High Central Pulse Pressure Is Independently Associated With Adverse Cardiovascular Outcome: The Strong Heart Study

This study was designed to facilitate clinical use of central pulse pressure (PP). We sought to determine a value that might predict adverse outcome and thereby provide a target for assessment of intervention strategies. We previously documented that central PP more strongly relates to carotid hyper...

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Veröffentlicht in:Journal of the American College of Cardiology 2009-10, Vol.54 (18), p.1730-1734
Hauptverfasser: ROMAN, Mary J, DEVEREUX, Richard B, KIZER, Jorge R, OKIN, Peter M, LEE, Elisa T, WENYU WANG, UMANS, Jason G, CALHOUN, Darren, HOWARD, Barbara V
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container_end_page 1734
container_issue 18
container_start_page 1730
container_title Journal of the American College of Cardiology
container_volume 54
creator ROMAN, Mary J
DEVEREUX, Richard B
KIZER, Jorge R
OKIN, Peter M
LEE, Elisa T
WENYU WANG
UMANS, Jason G
CALHOUN, Darren
HOWARD, Barbara V
description This study was designed to facilitate clinical use of central pulse pressure (PP). We sought to determine a value that might predict adverse outcome and thereby provide a target for assessment of intervention strategies. We previously documented that central PP more strongly relates to carotid hypertrophy and extent of atherosclerosis and, more importantly, better predicts incident cardiovascular disease (CVD) than brachial PP. Radial applanation tonometry was performed in the third Strong Heart Study examination to determine central blood pressure. Cox regression analyses were performed using pre-specified covariates and quartiles of central and brachial PP. Among 2,405 participants without prevalent CVD, 344 suffered CVD events during 5.6 +/- 1.7 years. Quartiles of central PP (p < 0.001) predicted outcome more strongly than quartiles of brachial PP (p = 0.052). With adjustment for covariates, only the event rate in the fourth quartile of central PP (> or =50 mm Hg) was significantly higher than that in the first quartile (hazard ratio [HR]: 1.69, 95% confidence interval [CI]: 1.20 to 2.39, p = 0.003). Central PP > or =50 mm Hg was related to outcome in both men (HR: 2.06, 95% CI: 1.39 to 3.04, p < 0.001) and women (HR: 2.03, 95% CI: 1.55 to 2.65, p < 0.001); in participants with (HR: 1.84, 95% CI: 1.41 to 2.39, p < 0.001) and without diabetes (HR: 1.91, 95% CI: 1.29 to 2.83, p = 0.001); and in individuals younger (HR: 2.51, 95% CI: 1.59 to 3.95, p < 0.001) and older (HR: 1.53, 95% CI: 1.19 to 1.97, p = 0.001) than the age of 60 years. Central PP > or =50 mm Hg predicts adverse CVD outcome and may serve as a target in intervention strategies if confirmed in other populations and in prospective studies.
