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Published on: November 8, 2024
Time-dependent effects of aspirin on blood pressure and morning platelet reactivity: a randomized cross-over trial
Tobias N Bonten1, Jaapjan D Snoep2, Willem J J Assendelft2
1From the Department of Clinical Epidemiology, Leiden University Medical Center, Leiden, the Netherlands (T.N.B., J.D.S., F.R.R., J.G.v.d.B.); Department of Primary and Community Care, Radboud University Medical Center, Nijmegen, the Netherlands (W.J.J.A.); Department of Public Health and Primary Care, Leiden University Medical Center, Leiden, the Netherlands (W.J.J.A.); JJ van Rood Center for Clinical Transfusion Research, Sanquin Research, Leiden, the Netherlands (J.J.Z., J.G.v.d.B.); and Department of Thrombosis and Hemostasis, Leiden University Medical Center, Leiden, the Netherlands (J.E., M.V.H.). t.n.bonten@lumc.nl.
Insights
Taking low-dose aspirin at bedtime did not lower blood pressure in cardiovascular disease patients. However, bedtime aspirin did reduce morning platelet reactivity, potentially lowering cardiovascular event risk during high-risk morning hours.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Trials
Background:
- Daily aspirin intake is common for cardiovascular disease (CVD) prevention.
- Previous research suggested bedtime aspirin may lower blood pressure.
- Morning hours are associated with peak platelet reactivity and CVD events.
Purpose of the Study:
- To investigate the effect of bedtime aspirin versus morning aspirin on 24-hour blood pressure and morning platelet reactivity in CVD patients.
- To determine if timing of aspirin intake influences cardiovascular risk markers.
Main Methods:
- Randomized, open-label, crossover trial involving 290 patients with CVD.
- Patients took 100 mg aspirin at bedtime or on awakening for 3-month periods.
- Measurements included 24-hour ambulatory blood pressure and morning platelet reactivity.
Main Results:
- Bedtime aspirin did not significantly reduce systolic or diastolic blood pressure compared to morning intake.
- Aspirin taken at bedtime significantly reduced morning platelet reactivity by -22 aspirin reaction units.
- The findings were based on primary analysis populations of 263 for blood pressure and 133 for platelet reactivity.
Conclusions:
- Taking low-dose aspirin at bedtime does not lower blood pressure in patients with CVD.
- Bedtime aspirin intake effectively reduces morning platelet reactivity.
- Further research is warranted to evaluate if this timing strategy reduces morning cardiovascular events.
Abstract:
Aspirin is used for cardiovascular disease (CVD) prevention by millions of patients on a daily basis. Previous studies suggested that aspirin intake at bedtime reduces blood pressure compared with intake on awakening. This has never been studied in patients with CVD. Moreover, platelet reactivity and CVD incidence is highest during morning hours. Bedtime aspirin intake may attenuate morning platelet reactivity. This clinical trial examined the effect of bedtime aspirin intake compared with intake on awakening on 24-hour ambulatory blood pressure measurement and morning platelet reactivity in patients using aspirin for CVD prevention. In this randomized open-label crossover trial, 290 patients were randomized to take 100 mg aspirin on awakening or at bedtime during 2 periods of 3 months. At the end of each period, 24-hour blood pressure and morning platelet reactivity were measured. The primary analysis population comprised 263 (blood pressure) and 133 (platelet reactivity) patients. Aspirin intake at bedtime did not reduce blood pressure compared with intake on awakening (difference systolic/diastolic: -0.1 [95% confidence interval, -1.0, 0.9]/-0.6 [95% confidence interval, -1.2, 0.0] mm Hg). Platelet reactivity during morning hours was reduced with bedtime aspirin intake (difference: -22 aspirin reaction units [95% confidence interval, -35, -9]). The intake of low-dose aspirin at bedtime compared with intake on awakening did not reduce blood pressure of patients with CVD. However, bedtime aspirin reduced morning platelet reactivity. Future studies are needed to assess the effect of this promising simple intervention on the excess of cardiovascular events during the high risk morning hours.
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