Time-Dependent Effects of Aspirin on Blood Pressure and Morning Platelet Reactivity: A Randomized Cross-Over Trial
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 an...
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Veröffentlicht in: | Hypertension (Dallas, Tex. 1979) Tex. 1979), 2015-04, Vol.65 (4), p.743-750 |
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creator | Bonten, Tobias N Snoep, Jaapjan D Assendelft, Willem J.J Zwaginga, Jaap Jan Eikenboom, Jeroen Huisman, Menno V Rosendaal, Frits R van der Bom, Johanna G |
description | 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. |
doi_str_mv | 10.1161/HYPERTENSIONAHA.114.04980 |
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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.</description><identifier>ISSN: 0194-911X</identifier><identifier>EISSN: 1524-4563</identifier><identifier>DOI: 10.1161/HYPERTENSIONAHA.114.04980</identifier><identifier>PMID: 25691622</identifier><language>eng</language><publisher>United States: American Heart Association, Inc</publisher><subject>Adolescent ; Adult ; Aged ; Aspirin - administration & dosage ; Blood Pressure - drug effects ; Blood Pressure - physiology ; Cardiovascular Diseases - blood ; Cardiovascular Diseases - prevention & control ; Circadian Rhythm ; Cross-Over Studies ; Drug Administration Schedule ; Female ; Follow-Up Studies ; Humans ; Male ; Middle Aged ; Patient Compliance ; Platelet Activation - drug effects ; Platelet Aggregation Inhibitors - administration & dosage ; Prospective Studies ; Secondary Prevention - methods ; Single-Blind Method ; Surveys and Questionnaires ; Time Factors ; Treatment Outcome ; Young Adult</subject><ispartof>Hypertension (Dallas, Tex. 1979), 2015-04, Vol.65 (4), p.743-750</ispartof><rights>2015 American Heart Association, Inc</rights><rights>2015 American Heart Association, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3710-66e2d95e52eade9cef5cced606bfbe82f5744f07997088eacfdb77fe4da4fbea3</citedby><cites>FETCH-LOGICAL-c3710-66e2d95e52eade9cef5cced606bfbe82f5744f07997088eacfdb77fe4da4fbea3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,3674,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25691622$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bonten, Tobias N</creatorcontrib><creatorcontrib>Snoep, Jaapjan D</creatorcontrib><creatorcontrib>Assendelft, Willem J.J</creatorcontrib><creatorcontrib>Zwaginga, Jaap Jan</creatorcontrib><creatorcontrib>Eikenboom, Jeroen</creatorcontrib><creatorcontrib>Huisman, Menno V</creatorcontrib><creatorcontrib>Rosendaal, Frits R</creatorcontrib><creatorcontrib>van der Bom, Johanna G</creatorcontrib><title>Time-Dependent Effects of Aspirin on Blood Pressure and Morning Platelet Reactivity: A Randomized Cross-Over Trial</title><title>Hypertension (Dallas, Tex. 1979)</title><addtitle>Hypertension</addtitle><description>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.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aspirin - administration & dosage</subject><subject>Blood Pressure - drug effects</subject><subject>Blood Pressure - physiology</subject><subject>Cardiovascular Diseases - blood</subject><subject>Cardiovascular Diseases - prevention & control</subject><subject>Circadian Rhythm</subject><subject>Cross-Over Studies</subject><subject>Drug Administration Schedule</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Patient Compliance</subject><subject>Platelet Activation - drug effects</subject><subject>Platelet Aggregation Inhibitors - administration & dosage</subject><subject>Prospective Studies</subject><subject>Secondary Prevention - methods</subject><subject>Single-Blind Method</subject><subject>Surveys and Questionnaires</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><subject>Young Adult</subject><issn>0194-911X</issn><issn>1524-4563</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkMFOGzEQhq2KClLgFZB747LB3tjeuFIPS5oSJCBRSKX2tHLWYzD1rlPbC6JP36UBDpw4jTT6_vlHH0KfKRlSKujJ7NdiulxNr67P51flrOyXbEiYHJMPaEB5zjLGxWgHDQiVLJOU_txDn2K8I4QyxopdtJdzIanI8wEKK9tA9g020GpoE54aA3WK2Btcxo0NtsW-xafOe40XAWLsAmDVanzpQ2vbG7xwKoGDhJeg6mTvbXr8gku87Bnf2L-g8ST4GLP5PQS8Cla5A_TRKBfh8Hnuox_fp6vJLLuYn51PyousHhWUZEJAriUHnoPSIGswvK5BCyLWZg3j3PCCMUMKKQsyHvflRq-LwgDTivWAGu2j4-3dTfB_OoipamyswTnVgu9iRYUYCc4FyXtUbtH66dcAptoE26jwWFFSPSmv3ijvl6z6r7zPHj3XdOsG9GvyxXEPfN0CD94lCPG36x4gVLegXLp9R8E_A-yUxA</recordid><startdate>201504</startdate><enddate>201504</enddate><creator>Bonten, Tobias