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SPRINT 试验符合条件的 ACCORD-BP 参与者强化与标准血压控制的比较。

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

机构信息

Department of Pharmacotherapy and Outcomes Science, Virginia Commonwealth University, Richmond, VA.

Department of Pharmacy Practice, School of Pharmacy, University of Connecticut, Storrs, CT.

出版信息

Diabetes Care. 2017 Dec;40(12):1733-1738. doi: 10.2337/dc17-1366. Epub 2017 Sep 25.

DOI:10.2337/dc17-1366
PMID:28947569
Abstract

OBJECTIVE

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).

RESEARCH DESIGN AND METHODS

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.

RESULTS

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).

CONCLUSIONS

Intensive BP control reduced CVD outcomes in a cohort of participants with T2DM and additional CVD risk factors.

摘要

目的

我们旨在确定强化血压(BP)控制对 2 型糖尿病(T2DM)和心血管疾病(CVD)额外风险因素患者心血管结局的影响。

研究设计和方法

这是 ACCORD-BP(糖尿病血压控制行动以降低心血管风险)参与者的事后、多变量、亚组分析。如果参与者符合 ACCORD-BP 的标准血糖控制组,并且还具有 SPRINT(收缩压干预试验)资格所需的额外 CVD 风险因素,则有资格进行分析。我们使用 Cox 比例风险回归模型来比较强化与标准 BP 控制对 CVD 结局的影响。将“SPRINT 合格”的 ACCORD-BP 参与者与 SPRINT 参与者进行汇总,以确定强化 BP 控制的效果是否与 T2DM 相互作用。

结果

强化和标准 BP 控制组的基线Framingham 10 年 CVD 风险评分分别为 14.5%和 14.8%。强化和标准 BP 控制组的平均达到收缩压值分别为 120 和 134mmHg(<0.001)。强化 BP 控制降低了 CVD 死亡、非致死性心肌梗死(MI)、非致死性卒中和任何血运重建以及心力衰竭的复合终点(风险比 0.79;95%CI 0.65-0.96;P=0.02)。强化 BP 控制还降低了 CVD 死亡、非致死性 MI 和非致死性卒中(风险比 0.69;95%CI 0.51-0.93;P=0.01)。接受强化 BP 控制的参与者更频繁地发生治疗相关不良事件(4.1% vs. 2.1%;P=0.003)。强化 BP 控制对 CVD 结局的影响在有和没有 T2DM 的患者之间没有差异(>0.62)。

结论

强化 BP 控制降低了 T2DM 和额外 CVD 风险因素患者的 CVD 结局。

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