Skip to main content
OpenTrials
Completed

NCT Number: NCT00779870

Airway Smooth Muscle and Asthma Severity

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.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Royal Brompton Hospital

London, Sw3 6NP, United Kingdom

About this study

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:

  • 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

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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)
  • Requirement for daily treatment with a controller medication in addition to ICS e.g. LABA, theophylline, leukotriene antagonist
  • Asthma symptoms requiring SABA on a daily or near daily basis
  • Persistent airways obstruction (FEV1 <80% predicted, diurnal PEF variation >20%)
  • One or more emergency care visits for asthma per year
  • 3 or more steroid "bursts" per year
  • Prompt deterioration with ≤ 25% reduction in oral or ICS
  • 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

Exclusion criteria

History of asthma or allergic rhinitis Any chronic illness Current smokers, or less than 3 years since quitting smoking (< 5 pack/years) PC20 less than 16mg/ml On anti-platelet or anti-coagulant drugs Low platelet count Pregnancy or breast-feeding Previous bronchoscopy within three months of this study

Treatment and study plan

Bronchoscopy

Other

bronchoscopy under local anaesthetic and sedation to obtain endobronchial biopsies

Primary outcomes

  1. Difference in ASM Mass Between Groups

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

  2. Difference in ASM Proliferation, Migration and Cytokine Release Between Groups

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

  3. Difference in Intracellular Oxidative Stress Mechanisms From ASM Between Groups

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

    Expression of Nrf2 protein

Secondary outcomes

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

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

Sponsors and collaborators

Lead sponsor

Imperial College London

Other

Collaborators

  • Asthma UK
  • Royal Brompton & Harefield NHS Foundation Trust

Registry information

Official study title

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

Important dates

Study start
2008
Primary completion
2012
Study completion
2012
First posted
Oct 24, 2008
Registry last updated
Oct 31, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.