N</creator><creator>Snoep, Jaapjan D</creator><creator>Assendelft, Willem J.J</creator><creator>Zwaginga, Jaap Jan</creator><creator>Eikenboom, Jeroen</creator><creator>Huisman, Menno V</creator><creator>Rosendaal, Frits R</creator><creator>van der Bom, Johanna G</creator><general>American Heart Association, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201504</creationdate><title>Time-Dependent Effects of Aspirin on Blood Pressure and Morning Platelet Reactivity: A Randomized Cross-Over Trial</title><author>Bonten, Tobias N ; Snoep, Jaapjan D ; Assendelft, Willem J.J ; Zwaginga, Jaap Jan ; Eikenboom, Jeroen ; Huisman, Menno V ; Rosendaal, Frits R ; van der Bom, Johanna G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3710-66e2d95e52eade9cef5cced606bfbe82f5744f07997088eacfdb77fe4da4fbea3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aspirin - administration & dosage</topic><topic>Blood Pressure - drug effects</topic><topic>Blood Pressure - physiology</topic><topic>Cardiovascular Diseases - blood</topic><topic>Cardiovascular Diseases - prevention & control</topic><topic>Circadian Rhythm</topic><topic>Cross-Over Studies</topic><topic>Drug Administration Schedule</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Patient Compliance</topic><topic>Platelet Activation - drug effects</topic><topic>Platelet Aggregation Inhibitors - administration & dosage</topic><topic>Prospective Studies</topic><topic>Secondary Prevention - methods</topic><topic>Single-Blind Method</topic><topic>Surveys and Questionnaires</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bonten, Tobias N</creatorcontrib><creatorcontrib>Snoep, Jaapjan D</creatorcontrib><creatorcontrib>Assendelft, Willem J.J</creatorcontrib><creatorcontrib>Zwaginga, Jaap Jan</creatorcontrib><creatorcontrib>Eikenboom, Jeroen</creatorcontrib><creatorcontrib>Huisman, Menno V</creatorcontrib><creatorcontrib>Rosendaal, Frits R</creatorcontrib><creatorcontrib>van der Bom, Johanna G</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Hypertension (Dallas, Tex. 1979)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bonten, Tobias N</au><au>Snoep, Jaapjan D</au><au>Assendelft, Willem J.J</au><au>Zwaginga, Jaap Jan</au><au>Eikenboom, Jeroen</au><au>Huisman, Menno V</au><au>Rosendaal, Frits R</au><au>van der Bom, Johanna G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Time-Dependent Effects of Aspirin on Blood Pressure and Morning Platelet Reactivity: A Randomized Cross-Over Trial</atitle><jtitle>Hypertension (Dallas, Tex. 1979)</jtitle><addtitle>Hypertension</addtitle><date>2015-04</date><risdate>2015</risdate><volume>65</volume><issue>4</issue><spage>743</spage><epage>750</epage><pages>743-750</pages><issn>0194-911X</issn><eissn>1524-4563</eissn><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.</abstract><cop>United States</cop><pub>American Heart Association, Inc</pub><pmid>25691622</pmid><doi>10.1161/HYPERTENSIONAHA.114.04980</doi><tpages>8</tpages></addata></record> |
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subjects | Adolescent Adult Aged Aspirin - administration & dosage Blood Pressure - drug effects Blood Pressure - physiology Cardiovascular Diseases - blood Cardiovascular Diseases - prevention & control Circadian Rhythm Cross-Over Studies Drug Administration Schedule Female Follow-Up Studies Humans Male Middle Aged Patient Compliance Platelet Activation - drug effects Platelet Aggregation Inhibitors - administration & dosage Prospective Studies Secondary Prevention - methods Single-Blind Method Surveys and Questionnaires Time Factors Treatment Outcome Young Adult |
title | Time-Dependent Effects of Aspirin on Blood Pressure and Morning Platelet Reactivity: A Randomized Cross-Over Trial |
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