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抗高血压药物类别对心血管结局的影响:STEP研究的见解

Impact of antihypertensive drug classes on cardiovascular outcomes: insights from the STEP study.

作者信息

Peng Xinyi, Olsen Michael Hecht, Pareek Manan, Bai Jingjing, Liu Yang, Song Qirui, Cai Jun

机构信息

State Key Laboratory of Cardiovascular Disease of China, National Center for Cardiovascular Diseases of China, Hypertension Center, Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beilishi Rd. 167, Xicheng District , Beijing, 100037, China.

Beijing Institute of Heart, Lung and Blood Vessel Diseases, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.

出版信息

BMC Med. 2025 Jul 1;23(1):365. doi: 10.1186/s12916-025-04158-z.

Abstract

BACKGROUND

The optimal class of antihypertensive drugs for reducing cardiovascular risk remains unclear. This study investigated whether prolonged exposure to specific antihypertensive drug classes is associated with lower cardiovascular risk in individuals with well-controlled blood pressure.

METHODS

This study utilised data from the STEP trial, which enrolled elderly, hypertensive Chinese patients with no history of stroke. After excluding 234 patients lost to follow-up and 20 patients without blood pressure records after randomisation, 8257 patients were included. The relative time on each antihypertensive drug (medication time/event time) was calculated. The primary outcome was a composite of the first occurrence of stroke, acute coronary syndrome (ACS), acute decompensated heart failure, coronary revascularisation, atrial fibrillation, and cardiovascular death. Secondary endpoints included individual components of the primary outcome. Cox regression analysis was used to estimate hazard ratios (HRs) with 95% confidence intervals (CIs) for each outcome.

RESULTS

Over a median 3.34 years follow-up, primary outcome analysis revealed that longer relative exposure to angiotensin II receptor blockers (ARBs) or calcium channel blockers (CCBs) significantly reduced cardiovascular risk. Each unit increase in relative time on ARBs was associated with a 45% lower risk of the primary outcome (HR 0.55, 95% CI 0.43-0.70), whereas CCBs reduced risk by 30% (HR 0.70, 95% CI 0.54-0.92). Diuretics demonstrated neutral results. Conversely, longer relative time on beta-blockers was linked to a higher primary outcome risk (HR 2.20, 95% CI 1.81-2.68). Regarding secondary outcomes, extended exposure to both ARBs and CCBs was significantly associated with lower risks of all-cause and cardiovascular mortality. Longer exposure to ARBs produced additional benefits by reducing risks of stroke, ACS, and major adverse cardiac events (MACE). The HRs for ARBs per-unit increase in relative time remained consistently lower than those of CCBs across the primary outcome, MACE, and stroke (all P < 0.05).

CONCLUSIONS

This post hoc analysis suggested that ARBs and CCBs might be more favourable for composite cardiovascular outcomes than diuretics and beta-blockers. ARBs appeared to offer greater cardiovascular benefits than CCBs. Longer exposure to beta-blockers was associated with a higher cardiovascular risk, which might reflect a selection bias based on medical indications.

TRIAL REGISTRATION

STEP ClinicalTrials.gov number, NCT03015311. Registered 2 January 2017.

摘要

背景

降低心血管风险的最佳抗高血压药物类别仍不明确。本研究调查了长期暴露于特定抗高血压药物类别是否与血压控制良好的个体心血管风险降低相关。

方法

本研究利用了STEP试验的数据,该试验纳入了无中风病史的老年高血压中国患者。在排除234例失访患者和20例随机分组后无血压记录的患者后,纳入了8257例患者。计算每种抗高血压药物的相对使用时间(用药时间/事件时间)。主要结局是首次发生中风、急性冠状动脉综合征(ACS)、急性失代偿性心力衰竭、冠状动脉血运重建、心房颤动和心血管死亡的复合事件。次要终点包括主要结局的各个组成部分。使用Cox回归分析估计每个结局的风险比(HRs)及95%置信区间(CIs)。

结果

在中位3.34年的随访中,主要结局分析显示,较长时间相对暴露于血管紧张素II受体阻滞剂(ARB)或钙通道阻滞剂(CCB)可显著降低心血管风险。ARB相对时间每增加一个单位,主要结局风险降低45%(HR 0.55,95%CI 0.43 - 0.70),而CCB可使风险降低30%(HR 0.70,95%CI 0.54 - 0.92)。利尿剂显示出中性结果。相反,β受体阻滞剂相对时间较长与较高的主要结局风险相关(HR 2.20,95%CI 1.81 - 2.68)。关于次要结局,较长时间暴露于ARB和CCB均与全因死亡率和心血管死亡率较低显著相关。较长时间暴露于ARB通过降低中风、ACS和主要不良心脏事件(MACE)的风险产生了额外益处。在主要结局、MACE和中风方面,ARB相对时间每增加一个单位的HR始终低于CCB(所有P < 0.05)。

结论

这项事后分析表明,对于复合心血管结局,ARB和CCB可能比利尿剂和β受体阻滞剂更有利。ARB似乎比CCB提供更大的心血管益处。较长时间暴露于β受体阻滞剂与较高的心血管风险相关,这可能反映了基于医学指征的选择偏倚。

试验注册

STEP,ClinicalTrials.gov编号,NCT03015311。2017年1月2日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af44/12219695/649d8711a891/12916_2025_4158_Fig1_HTML.jpg

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