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| ID | Type | Description | Link |
|---|---|---|---|
| R01HL164787 | U.S. NIH Grant/Contract | View source |
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| Name | Class |
|---|---|
| National Institutes of Health (NIH) | NIH |
| National Heart, Lung, and Blood Institute (NHLBI) | NIH |
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This is a single-center study of 80 subjects with asthma including those with obesity and metabolic dysfunction (MD), those with obesity and without metabolic dysfunction, those with severe asthma and mucus plugging and those with severe asthma and without mucus plugging. Screening data will be reviewed to determine participant eligibility. Participants who meet all inclusion criteria will participate in a cardiopulmonary exercise testing (CPET) visit to compare lung function markers and change in oxygen saturation between obese patients with and without MD and severe asthma patients with and without mucus plugging.
The mechanism of poor exercise tolerance in patients with severe asthma is poorly understood. In preliminary data, the investigators have identified increases in air trapping in patients with obese asthma and metabolic dysfunction and patients with asthma and mucus plugs. The investigators have also found air trapping on CT (Computerized Tomography) scans of severe asthma patients with mucus plugs. Therefore, the investigators hypothesize that obese patients with metabolic dysfunction (MD) and severe asthma patients with mucus plugs develop changes in lung function during exercise.
To test this hypothesis, this protocol will plan for cardiopulmonary exercise testing in patients with obesity or severe asthma. The analyses will compare dynamic hyperinflation, expiratory flow limitation, and the RV/TLC ratio (ratio of residual volume to total lung capacity) before and after exercise between obese patients with and without MD and severe asthma patients with and without mucus plugs.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Patients with asthma, obesity and metabolic dysfunction | Otherwise healthy asthmatic subjects with:
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| Patients with asthma, obesity and no metabolic dysfunction | Otherwise healthy asthmatic subjects with:
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| Patients with severe asthma and mucus plugs | Otherwise healthy asthmatic subjects:
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| Patients with severe asthma and no mucus plugs | Otherwise healthy asthmatic subjects:
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| Measure | Description | Time Frame |
|---|---|---|
| Change in EELV (End Expiratory Lung Volume) | We will compare change in EELV during the CPET (Cardiopulmonary Exercise Test) between the obese asthma patients with MD or without MD and between the patients with severe asthma with mucus plugs or without mucus plugs. | At CPET visit. |
| Measure | Description | Time Frame |
|---|---|---|
| Change in RV (Residual Volume) and TLC (Total Lung Capacity) | We will compare change in RV and TLC during the CPET between the obese asthma patients with MD or without MD and between the patients with severe asthma with mucus plugs or without mucus plugs. | At CPET Visit |
| Change in oxygen saturation during exercise |
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Inclusion Criteria:
1. IL-6 high: Plasma IL-6 > 3.0 pg/mL 2. Insulin resistance: HOMA-IR > 3 mass units b. Severe asthma: Requires treatment with high dose inhaled corticosteroids plus a second controller, systemic corticosteroid, or biologic therapy.
i. Mucus Plugging is defined as mucus plug score ≥ 4
Exclusion Criteria:
Asthma exacerbation or URI within the previous 6 weeks.
History of smoking
Pregnancy
Absolute or relative contraindication to exercise testing per ATS criteria
Any other criteria that place the subject at unnecessary risk according to the judgment of the Principal Investigator and/or attending physician of record.
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The study will recruit up to 80 asthma participants, at least 20 with obesity and MD, 20 with obesity and no MD, 20 with severe asthma and mucus plugs and 20 with severe asthma and no mucus plugs.
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Jade Vi, BS | Contact | 415-476-1783 | jade.vi@ucsf.edu | |
| John Fahy, MD, MS | Contact | 415-476-9940 | john.fahy@ucsf.edu |
| Name | Affiliation | Role |
|---|---|---|
| John Fahy, MD, MS | University of California, San Francisco | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| UCSF Airway Clinical Research Center | Recruiting | San Francisco | California | 94143 | United States |
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| ID | Term |
|---|---|
| D001249 | Asthma |
| ID | Term |
|---|---|
| D001982 | Bronchial Diseases |
| D012140 | Respiratory Tract Diseases |
| D008173 | Lung Diseases, Obstructive |
| D008171 | Lung Diseases |
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Samples of plasma and serum will be banked in the UCSF Airway Tissue Bank.
Change in oxygen saturation during the CPET will be assessed and compared between the obese asthma patients with MD or without MD and between the patients with severe asthma with mucus plugs or without mucus plugs. |
| At CPET Visit |
| D012130 |
| Respiratory Hypersensitivity |
| D006969 | Hypersensitivity, Immediate |
| D006967 | Hypersensitivity |
| D007154 | Immune System Diseases |