Contributing Factors in the Pathobiology of Airway Remodeling in Obesity



Status:Recruiting
Conditions:Asthma, Asthma, Obesity Weight Loss
Therapuetic Areas:Endocrinology, Pulmonary / Respiratory Diseases
Healthy:No
Age Range:18 - 60
Updated:9/14/2018
Start Date:April 9, 2018
End Date:April 13, 2024
Contact:Loretta Que, MD
Email:loretta.que@duke.edu
Phone:919-684-8111

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There are two aims for this study. The purpose of this study is to determine the effects of
body weight and hormones on airway fibrosis (scarring) and lung function in obese & lean
asthma subjects compared to obese & lean non-asthma subjects (Aim 1). And in obese subjects
with asthma undergoing bariatric surgery compared to obese non-asthma subjects undergoing
bariatric surgery (Aim 2).


Inclusion Criteria:

Obese asthmatic & lean asthmatic

1. Outpatient adults of either sex 18-60 years of age with an initial asthma diagnosis at
< 12 years of age, as defined by the NHLBI NAEPP guidelines.

2. Lean subjects with body mass index (BMI) ≥ 20 kg/m2 and < 30 kg/m2 or obese subjects
with BMI ≥ 30 and ≤ 50 kg/m2

3. Physician diagnosis of asthma

4. FEV1 within acceptable limits (>45% predicted before and >55% predicted after,
bronchodilator administration).

5. Negative pregnancy test in women of childbearing potential (confirmed during
screening).

6. Relatively healthy subjects able to undergo bronchoscopy without complications.

7. Willing and able to give informed consent and adhere to visit/protocol schedules.

8. Read and write in English.

Obese non-asthmatic & Lean non-asthmatic

1. Outpatient adults of either sex 18-60 years of age.

2. Lean subjects with body mass index (BMI) ≥ 20 kg/m2 and < 30 kg/m2 or obese subjects
with BMI ≥ 30 and ≤ 50 kg/m2

3. Negative pregnancy test in women of childbearing potential (confirmed during
screening).

4. Normal lung function.

5. No clinical history of atopy.

6. No significant medical or psychological issues.

7. Healthy subjects able to undergo bronchoscopy without complications.

8. Willing and able to give informed consent and adhere to visit/protocol schedules.

9. Read and write in English.

Asthmatic undergoing bariatric surgery

1. Outpatient adults of either sex 18-60 years of age with an initial asthma diagnosis at
< 12 years of age, as defined by the NHLBI NAEPP guidelines.

2. Physician diagnosis of asthma

3. FEV1 within acceptable limits (>45% predicted before and >55% predicted after,
bronchodilator administration).

4. Morbidly obese subjects undergoing gastric bypass or sleeve gastrectomy and receiving
care at the Duke Metabolic and Weight Loss Surgery Center.

5. Negative pregnancy test in women of childbearing potential (confirmed during
screening).

6. Relatively healthy subjects able to undergo bronchoscopy without complications.

7. Willing and able to give informed consent and adhere to visit/protocol schedules.

8. Read and write in English.

Non-Asthmatic undergoing bariatric surgery

1. Outpatient adults of either sex 18-60 years of age.

2. Morbidly obese subjects undergoing gastric bypass or sleeve gastrectomy and receiving
care at the Duke Metabolic and Weight Loss Surgery Center.

3. Negative pregnancy test in women of childbearing potential (confirmed during
screening).

4. Normal lung function.

5. No clinical history of atopy.

6. No significant medical or psychological issues.

7. Healthy subjects able to undergo bronchoscopy without complications.

8. Willing and able to give informed consent and adhere to visit/protocol schedules.

9. Read and write in English.

Exclusion Criteria:

1. Children < 18 years of age.

2. Adults ≥ 18 years of age with an initial asthma diagnosis at ≥ 12 years of age, as
defined by the NHLBI NAEPP guidelines.

3. Inpatient status.

4. FEV1 is less than 45% predicted before, or less than 55% predicted after,
bronchodilator administration.

5. Upper or lower respiratory tract infection within one month of the study.

6. Use of inhaled or systemic corticosteroids within four weeks of study.

7. Use of long-acting beta-2, GLP-1R agonists, or dipeptidyl peptidase-4 (DPP-4)
inhibitors within two weeks of study.

8. Smoking history > 5 pack years or any cigarette use within the previous six months.

9. Significant non-asthma pulmonary disease (stable obstructive sleep apnea is not
excluded).

10. Positive pregnancy test for women and/or nursing women.

11. An ED visit or inpatient admission for a primary respiratory diagnosis or treatment
with antibiotics within 60 days of enrollment.

12. Poorly controlled concomitant conditions that pose additional procedure risk as
determined by the investigator.

13. Uncontrolled sleep apnea
We found this trial at
2
sites
Durham, North Carolina 27704
Principal Investigator: Loretta Que
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407 Crutchfield Street
Durham, North Carolina 27704
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Durham, NC
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