Intensive Versus Standard Blood Pressure Control in SPRINT-Eligible Participants of ACCORD-BP

We sought to determine the effect of intensive blood pressure (BP) control on cardiovascular outcomes in participants with type 2 diabetes mellitus (T2DM) and additional risk factors for cardiovascular disease (CVD). This study was a post hoc, multivariate, subgroup analysis of ACCORD-BP (Action to...

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Veröffentlicht in:Diabetes care 2017-12, Vol.40 (12), p.1733-1738
Hauptverfasser: Buckley, Leo F, Dixon, Dave L, Wohlford, 4th, George F, Wijesinghe, Dayanjan S, Baker, William L, Van Tassell, Benjamin W
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container_end_page 1738
container_issue 12
container_start_page 1733
container_title Diabetes care
container_volume 40
creator Buckley, Leo F
Dixon, Dave L
Wohlford, 4th, George F
Wijesinghe, Dayanjan S
Baker, William L
Van Tassell, Benjamin W
description We sought to determine the effect of intensive blood pressure (BP) control on cardiovascular outcomes in participants with type 2 diabetes mellitus (T2DM) and additional risk factors for cardiovascular disease (CVD). This study was a post hoc, multivariate, subgroup analysis of ACCORD-BP (Action to Control Cardiovascular Risk in Diabetes Blood Pressure) participants. Participants were eligible for the analysis if they were in the standard glucose control arm of ACCORD-BP and also had the additional CVD risk factors required for SPRINT (Systolic Blood Pressure Intervention Trial) eligibility. We used a Cox proportional hazards regression model to compare the effect of intensive versus standard BP control on CVD outcomes. The "SPRINT-eligible" ACCORD-BP participants were pooled with SPRINT participants to determine whether the effects of intensive BP control interacted with T2DM. The mean baseline Framingham 10-year CVD risk scores were 14.5% and 14.8%, respectively, in the intensive and standard BP control groups. The mean achieved systolic BP values were 120 and 134 mmHg in the intensive and standard BP control groups ( < 0.001). Intensive BP control reduced the composite of CVD death, nonfatal myocardial infarction (MI), nonfatal stroke, any revascularization, and heart failure (hazard ratio 0.79; 95% CI 0.65-0.96; = 0.02). Intensive BP control also reduced CVD death, nonfatal MI, and nonfatal stroke (hazard ratio 0.69; 95% CI 0.51-0.93; = 0.01). Treatment-related adverse events occurred more frequently in participants receiving intensive BP control (4.1% vs. 2.1%; = 0.003). The effect of intensive BP control on CVD outcomes did not differ between patients with and without T2DM ( > 0.62). Intensive BP control reduced CVD outcomes in a cohort of participants with T2DM and additional CVD risk factors.
