涉及多个部位的高血压介导的器官损伤是心血管事件的独立风险因素。

European heart journal open Pub Date : 2023-10-04 eCollection Date: 2023-09-01 DOI:10.1093/ehjopen/oead102
Maria Lembo, Daniela Pacella, Maria Virginia Manzi, Carmine Morisco, Lucia La Mura, Costantino Mancusi, Luca Bardi, Valentina Trimarco, Bruno Trimarco, Raffaele Izzo, Giovanni Esposito
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摘要

目的:慢性压力超负荷决定了功能和结构的改变,导致高血压介导的器官损伤(HMOD),影响多个地区。我们的目的是评估一个或多个部位HMOD的缺失与存在以及高血压患者的血压(BP)和代谢控制对预后的影响。方法和结果:该研究包括来自坎帕尼亚致敬网络注册中心的7237名高血压患者,随访5.3±4.5年。作为HMOD,我们分析了左心室肥大、颈动脉斑块和慢性肾脏疾病(CKD-EPI≥3期)的存在,并评估了HMOD的零位点与一位点与二位点与三位点对主要心血管不良事件(MACE)发生的影响。还考虑了血压控制和胰岛素抵抗代谢评分(METS-IR)。57.3%的患者实现了最佳血压控制。351名(4.8%)患者发生了主要心血管不良事件。没有HMOD的患者的MACE率为2.7%,而有一个、两个和三个HMOD位点的患者的MAC率分别为4.7%、7.9%和9.8%。通过使用Cox多变量模型,经年龄、血压控制、平均心率、平均METS-IR、HMOD位点数量和药物调整后,发现MACE与衰老、平均METS-IR、抗血小板治疗和HMOD的多个位点显著相关,而与肾素-血管紧张素系统抑制剂药物呈负相关。结论:在高血压患者中,尽管代谢失调有显著影响,但MACE的风险随着HMOD涉及的地区数量的增加而增加,与血压控制无关。涉及多个部位的高血压介导的器官损伤是高血压和代谢障碍的有害后果,但一旦确定,它代表了MACE发生的独立心血管风险因素。
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Hypertension-mediated organ damage involving multiple sites is an independent risk factor for cardiovascular events.

Aims: Chronic pressure overload determines functional and structural alterations, leading to hypertension-mediated organ damage (HMOD), affecting multiple districts. We aim at evaluating the prognostic impact of the absence vs. presence of HMOD in one or more sites and of blood pressure (BP) and metabolic control in hypertensive patients.

Methods and results: The study included 7237 hypertensive patients from the Campania Salute Network Registry, followed up for 5.3 ± 4.5 years. As HMOD, we analysed the presence of left ventricular hypertrophy, carotid plaques, and chronic kidney disease (CKD-EPI ≥3 stage) and evaluated the impact of zero vs. one vs. two vs. three sites of HMOD on the occurrence of major adverse cardiovascular events (MACEs). Blood pressure control and Metabolic Score for Insulin Resistance (METS-IR) were also considered. Optimal BP control was achieved in 57.3% patients. Major adverse cardiovascular events occurred in 351 (4.8%) patients. The MACE rate in patients without HMOD was 2.7%, whereas it was 4.7, 7.9, and 9.8% in patients with one, two, and three sites with HMOD, respectively. By using Cox multivariate models, adjusted for age, BP control, mean heart rate, mean METS-IR, number of HMOD sites, and drugs, MACE was found to be significantly associated with ageing, mean METS-IR, anti-platelet therapy, and multiple sites with HMOD, whereas a negative association was found with renin-angiotensin system inhibitor drugs.

Conclusion: In hypertensive patients, the risk of MACE increases with the incremental number of districts involved by HMOD, independent of BP control and despite the significant impact of metabolic dysregulation. Hypertension-mediated organ damage involving multiple sites is the deleterious consequence of hypertension and dysmetabolism but, when established, it represents an independent cardiovascular risk factor for MACE occurrence.

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