
Accepts Healthy Volunteers Yes
Contacts Contact information is only displayed when the study is recruiting subjects
Listed Location Countries United States
Removed Location Countries  
 
Administrative Information
NCT Number NCT01238432
Other Study ID Numbers 08-103
Has Data Monitoring Committee No
U.S. FDA-regulated Product
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
IPD Sharing Statement
Plan to Share IPD: No
Responsible Party Christopher Carroll, MD, Connecticut Children's Medical Center
Study Sponsor Connecticut Children's Medical Center
Collaborators UConn Health
Investigators
Principal Investigator: Christopher L Carroll, MD, MS Connecticut Children's Medical Center
PRS Account Connecticut Children's Medical Center
Verification Date June 2020