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Airway Smooth Muscle and Asthma Severity

Evaluating the Role of Oxidant/Anti-oxidant Balance and the Relationship of Asthma Severity on Airway Smooth Muscle Proliferation, Migration and Cytokine Release.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00779870
Enrollment
18
Registered
2008-10-24
Start date
2008-10-31
Completion date
2012-09-30
Last updated
2019-10-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Asthma

Keywords

asthma severity, airway smooth muscle, oxidative stress

Brief summary

Our hypothesis is that the severity of asthma is determined by the way in which airway smooth muscle cells grow and release inflammatory mediators. Our main objective is to establish how the properties of the airway smooth muscle cell varies with asthma severity. Environmental agents, such as cigarette smoke, and inflammation can give rise to oxidative stress - this is a process whereby harmful chemicals called free radicals are formed in the body and damage tissues. The damage caused can be limited/prevented by protective, or anti-oxidant mediators. We will also look at molecules involved in oxidative stress which may affect the way in which the airway smooth muscle grows and produces inflammatory mediators.

Detailed description

Aims and Objectives The objective of this study is to examine whether the severity of asthma is related to (and possibly caused by) ASM dysfunction. Severe asthmatics have been shown to have more ASM in bronchial biopsies than non-severe asthmatics16. Because ASM cells can be obtained from bronchial biopsies obtained via bronchoscopy, we will examine endobronchial biopsies from mild, moderate and severe asthmatics, and healthy non-asthmatic subjects to compare features of remodelling (severe asthmatic subjects will have been assessed through the Difficult Asthma Protocol at the Royal Brompton Hospital24). In particular, we will focus on ASM mass, proliferation and changes in expression of different contractile proteins (α-actin and myosin) and chemokines, and will assess in vitro the response of ASM cells to stimulation by TGF-β and IL-1β. We will also examine the effect of dexamethasone on chemokine release and induced proliferation in vitro. We will also study enzymes and anti-oxidants involved in oxidative stress, such as Nox4, MnSOD and catalase, to look at their role in regulating ASM cell proliferation and chemokine synthesis. We want to see if there is an oxidant-anti oxidant balance in ASM in severe asthma compared to non-severe asthma. AIM: 1\. To establish the difference in ASM phenotype in asthma patients of differing severity of disease in terms of ASM mass, proliferation, migration and chemokine release. Study design There will be 3 study visits. In the first two visits, the subjects will undergo spirometry with reversibility testing, a methacholine challenge test (to assess degree of bronchial hyper-responsiveness), skin prick tests and IgE levels (to assess atopic status), measurement of exhaled nitric oxide (as a non-invasive marker of inflammation), and the asthmatic subjects will complete an Asthma Control Questionnaire and an Asthma Quality of Life Questionnaire. The third visit will be on the day admission for the bronchoscopy. Study protocol: Visit 1 - screening visit * Explain purpose of study- address any queries/concerns * History and examination * Skin prick tests * Blood test for full blood count, clotting profile and IgE * Measurement of exhaled nitric oxide (eNO) * Spirometry pre and post β agonist * Completion of Asthma Control Questionnaire and * Completion of Asthma Quality of Life Questionnaire Visit 2 - Methacholine challenge test Visit 3 - Day admission for fibreoptic bronchoscopy

Interventions

OTHERbronchoscopy

bronchoscopy under local anaesthetic and sedation to obtain endobronchial biopsies

Sponsors

Asthma UK
CollaboratorOTHER
Royal Brompton & Harefield NHS Foundation Trust
CollaboratorOTHER
Imperial College London
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

- Asthma Age 18-60 Physician diagnosis of asthma Intermittent/mild, moderate and severe asthma as per GINA guidelines \[1\] For the severe asthma subjects, they will also have the following: Major characteristics (at least one of the following criteria) * Treatment with continuous or near continuous (\>50% of year) oral corticosteroids * Requirement for treatment with high dose inhaled corticosteroids (ICS) Minor characteristics (at least 2 out of the following) 1. Requirement for daily treatment with a controller medication in addition to ICS e.g. LABA, theophylline, leukotriene antagonist 2. Asthma symptoms requiring SABA on a daily or near daily basis 3. Persistent airways obstruction (FEV1 \<80% predicted, diurnal PEF variation \>20%) 4. One or more emergency care visits for asthma per year 5. 3 or more steroid bursts per year 6. Prompt deterioration with ≤ 25% reduction in oral or ICS 7. Near fatal asthma event in the past Reference \[1\] GINA - The Global Initiative for Asthma. www.ginasthma.com

