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轻链淀粉样变的预后:通过心内膜心肌活检证实心脏受累的患者的生存预测的多变量分析。

Prognosis of light chain amyloidosis: a multivariable analysis for survival prediction in patients with cardiac involvement proven by endomyocardial biopsy.

机构信息

Department of Internal Medicine III, Cardiology, Angiology and Pneumology, University Hospital Heidelberg, Heidelberg, Germany.

Institute of Medical Biometry, University of Heidelberg, Heidelberg, Germany.

出版信息

Open Heart. 2023 Jul;10(2). doi: 10.1136/openhrt-2023-002310.

Abstract

BACKGROUND

Cardiac involvement is a main determinant of mortality in light chain (AL) amyloidosis but data on survival of patients with cardiac AL amyloidosis proven by endomyocardial biopsy (EMB) are sparse.

METHODS

This study analysed clinical, laboratory, electrocardiography and echocardiographic parameters for their prognostic value in the assessment of patients with AL amyloidosis and cardiac involvement. Patients with AL amyloidosis who had their first visit to the amyloidosis centre at the University Hospital Heidelberg between 2006 and 2017 (n=1628) were filtered for cardiac involvement proven by EMB. In the final cohort, mortality-associated markers were analysed by univariate and multivariable Cox regression. Cut-off values for each parameter were calculated using the survival time.

RESULTS

One-hundred and seventy-four patients could be identified. Median overall survival time was 1.5 years and median follow-up time was 5.2 years. At the end of the investigation period, 115 patients had died. In multivariable analysis, New York Heart Association-functional class >II (HR 1.65; 95% CI 1.09 to 2.50; p=0.019), left ventricular global longitudinal strain (HR 1.12; 95% CI 1.03 to 1.22; p=0.007), left ventricular end-systolic volume (HR 1.02; 95% CI 1.01 to 1.03; p=0.001), systolic pulmonary artery pressure (HR 0.98; 95% CI 0.96 to 0.99; p=0.027), N-terminal pro-B-type natriuretic peptide (HR 1.57; 95% CI 1.17 to 2.11; p=0.003) and difference in free light chains (HR 1.30; 95% CI 1.05 to 1.62; p=0.017) were independently predictive.

CONCLUSION

Among all patients with AL amyloidosis those with cardiac involvement represent a high-risk population with limited therapy options. Therefore, accurate risk stratification is necessary to identify cardiac amyloidosis patients with favourable prognosis. Incorporation of modern imaging techniques into existing or newly developed scoring systems is a promising option that might enable the implementation of risk-adapted therapeutic strategies.

摘要

背景

心脏受累是轻链(AL)淀粉样变患者死亡的主要决定因素,但通过心内膜心肌活检(EMB)证实的心脏 AL 淀粉样变患者的生存数据很少。

方法

本研究分析了临床、实验室、心电图和超声心动图参数,以评估 AL 淀粉样变合并心脏受累患者的预后价值。2006 年至 2017 年间,在海德堡大学医院淀粉样变性中心首次就诊的 AL 淀粉样变患者(n=1628)中筛选出通过 EMB 证实有心脏受累的患者。在最终队列中,通过单变量和多变量 Cox 回归分析与死亡率相关的标志物。使用生存时间计算每个参数的截止值。

结果

共确定了 174 名患者。中位总生存时间为 1.5 年,中位随访时间为 5.2 年。在研究结束时,115 名患者死亡。多变量分析中,纽约心脏协会功能分级>II 级(HR 1.65;95%CI 1.09 至 2.50;p=0.019)、左心室整体纵向应变(HR 1.12;95%CI 1.03 至 1.22;p=0.007)、左心室收缩末期容积(HR 1.02;95%CI 1.01 至 1.03;p=0.001)、收缩期肺动脉压(HR 0.98;95%CI 0.96 至 0.99;p=0.027)、N 末端脑利钠肽前体(HR 1.57;95%CI 1.17 至 2.11;p=0.003)和游离轻链差值(HR 1.30;95%CI 1.05 至 1.62;p=0.017)是独立的预测因素。

结论

在所有 AL 淀粉样变患者中,合并心脏受累的患者是一个高危人群,治疗选择有限。因此,需要进行准确的风险分层,以识别预后良好的心脏淀粉样变患者。将现代影像学技术纳入现有的或新开发的评分系统是一种很有前途的选择,这可能使风险适应性治疗策略的实施成为可能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10c2/10357742/cda11070b39c/openhrt-2023-002310f01.jpg

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