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Published on: February 3, 2021
Evaluation of an abbreviated adenosine monophosphate bronchial challenge
Tom C Fardon1, Melissa R Hodge, Brian J Lipworth
1Asthma and Allergy Research Group, University of Dundee, Ninewells Hospital and Medical School, Dundee, DD1 9SY, UK.
Rationale:
Airway hyperresponsiveness to adenosine monophosphate (AMP) has been validated as a surrogate marker for airway inflammation. We wished to know whether an abbreviated challenge at the final threshold dose would produce the same fall in FEV1 as a full, conventional dose-response challenge.
Methods:
Seventeen patients with mild-to-moderate asthma (mean FEV1, 75.5% predicted) attended for a full dose-response protocol, where the highest concentration of AMP to produce > 20% fall in FEV1 was noted, along with the maximum percentage fall and recovery time. Patients returned within 2 days for a further challenge, when they received only the highest concentration (as a single bolus) reached on the previous visit.
Results:
The mean (+/- SEM) percentage fall in FEV1 after the full challenge was 25.5 +/- 1.3%, and after the abbreviated challenge was 9.4 +/- 2.4%. The mean recovery after the full challenge was 28.13 +/- 4.65 min, and after the abbreviated test was 10.81 +/- 4.27 min.
Conclusion:
An abbreviated challenge using a single bolus dose of AMP grossly underestimates bronchial hyperresponsiveness. Although the pharmacologic half-life of AMP is short (90 s), the lesser response and shortened recovery with the abbreviated challenge suggest a more prolonged physiologic half-life, which in turn may have implications for abbreviated challenge protocols.
Insights
An abbreviated adenosine monophosphate (AMP) challenge test underestimates bronchial hyperresponsiveness compared to a full dose-response test. This suggests a longer physiological effect than its short pharmacological half-life implies.
Area of Science:
- Pulmonary Medicine
- Respiratory Physiology
Background:
- Airway hyperresponsiveness to adenosine monophosphate (AMP) is a validated marker for airway inflammation.
- Conventional dose-response challenges are used to assess this hyperresponsiveness.
Purpose of the Study:
- To determine if an abbreviated AMP challenge at the threshold dose replicates the FEV1 fall of a full dose-response challenge.
- To investigate the implications of abbreviated challenge protocols for assessing bronchial hyperresponsiveness.
Main Methods:
- Seventeen patients with mild-to-moderate asthma underwent a full AMP dose-response challenge to identify the threshold dose.
- A subsequent abbreviated challenge administered only the threshold AMP concentration as a single bolus.
Main Results:
- The full challenge resulted in a mean FEV1 fall of 25.5%, while the abbreviated challenge caused a 9.4% fall.
- Mean recovery time was 28.13 minutes after the full challenge and 10.81 minutes after the abbreviated challenge.
Conclusions:
- An abbreviated AMP challenge significantly underestimates bronchial hyperresponsiveness.
- The prolonged physiological effect, despite AMP's short pharmacological half-life, has implications for abbreviated challenge test design.
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