高敏感性心肌肌钙蛋白I对野生型转甲状腺素淀粉样心肌病的危险分层。

IF 8.4 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Circulation: Heart Failure Pub Date : 2025-08-01 Epub Date: 2025-05-15 DOI:10.1161/CIRCHEARTFAILURE.125.012816
Laura De Michieli, Giulio Sinigiani, Gianluigi Guida, Giulia Saturi, Giuseppe Sena, Teresa Maria Capovilla, Anna Cantone, Alessandro Cianca, Alessandro Lupi, Aldostefano Porcari, Giacomo Tini, Giuseppe Vergaro, Francesco Cappelli, Riccardo Albertini, Matteo Bianco, Roberta Mussinelli, Matteo Serenelli, Beatrice Musumeci, Stefano Perlini, Marco Merlo, Simone Longhi, Gianfranco Sinagra, Martina Perazzolo Marra, Sabino Iliceto, Allan S Jaffe, Giovanni Palladini, Alberto Cipriani, Paolo Milani
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引用次数: 0

摘要

背景:在野生型转甲状腺蛋白淀粉样蛋白心肌病中,用hs-cTnI(高敏感性心肌肌钙蛋白I)定义预后的阈值尚未得到系统的解决,部分原因是hs-cTnI检测的多样性。本研究的目的是,首先,评估不同检测方法在野生型转甲状腺蛋白淀粉样心肌病患者中测量的hs-cTnI的预后表现,其次,确定检测特异性的hs-cTnI预后阈值,该阈值可整合到风险分层分期系统中。方法:采用Abbott Architect Stat hs-cTnI检测、Beckman Coulter Access hs-cTnI检测(检测队列)和Siemens Centaur XPT hs-cTnI检测(验证队列),对来自不同队列的稳定型野生型转甲状腺素淀粉样蛋白心肌病患者进行多中心观察性研究。结果是全因死亡率。结果:在Abbott队列中(n=136;中位随访22[13-41]个月;31例[23%]死亡)和Beckman队列(n=98;中位随访19[12-28]个月;16例[16%]死亡),自然对数转换hs-cTnI是死亡率的独立预测因子(调整年龄和性别的风险比为1.62 [95% CI, 1.11-2.35];P=0.012和2.47 [95% CI, 1.48-4.14];P80 ng/L)和NPs(利钠肽,NT-proBNP [n -末端前b型NP] >3000 ng/L或BNP (b型利钠肽)>250 ng/L)鉴定出3组预后逐渐恶化。然后将分期系统(使用hs-cTnI >80 ng/L和NT-proBNP>3000 ng/L)应用于使用hs-cTnI Siemens assay评估的独立队列(n=345,中位随访32(24-42)个月,119例(34%)死亡)。各组间的显著差异保持不变。结论:在野生型转甲状腺蛋白淀粉样心肌病患者中,hs-cTnI是一个强有力且独立的死亡率预测因子。这3项检测的hs-cTnI阈值为80 ng/L,可单独和在NP分期系统中提供有效的风险分层。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
High-Sensitivity Cardiac Troponin I for Risk Stratification in Wild-Type Transthyretin Amyloid Cardiomyopathy.

Background: Thresholds to define prognosis with hs-cTnI (high-sensitivity cardiac troponin I) have not been systematically addressed in wild-type transthyretin amyloid cardiomyopathy, in part because of the multiplicity of hs-cTnI assays. The aims of this study were: first, to assess the prognostic performance of hs-cTnI measured with different assays in patients with wild-type transthyretin amyloid cardiomyopathy and, second, to identify assay-specific hs-cTnI thresholds for prognosis that could be integrated into staging systems for risk stratification.

Methods: Observational multicenter study of stable wild-type transthyretin amyloid cardiomyopathy patients from different cohorts using the Abbott Architect Stat hs-cTnI assay and the Beckman Coulter Access hs-cTnI assay (testing cohorts) and the Siemens Centaur XPT hs-cTnI assay (validation cohort). Outcome was all-cause mortality.

Results: In the Abbott cohort (n=136; median follow-up 22 [13-41] months; 31 [23%] deaths) and Beckman cohort (n=98; median follow-up 19 [12-28] months; 16 [16%] deaths), natural log-transformed hs-cTnI was an independent predictor of mortality (age- and sex-adjusted hazard ratio, 1.62 [95% CI, 1.11-2.35]; P=0.012 and 2.47 [95% CI, 1.48-4.14]; P<0.001, respectively). The best hs-cTnI threshold for 18-month mortality of the combined Abbott/Beckman cohorts (n=234) was 81 ng/L, rounded to 80 ng/L for simplicity of clinical use. A 2-variable staging system (based on the Mayo Clinic system) using hs-cTnI (>80 ng/L) and NPs (natriuretic peptides; NT-proBNP [N-terminal pro-B-type natriuretic peptide] >3000 ng/L or BNP [B-type natriuretic peptide] >250 ng/L) identified 3 groups with progressively worse prognosis. The staging system (using hs-cTnI >80 ng/L and NT-proBNP>3000 ng/L) was then applied to an independent cohort evaluated with the hs-cTnI Siemens assay (n=345, median follow-up 32 [24-42] months, 119 [34%] deaths). The significant differences between the groups were maintained.

Conclusions: In patients with wild-type transthyretin amyloid cardiomyopathy, hs-cTnI is a strong and independent predictor of mortality. A threshold of hs-cTnI of 80 ng/L for these 3 assays provides effective risk stratification alone and in a staging system with NP.

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来源期刊
Circulation: Heart Failure
Circulation: Heart Failure 医学-心血管系统
CiteScore
12.90
自引率
3.10%
发文量
271
审稿时长
6-12 weeks
期刊介绍: Circulation: Heart Failure focuses on content related to heart failure, mechanical circulatory support, and heart transplant science and medicine. It considers studies conducted in humans or analyses of human data, as well as preclinical studies with direct clinical correlation or relevance. While primarily a clinical journal, it may publish novel basic and preclinical studies that significantly advance the field of heart failure.
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