心衰患者早期主动脉瓣疾病发展的预后意义:来自MECKI评分队列的见解

European heart journal open Pub Date : 2025-06-06 eCollection Date: 2025-05-01 DOI:10.1093/ehjopen/oeaf066
Veronika A Myasoedova, Elisabetta Salvioni, Alice Bonomi, Arianna Galotta, Massimo Mapelli, Irene Mattavelli, Valentina Rusconi, Francesca Bertolini, Jeness Campodonico, Mauro C Contini, Ilaria Massaiu, Vincenza Valerio, Paolo Poggio, Piergiuseppe Agostoni
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引用次数: 0

摘要

目的:心力衰竭(HF)仍然是一个主要的临床挑战,因此识别高危HF患者对于改善患者护理、优化资源分配和简化医疗流程至关重要。在各种风险模型中,代谢运动试验数据结合心脏和肾脏指标评分是心衰预后的重要预测指标。然而,主动脉瓣硬化(AV)这一新兴的心血管疾病标志物与心衰预后之间的关系目前研究甚少。方法和结果:我们评估了1397例HF患者(2006-2019),经胸超声心动图发现房颤硬化。评估全因死亡率和心血管综合结局。统计分析采用Kaplan-Meier曲线和Cox回归模型。时间依赖性分析用于评价房颤硬化在心衰患者中的作用。基线时,707例患者出现房室硬化(50.6%)。房颤硬化患者年龄更大,心衰更严重。5年后,基线时的房室硬化与全因死亡率增加有关(HR = 1.4, 95% CI: 1.1-1.8;P = 0.005)和心血管结局(HR = 1.4, 95% CI: 1.0-2.0;P = 0.044),但对两组间所有变量进行校正后,差异无统计学意义。基线时无房室硬化患者的进一步超声心动图评估显示,40%的病例中观察到房室硬化的发展与全因死亡率密切相关(HR = 3.4, 95% CI: 1.3-10.8;P = 0.017)和心血管结局(HR = 6.0, 95% CI: 1.3-26.9;P = 0.02)。结论:在HF中,房室硬化是HF严重程度的标志,其发展应被视为疾病进展的标志,而不是不良预后的独立预后因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Prognostic significance of early stage aortic valve disease development in heart failure: insights from the MECKI score cohort.

Prognostic significance of early stage aortic valve disease development in heart failure: insights from the MECKI score cohort.

Prognostic significance of early stage aortic valve disease development in heart failure: insights from the MECKI score cohort.

Prognostic significance of early stage aortic valve disease development in heart failure: insights from the MECKI score cohort.

Aims: Heart failure (HF) continues to pose a major clinical challenge, making the identification of high-risk HF patients crucial for improving patient care, optimizing resource allocation, and streamlining healthcare processes. Among various risk models, the metabolic exercise test data combined with cardiac and kidney indexes score stands out as a strong predictor of HF prognosis. However, the relationship between aortic valve (AV) sclerosis, an emerging marker of cardiovascular disease, and HF prognosis are currently poorly studied.

Methods and results: We evaluated 1397 HF patients (2006-2019) and AV sclerosis was identified by transthoracic echocardiography. All-cause mortality and composite cardiovascular outcomes were assessed. Statistical analyses included Kaplan-Meier curves and Cox regression models. Time-dependent analyses were conducted to evaluate the role of AV sclerosis development in HF patients. At baseline, 707 patients presented AV sclerosis (50.6%). Patients with AV sclerosis were older and had more severe HF. After 5 years, AV sclerosis at baseline was linked to increased all-cause mortality (HR = 1.4, 95% CI: 1.1-1.8; P = 0.005) and cardiovascular outcomes (HR = 1.4, 95% CI: 1.0-2.0; P = 0.044) but, after adjustment for all variables different between the two groups, significance was lost. Further echocardiographic evaluation of patients without AV sclerosis at baseline reveals that AV sclerosis development, observed in >40% of cases, was strongly associated with all-cause mortality (HR = 3.4, 95% CI: 1.3-10.8; P = 0.017) and cardiovascular outcomes (HR = 6.0, 95% CI: 1.3-26.9; P = 0.02).

Conclusion: In HF, AV sclerosis is a marker of HF severity and its development should be considered a marker of disease progression rather than an independent prognostic factor for poor outcomes.

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