Hemodynamic Comparison And Prognostication Of V122I Versus Wild Type Transthyretin Amyloid Cardiomyopathy

IF 8.2 2区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS Journal of Cardiac Failure Pub Date : 2025-01-01 Epub Date: 2025-01-14 DOI:10.1016/j.cardfail.2024.10.036
Joban Vaishnav , Lisa R Yanek , Bairavi Shankar , Artrish Jefferson , Yazan Alshawkan , Daniel Tsottles , Serena Zampino , Godoy Lola , Vivek Jani , Mark Ranek , Michael Polydefkis , Kavita Sharma
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Abstract

Introduction

Transthyretin amyloid cardiomyopathy (ATTR-CM), in particular V122I disease, is a highly morbid cause of heart failure (HF). There are limited contemporary data on hemodynamic prognostication in ATTR-CM. We aimed to compare hemodynamics and evaluate prognostic significance in patients with V122I and wild type (wt) ATTR-CM.

Hypothesis

We hypothesize that patients with V122I will have more hemodynamic abnormalities and that hemodynamics will have additive prognostic value in ATTR-CM.

Methods

Patients with either V122I or wtATTR-CM who underwent RHC at our center were included. Hemodynamic abnormalities by each group and prognostic relevance by classic cut offs with endpoint of death was assessed. Characteristics for V122I or wtATTR-CM were compared using chi-squared or Fisher's exact tests, or t-tests or Wilcoxon tests. Kaplan-Meier curves and Cox proportional hazard regression models were used to assess relationships with mortality and the composite of mortality or HF hospitalization.

Results

Of 152 patients, 73 (48%) had V122I variant. V122I vs wtATTR patients were younger (72.7 [7.4] v 78.5 [7.3] yrs), more likely Black (94.5 v 17.7%), and NHYA Class III or IV (53.8 v 35.1%), all p<0.05, with no significant difference in National Amyloid Center (NAC) staging. On RHC, V122I patients were more likely to have abnormal filling pressures compared to wtATTR including mRA >8 (61.1% v 43.8%), mPAP >25 (75.0% v 54.8%), PCWP >18 (56.9% v 38.4%), all p<0.05. CI was low in the majority of patients and not different by V122I v wtATTR (CI <2.2: 82.6% v 80.3%, p=0.72, CI <1.8: 56.5% v 53.5%, p=0.72). V122I patients with abnormal mPAP, PCWP, and CI had significantly lower survival when compared to V122I patients with normal parameters and wtATTR patients with normal and abnormal parameters (Figure). Hemodynamics independently predicted risk on top of NAC stage 3 disease (p<0.05 for all parameters, Table).

Conclusion

The majority of patients with ATTR-CM have abnormal hemodynamics, with greater derangement in V122I disease. In patients with abnormal hemodynamics, V122I patients had poorer survival compared to wtATTR. Hemodynamics are independently predictive of adverse outcomes on top of classification in the most severe prognostic stage. In the era of non-invasive diagnosis for ATTR-CM, our findings highlight the ongoing role for hemodynamic investigation in patients with ATTR-CM.
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V122I型与野生型转甲状腺素淀粉样心肌病的血流动力学比较及预后
转甲状腺素淀粉样心肌病(atr - cm),特别是V122I疾病,是心力衰竭(HF)的高度病态原因。目前关于atr - cm的血流动力学预测数据有限。我们的目的是比较V122I型和野生型(wt) atr - cm患者的血流动力学并评估其预后意义。假设我们假设V122I患者会有更多的血流动力学异常,并且血流动力学对atr - cm有附加的预后价值。方法纳入在本中心行RHC的V122I或wattr - cm患者。评估各组的血流动力学异常情况以及与死亡终点的经典截断线的预后相关性。使用卡方检验或Fisher精确检验、t检验或Wilcoxon检验比较V122I或wattr - cm的特征。Kaplan-Meier曲线和Cox比例风险回归模型用于评估与死亡率的关系以及死亡率或HF住院的复合。结果152例患者中,73例(48%)有V122I变异。V122I与wtATTR患者更年轻(72.7 [7.4]vs 78.5[7.3]岁),更可能是Black (94.5 v 17.7%), NHYA III或IV级(53.8 v 35.1%),均为p<;0.05,在国家淀粉样蛋白中心(NAC)分期上无显著差异。在RHC上,V122I患者比wtATTR患者更容易出现异常充盈压力,包括mRA >;8 (61.1% vs 43.8%), mPAP >25 (75.0% vs 54.8%), PCWP >18 (56.9% vs 38.4%),均为p<;0.05。大多数患者CI较低,V122I v wtATTR差异无统计学意义(CI <2.2: 82.6% v 80.3%, p=0.72; CI <1.8: 56.5% v 53.5%, p=0.72)。mPAP、PCWP和CI异常的V122I患者与参数正常的V122I患者和参数正常和异常的wtATTR患者相比,生存率明显降低(图)。血流动力学独立预测NAC 3期疾病的风险(p<0.05,所有参数,表)。结论绝大多数atr - cm患者血流动力学异常,以V122I病变更为严重。在血液动力学异常的患者中,与wtATTR相比,V122I患者的生存期较差。在最严重的预后阶段,血流动力学可独立预测分类上的不良后果。在无创诊断atr - cm的时代,我们的研究结果强调了血流动力学研究在atr - cm患者中的持续作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Cardiac Failure
Journal of Cardiac Failure 医学-心血管系统
CiteScore
7.80
自引率
8.30%
发文量
653
审稿时长
21 days
期刊介绍: Journal of Cardiac Failure publishes original, peer-reviewed communications of scientific excellence and review articles on clinical research, basic human studies, animal studies, and bench research with potential clinical applications to heart failure - pathogenesis, etiology, epidemiology, pathophysiological mechanisms, assessment, prevention, and treatment.
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