Clinical Research
Chronic Coronary Disease
Platelet Response to Low-Dose Enteric-Coated Aspirin in Patients With Stable Cardiovascular Disease

https://doi.org/10.1016/j.jacc.2005.06.058Get rights and content
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Objectives

We investigated whether use of low-dose enteric-coated (EC) aspirin for secondary prevention of cardiovascular events has sufficient bioavailability to achieve complete platelet cyclooxygenase (COX) inhibition in all individuals.

Background

Aspirin reduces cardiovascular morbidity and mortality in patients with pre-existing vascular disease; however, there is variability in the way individuals respond. Persistent normal platelet function despite therapy, referred to as “aspirin resistance,” is associated with an increased risk of major cardiovascular events.

Methods

We studied 131 stable cardiovascular patients between March and September 2002 who were taking 75 mg EC aspirin. Serum thromboxane (TX) B2levels were assayed as a measure of COX activity. Mean arachidonic acid (AA)-induced platelet aggregation ≥20% was deemed evidence of persistent platelet activity and an incomplete aspirin response.

Results

Patients of median age 63 years (61% men) were enrolled. Forty-four percent of patients had elevated serum TX B2levels (>2.2 ng/ml). Arachidonic acid-induced platelet aggregation occurred more frequently in these patients (21% vs. 3%; p = 0.004). In all cases addition of exogenous aspirin during the assay abolished platelet aggregation. Patient weight and age were significant independent predictors of an incomplete response to EC aspirin (p = 0.025 and p < 0.001, respectively). These patients were also more likely to have a history of myocardial infarction (MI) (p = 0.038).

Conclusions

Many patients who are prescribed low-dose EC aspirin for secondary prevention of cardiovascular events have persistent uninhibited platelet COX activity. Younger and heavier patients and those with a previous MI are most likely to have an inadequate response to treatment.

Abbreviations and Acronyms

AA
arachidonic acid
COX
cyclooxygenase
EC
enteric-coated
MI
myocardial infarction
NSAIDs
non-steroidal anti-inflammatory drugs
TX
thromboxane

Cited by (0)

Drs. Maree, Curtin, Cox, and Fitzgerald contributed equally to the study. The Irish Heart Foundation and the Higher Education Authority of Ireland sponsored this study.