超声心动图右心室舒张末期基底直径指数对结缔组织病伴肺动脉高压的预后价值

IF 2.4 4区 医学 Q2 RHEUMATOLOGY International Journal of Rheumatic Diseases Pub Date : 2025-01-10 DOI:10.1111/1756-185X.70061
Wu Qianwen, Ye Huangshu, Ma Hong, Gan Xiaoxia, Zhang Ning, Gu Lei, Zhu Yinsu, Zhou Lei, Zhou Yanli, Zhang Miaojia, Sun Xiaoxuan, Wang Qiang
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引用次数: 0

摘要

背景:右心室(RV)衰竭是肺动脉高压(PAH)不良结局的一个公认的关键预后因素,而右心室扩张对适应性或非适应性改变具有重要意义。多环芳烃是结缔组织病(CTD)患者死亡的主要原因。本研究旨在阐明超声心动图(ECHO)评估的左心室形态学在CTD合并PAH (CTD-PAH)中的预后意义。方法:在这项双视角队列研究中,纳入2013年至2023年通过右侧心导管(RHC)诊断的143例CTD-PAH患者。记录临床特点、实验室资料、超声心动图参数(右心室舒张末期基底直径指数(RVDDI)、三尖瓣环面收缩偏移(TAPSE)、肺动脉收缩压(PASP))及治疗情况。主要终点被定义为5年内的临床恶化。分析方法包括Kaplan-Meier生存分析、log-rank检验和多变量Cox比例风险回归来评估预后因素。结果:该研究共纳入143例CTD-PAH患者,女性占明显优势(95.1%),中位年龄为41.67岁;SLE-PAH(49%)和pSS-PAH(34%)是最常见的亚型,94%的参与者属于WHO-FC II-III型。在参与者中,34例(23.8%)患者在21个月的中位随访期间出现临床恶化。在校正了年龄和性别等混杂因素后,由ECHO测定的RVDDI与临床恶化相关(HR 1.090;95% ci: 1.019-1.166;p = 0.012)。RVDDI bbb25.81 mm/m2预测CTD-PAH患者临床恶化的发生率较高。在TAPSE/PASP > 0.19 mm/mmHg亚组中,RVDDI > 25.81 mm/m2的患者临床恶化的发生率更高。估计1年和3年无事件生存率分别为93.5%和53.7%。结论:本研究表明,通过ECHO评估的RVDDI是CTD-PAH临床恶化的重要预后指标。将其纳入RV功能评估和风险分层可能为CTD-PAH人群提供有价值的增量预后信息。
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The Prognostic Value of Right Ventricular End-Diastolic Basal Diameter Index by Echocardiography in Connective Tissue Diseases Associated With Pulmonary Artery Hypertension

Background

Right ventricular (RV) failure is a well-recognized pivotal prognostic factor of adverse outcomes in pulmonary artery hypertension (PAH), while RV dilation provides significant implications for adaptive or maladaptive changes. PAH is a predominant cause of mortality among patients with connective tissue disease (CTD). This study aims to elucidate the prognostic significance of RV morphology, as assessed by echocardiography (ECHO), in with CTD associated with PAH (CTD-PAH).

Methods

In this ambispective cohort study, 143 CTD-PAH patients diagnosed by right-sided heart catheterization (RHC) from 2013 to 2023 were enrolled. Clinical characteristics, laboratory data, echocardiographic parameters (right ventricular end-diastolic basal diameter index (RVDDI), tricuspid annular plane systolic excursion (TAPSE) and pulmonary arterial systolic pressure (PASP)) and therapy were recorded. The primary endpoint was defined as clinical worsening within a five-year timeframe. Analytical methods included Kaplan–Meier survival analyses, the log-rank test, and multivariable Cox proportional hazards regression to evaluate prognostic factors.

Results

The study enrolled a total of 143 patients with CTD-PAH, with a notable female predominance (95.1%) and a median age of 41.67 years; SLE-PAH (49%) and pSS-PAH (34%) were the most common subtypes, and 94% of the participants were in WHO-FC II-III. Among the participants, 34 (23.8%) patients experienced clinical worsening during a median follow-up period of 21 months. After adjusting for confounders such as age and sex, RVDDI, as determined by ECHO was correlated with clinical worsening (HR 1.090; 95% CI: 1.019–1.166; p = 0.012). RVDDI > 25.81 mm/m2 predicts higher incidence of clinical worsening in CTD-PAH. In the subgroup of TAPSE/PASP > 0.19 mm/mmHg, patients with RVDDI > 25.81 mm/m2 had a higher incidence of clinical worsening. The estimated event-free survival rates at 1 and 3 years were 93.5% and 53.7%, respectively.

Conclusion

The study demonstrates that RVDDI, as evaluated by ECHO, is a significant prognostic indicator for clinical worsening in CTD-PAH. Its inclusion in the assessment of RV function and risk stratification may provide valuable incremental prognostic information for this CTD-PAH population.

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来源期刊
CiteScore
3.70
自引率
4.00%
发文量
362
审稿时长
1 months
期刊介绍: The International Journal of Rheumatic Diseases (formerly APLAR Journal of Rheumatology) is the official journal of the Asia Pacific League of Associations for Rheumatology. The Journal accepts original articles on clinical or experimental research pertinent to the rheumatic diseases, work on connective tissue diseases and other immune and allergic disorders. The acceptance criteria for all papers are the quality and originality of the research and its significance to our readership. Except where otherwise stated, manuscripts are peer reviewed by two anonymous reviewers and the Editor.
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