Exclusion criteria

- Asthma Intubation for asthma within 6 months of entry into this study Current smokers, or less than 3 years since quitting smoking (\< 5 pack/years) Less than 4 weeks from an exacerbation On steroid-sparing agent or immunosuppressant such as azathioprine, methotrexate and ciclosporin Concomitant anti-IgE therapy On anti-platelet or anti-coagulant drugs Low platelet count Pregnancy or breast-feeding Previous bronchoscopy within three months of this study Healthy volunteer subjects: We are aiming for 5 atopic and 5 non-atopic healthy volunteers. Inclusion criteria: Age 18 - 60 Non smokers (or less than 5 pack/yrs if ex-smokers) Normal lung function

Design outcomes

Primary

MeasureTime frameDescription
Difference in ASM Mass Between Groupsat time of bronchoscopy, an average of 1 hour
Difference in ASM Proliferation, Migration and Cytokine Release Between Groupsat time of bronchoscopy, an average of 1 hour
Difference in Intracellular Oxidative Stress Mechanisms From ASM Between Groupsat time of bronchoscopy, an average of 1 hourExpression of Nrf2 protein

Secondary

MeasureTime frame
Correlation Between ASM Mass and Airway Hyper-responsiveness (PC20)at the time of bronchoscopy, an average of 1 hour

Countries

United Kingdom

Participant flow

Pre-assignment details

Results of the low number of participants the mild and moderate asthma patients were combined to Non severe group

Participants by arm

ArmCount
Healthy
Healthy Participant
5
Non-severe Asthma
Patients with mild and moderate asthma
6
Severe Asthma
Patients with severe asthma
7
Total18

Baseline characteristics

CharacteristicNon-severe AsthmaSevere AsthmaTotalHealthy
Age, Continuous38.17 years
STANDARD_DEVIATION 8.5
36.67 years
STANDARD_DEVIATION 4.12
36.5 years
STANDARD_DEVIATION 6.3
34.67 years
STANDARD_DEVIATION 6.3
Race and Ethnicity Not Collected0 Participants
Region of Enrollment
United Kingdom
6 participants7 participants18 participants5 participants
Sex: Female, Male
Female
1 Participants2 Participants4 Participants1 Participants
Sex: Female, Male
Male
5 Participants4 Participants11 Participants2 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
deaths
Total, all-cause mortality
0 / 50 / 60 / 7
other
Total, other adverse events
0 / 50 / 60 / 7
serious
Total, serious adverse events
0 / 50 / 60 / 7

Outcome results

Primary

Difference in ASM Mass Between Groups

Time frame: at time of bronchoscopy, an average of 1 hour

Population: No data collected

Primary

Difference in ASM Proliferation, Migration and Cytokine Release Between Groups

Time frame: at time of bronchoscopy, an average of 1 hour

Population: Data not collected

Primary

Difference in Intracellular Oxidative Stress Mechanisms From ASM Between Groups

Expression of Nrf2 protein

Time frame: at time of bronchoscopy, an average of 1 hour

ArmMeasureValue (MEAN)
HealthyDifference in Intracellular Oxidative Stress Mechanisms From ASM Between Groups2 relative expression unit
Non-severe AsthmaDifference in Intracellular Oxidative Stress Mechanisms From ASM Between Groups3 relative expression unit
Severe AsthmaDifference in Intracellular Oxidative Stress Mechanisms From ASM Between Groups3 relative expression unit
p-value: 0.06t-test, 2 sided
p-value: 0.8t-test, 2 sided
Secondary

Correlation Between ASM Mass and Airway Hyper-responsiveness (PC20)

Time frame: at the time of bronchoscopy, an average of 1 hour

Population: No data collected

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026