doi_str_mv 10.2337/dc17-1366
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This study was a post hoc, multivariate, subgroup analysis of ACCORD-BP (Action to Control Cardiovascular Risk in Diabetes Blood Pressure) participants. Participants were eligible for the analysis if they were in the standard glucose control arm of ACCORD-BP and also had the additional CVD risk factors required for SPRINT (Systolic Blood Pressure Intervention Trial) eligibility. We used a Cox proportional hazards regression model to compare the effect of intensive versus standard BP control on CVD outcomes. The "SPRINT-eligible" ACCORD-BP participants were pooled with SPRINT participants to determine whether the effects of intensive BP control interacted with T2DM. The mean baseline Framingham 10-year CVD risk scores were 14.5% and 14.8%, respectively, in the intensive and standard BP control groups. The mean achieved systolic BP values were 120 and 134 mmHg in the intensive and standard BP control groups ( &lt; 0.001). Intensive BP control reduced the composite of CVD death, nonfatal myocardial infarction (MI), nonfatal stroke, any revascularization, and heart failure (hazard ratio 0.79; 95% CI 0.65-0.96; = 0.02). Intensive BP control also reduced CVD death, nonfatal MI, and nonfatal stroke (hazard ratio 0.69; 95% CI 0.51-0.93; = 0.01). Treatment-related adverse events occurred more frequently in participants receiving intensive BP control (4.1% vs. 2.1%; = 0.003). The effect of intensive BP control on CVD outcomes did not differ between patients with and without T2DM ( &gt; 0.62). 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Intensive BP control reduced the composite of CVD death, nonfatal myocardial infarction (MI), nonfatal stroke, any revascularization, and heart failure (hazard ratio 0.79; 95% CI 0.65-0.96; = 0.02). Intensive BP control also reduced CVD death, nonfatal MI, and nonfatal stroke (hazard ratio 0.69; 95% CI 0.51-0.93; = 0.01). Treatment-related adverse events occurred more frequently in participants receiving intensive BP control (4.1% vs. 2.1%; = 0.003). The effect of intensive BP control on CVD outcomes did not differ between patients with and without T2DM ( &gt; 0.62). 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This study was a post hoc, multivariate, subgroup analysis of ACCORD-BP (Action to Control Cardiovascular Risk in Diabetes Blood Pressure) participants. Participants were eligible for the analysis if they were in the standard glucose control arm of ACCORD-BP and also had the additional CVD risk factors required for SPRINT (Systolic Blood Pressure Intervention Trial) eligibility. We used a Cox proportional hazards regression model to compare the effect of intensive versus standard BP control on CVD outcomes. The "SPRINT-eligible" ACCORD-BP participants were pooled with SPRINT participants to determine whether the effects of intensive BP control interacted with T2DM. The mean baseline Framingham 10-year CVD risk scores were 14.5% and 14.8%, respectively, in the intensive and standard BP control groups. The mean achieved systolic BP values were 120 and 134 mmHg in the intensive and standard BP control groups ( &lt; 0.001). Intensive BP control reduced the composite of CVD death, nonfatal myocardial infarction (MI), nonfatal stroke, any revascularization, and heart failure (hazard ratio 0.79; 95% CI 0.65-0.96; = 0.02). Intensive BP control also reduced CVD death, nonfatal MI, and nonfatal stroke (hazard ratio 0.69; 95% CI 0.51-0.93; = 0.01). Treatment-related adverse events occurred more frequently in participants receiving intensive BP control (4.1% vs. 2.1%; = 0.003). The effect of intensive BP control on CVD outcomes did not differ between patients with and without T2DM ( &gt; 0.62). Intensive BP control reduced CVD outcomes in a cohort of participants with T2DM and additional CVD risk factors.</abstract><cop>United States</cop><pub>American Diabetes Association</pub><pmid>28947569</pmid><doi>10.2337/dc17-1366</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0003-0688-4487</orcidid><oa>free_for_read</oa></addata></record>
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subjects Aged
Antihypertensive Agents - therapeutic use
Blood pressure
Blood Pressure - drug effects
Cardiovascular disease
Cardiovascular diseases
Cardiovascular system
Cerebral infarction
Diabetes
Diabetes mellitus
Diabetes Mellitus, Type 2 - complications
Diabetes Mellitus, Type 2 - mortality
Female
Hazards
Health hazards
Health risks
Heart diseases
Heart Failure - etiology
Heart Failure - mortality
Heart Failure - prevention & control
Humans
Hypertension - drug therapy
Hypertension - mortality
Male
Middle Aged
Myocardial infarction
Myocardial Infarction - etiology
Myocardial Infarction - mortality
Myocardial Infarction - prevention & control
Pressure effects
Proportional Hazards Models
Regression analysis
Regression models
Research design
Risk analysis
Risk Factors
Risk management
Stroke - etiology
Stroke - mortality
Stroke - prevention & control
Treatment Outcome
title Intensive Versus Standard Blood Pressure Control in SPRINT-Eligible Participants of ACCORD-BP
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