Coronary Heart Disease Clinical Trial
Official title:
The Effects of Air Pollution on Vascular and Endogenous Fibrinolytic Function in Patients With Coronary Heart Disease
Air pollution is a major cause of cardiovascular morbidity and mortality. The components of air pollution responsible and the mechanisms through which they might mediate these harmful effects remain only partially understood. We hypothesise that these adverse effects are mediated by combustion derived air pollutants and that even a brief exposure will effect heart and blood vessel function. We assess the effect of dilute diesel exhaust inhalation at levels encountered in urban road traffic on heart and blood vessel function in patients with stable coronary heart disease.
Observational studies suggest that exposure to air pollution may worsen symptoms of angina
and trigger acute myocardial infarction. These findings are limited by imprecision in the
measurement of pollution exposure, the effect of potential confounding environmental and
social factors, and the lack of mechanistic data. Controlled exposures of air pollutants can
help to address these shortcomings by providing a precisely defined exposure in a regulated
environment that facilitates investigation with validated biomarkers and surrogate measures
of cardiovascular health. Using a carefully characterised exposure system, we have
previously shown in healthy volunteers that exposure to dilute diesel exhaust causes lung
inflammation, depletion of airway antioxidant defences, and impairment of vascular and
fibrinolytic function. To date, there have been no controlled exposures in patients with
coronary heart disease: an important population who may be particularly susceptible to the
adverse cardiovascular effects of air pollution.
In a double blind randomized cross-over study, 20 patients with prior myocardial infarction
will be exposed to dilute diesel exhaust (300µg/m3) or filtered air during periods of rest
and moderate exercise in a controlled exposure facility. During the exposure, myocardial
ischemia will be quantified by ST-segment analysis using continuous 12-lead
electrocardiography. Six hours following exposure, vascular vasomotor and fibrinolytic
function will be assessed by means of intra-arterial agonist infusions.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double-Blind, Primary Purpose: Prevention
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