doi_str_mv 10.1016/j.jacc.2009.05.070
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We sought to determine a value that might predict adverse outcome and thereby provide a target for assessment of intervention strategies. We previously documented that central PP more strongly relates to carotid hypertrophy and extent of atherosclerosis and, more importantly, better predicts incident cardiovascular disease (CVD) than brachial PP. Radial applanation tonometry was performed in the third Strong Heart Study examination to determine central blood pressure. Cox regression analyses were performed using pre-specified covariates and quartiles of central and brachial PP. Among 2,405 participants without prevalent CVD, 344 suffered CVD events during 5.6 +/- 1.7 years. Quartiles of central PP (p &lt; 0.001) predicted outcome more strongly than quartiles of brachial PP (p = 0.052). With adjustment for covariates, only the event rate in the fourth quartile of central PP (&gt; or =50 mm Hg) was significantly higher than that in the first quartile (hazard ratio [HR]: 1.69, 95% confidence interval [CI]: 1.20 to 2.39, p = 0.003). Central PP &gt; or =50 mm Hg was related to outcome in both men (HR: 2.06, 95% CI: 1.39 to 3.04, p &lt; 0.001) and women (HR: 2.03, 95% CI: 1.55 to 2.65, p &lt; 0.001); in participants with (HR: 1.84, 95% CI: 1.41 to 2.39, p &lt; 0.001) and without diabetes (HR: 1.91, 95% CI: 1.29 to 2.83, p = 0.001); and in individuals younger (HR: 2.51, 95% CI: 1.59 to 3.95, p &lt; 0.001) and older (HR: 1.53, 95% CI: 1.19 to 1.97, p = 0.001) than the age of 60 years. 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With adjustment for covariates, only the event rate in the fourth quartile of central PP (&gt; or =50 mm Hg) was significantly higher than that in the first quartile (hazard ratio [HR]: 1.69, 95% confidence interval [CI]: 1.20 to 2.39, p = 0.003). Central PP &gt; or =50 mm Hg was related to outcome in both men (HR: 2.06, 95% CI: 1.39 to 3.04, p &lt; 0.001) and women (HR: 2.03, 95% CI: 1.55 to 2.65, p &lt; 0.001); in participants with (HR: 1.84, 95% CI: 1.41 to 2.39, p &lt; 0.001) and without diabetes (HR: 1.91, 95% CI: 1.29 to 2.83, p = 0.001); and in individuals younger (HR: 2.51, 95% CI: 1.59 to 3.95, p &lt; 0.001) and older (HR: 1.53, 95% CI: 1.19 to 1.97, p = 0.001) than the age of 60 years. 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We sought to determine a value that might predict adverse outcome and thereby provide a target for assessment of intervention strategies. We previously documented that central PP more strongly relates to carotid hypertrophy and extent of atherosclerosis and, more importantly, better predicts incident cardiovascular disease (CVD) than brachial PP. Radial applanation tonometry was performed in the third Strong Heart Study examination to determine central blood pressure. Cox regression analyses were performed using pre-specified covariates and quartiles of central and brachial PP. Among 2,405 participants without prevalent CVD, 344 suffered CVD events during 5.6 +/- 1.7 years. Quartiles of central PP (p &lt; 0.001) predicted outcome more strongly than quartiles of brachial PP (p = 0.052). With adjustment for covariates, only the event rate in the fourth quartile of central PP (&gt; or =50 mm Hg) was significantly higher than that in the first quartile (hazard ratio [HR]: 1.69, 95% confidence interval [CI]: 1.20 to 2.39, p = 0.003). Central PP &gt; or =50 mm Hg was related to outcome in both men (HR: 2.06, 95% CI: 1.39 to 3.04, p &lt; 0.001) and women (HR: 2.03, 95% CI: 1.55 to 2.65, p &lt; 0.001); in participants with (HR: 1.84, 95% CI: 1.41 to 2.39, p &lt; 0.001) and without diabetes (HR: 1.91, 95% CI: 1.29 to 2.83, p = 0.001); and in individuals younger (HR: 2.51, 95% CI: 1.59 to 3.95, p &lt; 0.001) and older (HR: 1.53, 95% CI: 1.19 to 1.97, p = 0.001) than the age of 60 years. Central PP &gt; or =50 mm Hg predicts adverse CVD outcome and may serve as a target in intervention strategies if confirmed in other populations and in prospective studies.</abstract><cop>New York, NY</cop><pub>Elsevier</pub><pmid>19850215</pmid><doi>10.1016/j.jacc.2009.05.070</doi><tpages>5</tpages></addata></record>
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subjects Aged
Aged, 80 and over
Biological and medical sciences
Blood Pressure - physiology
Body mass index
Brachial Artery - physiopathology
Cardiology
Cardiology. Vascular system
Cardiovascular disease
Cardiovascular Diseases - epidemiology
Cardiovascular Diseases - physiopathology
Cholesterol
Female
Follow-Up Studies
Heart attacks
Humans
Incidence
Male
Manometry
Medical sciences
Middle Aged
Mortality
Prevalence
Prognosis
Proportional Hazards Models
Retrospective Studies
Risk Factors
United States - epidemiology
title High Central Pulse Pressure Is Independently Associated With Adverse Cardiovascular Outcome: The Strong Heart Study
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