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This study aims to characterise cough in severe asthma through an observational cross-sectional analysis of patients stratified by inflammatory biomarker profile using a number of subjective and objective cough measurement tools.
Full description
This study will use a combination of subjective and objective cough measures to assess the frequency of cough as well as its related morbidity in severe asthmatics. Comparisons will be made between T2-High, T2-Low and T2-intermediate patients defined using a composite biomarker profile (blood eosinophil count and FeNO) to assess the role of cough in each and these results will be compared to the transcriptomic and proteomic measurements in the RASP-UK where the same biomarker profiling is being used to define clinical sub-groups of severe asthma. This study aims to also improve characterisation of the T2-Low population and identify possible mechanisms for the pathophysiology of this group.
60 patients are expected to be recruited to the study. Patients will be provided with an information sheet and have a telephone follow-up after at least 24 hours to ask if they remain interested in participation and if so, they will then be asked back for a baseline visit.
Three groups of severe asthmatics will be recruited (as described in appropriate section) and undergo the following procedures:
Demographic details, height, weight, spirometry, FeNO and vital signs
Patient reported outcomes:
Blood samples - a sample of blood will be taken for whole blood transcriptomic and serum analyses
Citric acid cough challenge test will be used to measure cough reflex sensitivity in each phenotype.
Spontaneous sputum sample - if patients produce a sputum sample during spirometry or citric acid challenge, this will be recorded and the sample will be retained for sputum differential cell count and storage of processed soluble components.
On completing the above procedures, patients will be asked to wear a validated ambulatory cough monitor (Leicester Cough Monitor) for a 24-hour period to assess the frequency of cough and if they agree, will be fully instructed in its use.
Patients will be asked to attend a follow-up visit 2 weeks after baseline. The study procedures will remain the same as visit 1 with the exception of collection of clinical samples.
A mild/moderate population will be recruited and undergo the same procedures as the severe group in a baseline visit. No mild/moderate asthmatics will be asked to attend for a follow-up visit.
Enrollment
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Inclusion and exclusion criteria
Inclusion Criteria (Severe Asthmatics):
Ability and willingness to comply with the study procedures
Age ≥18 to ≤75 years at the time of informed consent
Severe asthma (as defined by GINA step 4/5 classification of asthma severity) after a detailed systematic assessment
History of asthma treatment with high doses of Inhaled Corticosteroids (≥1000 µg beclomethasone dipropionate daily, or equivalent) and an additional controller
Three patient groups with severe asthma will be investigated in the study and will be defined as follows:
T2-High Severe Asthmatics (Group A)
T2-Low Severe Asthmatics (Group B)
T2 - Intermediate Severe Asthmatics (Group D)
As stated above, these measurements are made at each clinic visit as part of routine care and will be available on all subjects prior to Inclusion
A chest x-ray or CT scan obtained within 12 months before the time of informed consent and showing no new pathology requiring investigation as a potential cause for their cough
Mild/moderate severe asthmatics (who have received a diagnosis of asthma from a physician and are defined as step 2/3 using the BTS/SIGN classification of severity and ACQ<1.5) aged 18-75 years inclusive will be recruited from general respiratory clinics in the Belfast HSC Trust. Patients must have the ability and willingness to comply with study procedures.
Exclusion Criteria:
Baseline FEV1 ≤50% of predicted or ≤ 1.0L
Asthma exacerbation within 28 days before the time of informed consent or during screening
Major episode of infection requiring any of the following:
For adults: Active tuberculosis (TB) requiring treatment within the 12 months before the time of informed consent (patients are also required to have no recurrence of symptoms in the 12 months following completion of TB treatment), or
Known history of severe clinically significant immunodeficiency, including, but not limited to, human immunodeficiency virus infection and/or currently receiving or have historically received intravenous Ig for treatment for immunodeficiency Note: Immunodeficiency encompasses a wide spectrum of human conditions and/or diseases. A relative IgG deficiency that is thought, but not proven, to be a feature of severe asthma would not be exclusionary for the study.
Diagnosis or history of malignancy, or current investigation for possible malignancy
Other clinically significant medical disease that is uncontrolled despite treatment or that is likely, in the opinion of the investigator, to require a change in therapy or affect the ability to participate in the study
History of alcohol, drug, or chemical abuse that would impair or risk the patient's full participation in the study, in the opinion of the investigator
Current smoker or former smoker with a smoking history of >15 pack-years A current smoker is defined as someone who has smoked one or more cigarettes per day (or marijuana or pipe or cigar) for ≥30 days within the 24 months before the time of informed consent and for whom cotinine testing is positive.
A former smoker is defined as someone who has smoked one or more cigarettes per day (or marijuana or pipe or cigar) for ≥30 days in his or her lifetime (as long as the 30-day total did not include the 24 months before the time of informed consent) and for whom cotinine testing is negative.
A pack-year is defined as the average number of packs per day times the number of years of smoking.
Initiation of or change in allergen immunotherapy within three months before the time of informed consent
Treatment with an investigational agent within 30 days of informed consent or 5 half-lives of the investigational agent, whichever is longer
Female patients who are pregnant or lactating
Primary purpose
Allocation
Interventional model
Masking
61 participants in 4 patient groups
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Data sourced from clinicaltrials.gov
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