收缩压低于 130 mmHg 可降低超声心动图左心室肥厚型高血压患者的心血管事件发生率

IF 3.1 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Maria Lembo, Valentina Trimarco, Raffaele Izzo, Maria Virginia Manzi, Francesco Rozza, Paola Gallo, Carmine Morisco, Luca Bardi, Giovanni Esposito, Imma Forzano, Gaetano Santulli, Bruno Trimarco
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引用次数: 0

摘要

背景:最近的报告表明,心电图左心室肥厚(ECG-LVH)达到收缩压(SBP)的高血压患者死亡率增加 方法:为了填补这一长期知识空白,我们对 9511 名高血压患者进行了为期 33.6 [IQR 7.9-72.7] 个月的随访:为了填补这一长期存在的知识空白,我们对 9511 名高血压患者进行了为期 33.6 [IQR 7.9-72.7] 个月的随访。根据随访期间达到的平均 SBP({小于或等于}130、130-139 和 {大于或等于}140mmHg)以及无/有回声-LVH 将患者分为六组。主要终点是致命性或非致命性心肌梗死和中风、心脏性猝死、需要住院治疗的心力衰竭、血管重建和颈动脉支架植入术的复合终点。次要终点包括心房颤动和短暂性脑缺血发作。研究结果在随访期间,Echo-LVH 患者和未接受 Echo-LVH 治疗的患者达到的 SBP 和舒张压(DBP)相当。引人注目的是,回声-LVH 和 SBP>130mmHg 患者的主要和次要终点发生率明显更高,SBP{大于或等于}140mmHg 的回声-LVH 组发生率最高。在调整了潜在的混杂因素后,通过单独的 Cox 多变量回归,主要终点和次要终点均与 SBP{ 大于或等于}140mmHg 和 Echo-LVH 显著相关。相反,DBP 下降{小于或等于}80mmHg 与继发性事件发生率的显著增加有关。结论:对于患有 Echo-LVH 的高血压患者,实现治疗中平均 SBP 目标值{小于或等于}130mmHg 对心血管事件的发生率具有有利的预后影响。意义声明 与最近的报道相反,实现治疗期间 SBP≤130mmHg 可降低回声-LVH 高血压患者的心血管事件发生率。降低 DBP≤80mmHg 反而与较高的冠心病并发症发生率相关。通过 Cox 多变量回归模型,调整潜在的混杂因素,硬性和软性 CV 事件的发生率与 Echo-LVH 和 SBP≥140mmHg 显著相关。我们的数据表明,回声-LVH 患者的治疗策略应以降低 SBP≤130mmHg 为目标,同时注意不要降低 DBP≤80mmHg。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Achieving a Systolic Blood Pressure Below 130 mmHg Reduces the Incidence of Cardiovascular Events in Hypertensive Patients with Echocardiographic Left Ventricular Hypertrophy.

Background: Recent reports have evidenced an increased mortality rate in hypertensive patients with electrocardiographic left ventricular hypertrophy (ECG-LVH) achieving systolic blood pressure (SBP) <130 mmHg. However, to the best of our knowledge, the actual effects of blood pressure reduction to the ≤130/80 mmHg target on the incidence of cardiovascular (CV) events have never been determined in hypertensive patients with a diagnosis of left ventricular hypertrophy based on echocardiographic criteria (Echo-LVH). Methods: To fill this long-standing knowledge gap, we harnessed a population of 9511 hypertensive patients, followed-up for 33.6 [interquartile range 7.9-72.7] months. The population was divided into six groups according to the average SBP achieved during the follow-up (≤130, 130-139, and ≥140 mmHg) and absence/presence of Echo-LVH. The primary endpoint was a composite of fatal or nonfatal myocardial infarction and stroke, sudden cardiac death, heart failure requiring hospitalization, revascularization, and carotid stenting. Secondary endpoints included atrial fibrillation and transient ischemic attack. Results: During the follow-up, achieved SBP and diastolic blood pressure (DBP) were comparable between patients with and without Echo-LVH. Strikingly, the rates of primary and secondary endpoints were significantly higher in patients with Echo-LVH and SBP >130 mmHg, reaching the highest values in the Echo-LVH group with SBP ≥140 mmHg. By separate Cox multivariable regressions, after adjusting for potential confounders, both primary and secondary endpoints were significantly associated with SBP ≥140 mmHg and Echo-LVH. Instead, DBP reduction ≤80 mmHg was associated with a significant increased rate of secondary events. Conclusions: In hypertensive patients with Echo-LVH, achieving an average in-treatment SBP target ≤130 mmHg has a beneficial prognostic impact on incidence of CV events. SIGNIFICANCE STATEMENT: Contrary to recent findings, achieving in-treatment SBP ≤130 mmHg lowers the incidence of CV events in hypertensive patients with Echo-LVH. However, reducing DBP ≤80 mmHg is linked to increased CV complications. Cox multivariable regression models, considering potential confounders, reveal that the rate of hard and soft CV events is significantly associated with Echo-LVH and SBP ≥140 mmHg. Our data indicate that therapeutic strategies for Echo-LVH patients should target SBP ≤130 mmHg while avoiding lowering DBP ≤80 mmHg.

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来源期刊
CiteScore
6.90
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0.00%
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115
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1 months
期刊介绍: A leading research journal in the field of pharmacology published since 1909, JPET provides broad coverage of all aspects of the interactions of chemicals with biological systems, including autonomic, behavioral, cardiovascular, cellular, clinical, developmental, gastrointestinal, immuno-, neuro-, pulmonary, and renal pharmacology, as well as analgesics, drug abuse, metabolism and disposition, chemotherapy, and toxicology.
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