Asthma Clinical Trial
Official title:
Exhaled Breath Condensate Biomarkers of Inflammation in Individuals With Chronic Cervical Spinal Cord Injury
The purpose of this study is to obtain markers of airway inflammation from the exhaled breath condensate (the moisture in exhaled air) for comparison to blood based markers. These markers will be compared in tetraplegic, asthmatic and able-bodied control groups. Additionally, lung function testing will be performed, and the associations between breath condensate and blood markers and pulmonary function explored between groups.
The predominant mechanism for pulmonary dysfunction in individuals with chronic tetraplegia
is respiratory muscle paralysis. This leads to inadequate ventilation and inability to clear
secretions placing these patients at a greater risk for the development of respiratory
complications. Furthermore, individuals with chronic tetraplegia exhibit baseline increases
in airway tone (bronchoconstriction), restoration of normal airway caliber following
bronchodilator administration, and non-specific airway hyperresponsiveness (AHR) following
inhalation of methacholine, histamine, an aerosolized distilled water. These findings in
persons with spinal cord injury (SCI) represent pulmonary features commonly seen in
individuals with asthma. Alternatively, airway inflammation may play a role in the
obstructive physiology observed in individuals with tetraplegia. In this population,
identification of cellular inflammation would confirm the presence of underlying
inflammation with a sputum induction. However, this method is hard to perform due to an
impaired cough.
The emerging field of exhaled breath condensate (EBC) biomarkers of inflammation offers a
non-invasive technique to define the presence of, and potentially address the contributing
factors of airway inflammation in the respiratory tract of individuals with tetraplegia. It
is thought that EBC composition reflects biochemical changes of airway lining fluid. EBC
contains a large number of mediators, including adenosine, ammonia, hydrogen peroxide
(H2O2), isoprostanes, leukotrienes, prostanoids, peptides and cytokines. Looking at exhaled
breath profiles of various biomarkers may be used to differentiate their different
pathophysiological mechanism of inflammation. In addition, measurements of some chemokines
(TNF-ά, interleukin (IL)-6) and inflammatory biomarkers (LTB4) in EBC and blood
simultaneously may help differentiate the degree of local vs. systemic inflammation.
Understanding the underlying mechanisms involved in pulmonary dysfunction observed in
persons with chronic cervical SCI may identify treatment options, such as use of inhaled
steroids. This approach would be expected to ultimately improve quality of life in affected
individuals, decreasing the rate of re-hospitalizations due to respiratory complications and
the socioeconomic burden placed on these with SCI and the health care system.
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Observational Model: Case Control, Time Perspective: Prospective
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