高灵敏度肌钙蛋白检测法布里病心肌病的应用

IF 1.8 Q2 Biochemistry, Genetics and Molecular Biology
JIMD reports Pub Date : 2025-08-12 DOI:10.1002/jmd2.70008
Subadra Wanninayake, Tejas Kalaria, Antonio Ochoa-Ferraro, Ashwin Roy, Richard Steeds, Tarekegn Geberhiwot, Charlotte Dawson
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引用次数: 0

摘要

法布里病(FD)是一种x连锁溶酶体积存病,导致溶酶体在多个器官中积累鞘糖脂。在本研究中,我们(1)比较了高敏感性心肌肌钙蛋白I和T (hs-cTnI和hs-cTnT)作为Fabry心肌病(FC)的标志物,(2)评估了hs-cTn在监测早期FC中的作用,以确定是否存在一个阈值,可以可靠地排除显著FC。数据回顾性收集来自英国伯明翰遗传代谢紊乱服务中心的成年FD患者的临床记录。包括心脏磁共振成像并同时进行hs-cTnT和/或hs-cTnI测量的患者。FC定义为LVH和/或晚期钆增强和低T1 /伪正常的心脏磁共振成像特征。133例患者(男性54例)(hs-cTn发生率259例),62例有显著FC, 71例无FC。hs-cTnI和hs-cTnT通过分数比表达进行比较(FRTn=hs-cTn浓度/年龄和性别特异性的第99百分位数)。在有和没有心肌病的患者中,FRTnI和FRTnT的分布没有差异(中位数[四分位数间距],0.89[0.52-2.02]对1.02 [0.47-1.9],p = 0.270)。在区分有无FC患者时,hs-cTn的曲线下面积(AUC)较高(AUC = 0.974;95% ci: 0.959-0.990;p < 0.001),高于FRTn (AUC = 0.897)和NT-proBNP (AUC = 0.939)。排除FC的最佳阈值为hs-cTn <; 8.5 ng/L(敏感性97.8%,阴性预测值97.2%),在该阈值下hs-cTnT和hs-cTnI的性能相当。血清hs-cTn升高程度与心脏受累程度相关。我们得出结论,连续hs-cTn监测优于NTproBNP监测早期FC。cMRI扫描可以识别FC的特征,这些特征是开始治疗的指标,可以优先考虑hs-cTn >; 8.5 ng/L的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The Utility of High-Sensitivity Troponin to Detect Cardiomyopathy in Patients With Fabry Disease

The Utility of High-Sensitivity Troponin to Detect Cardiomyopathy in Patients With Fabry Disease

Fabry disease (FD) is an X-linked lysosomal storage disease resulting in lysosomal accumulation of glycosphingolipids in multiple organs. In this study, we (1) compare high-sensitivity cardiac troponins I and T (hs-cTnI and hs-cTnT) as markers of Fabry cardiomyopathy (FC), and (2) evaluate the role of hs-cTn in monitoring early-stage FC to establish if there is a threshold at which significant FC can be reliably excluded. Data were collected retrospectively from clinical records of adults with FD seen in the Inherited Metabolic Disorders service, Birmingham, UK. Patients with cardiac magnetic resonance imaging and concurrent hs-cTnT and/or hs-cTnI measurement(s) were included. FC was defined as the cardiac magnetic resonance imaging features of LVH and/or late gadolinium enhancement and low/pseudonormal T1. One hundred thirty-three patients (male = 54) were included (hs-cTn incidences = 259), 62 patients had significant FC, and 71 did not have FC. hs-cTnI and hs-cTnT were compared by expressing as the fractional ratio (FRTn=hs-cTn concentration/age- and sex-specific 99th percentile). The distribution of FRTnI and FRTnT was not different (median [interquartile range], 0.89 [0.52–2.02] vs. 1.02 [0.47–1.9], p = 0.270), including in patients with and without cardiomyopathy. In differentiating patients with FC from those without, the area under the curve (AUC) for hs-cTn was higher (AUC = 0.974; 95% CI: 0.959–0.990; p < 0.001) than for FRTn (AUC = 0.897) and NT-proBNP (AUC = 0.939). A threshold hs-cTn < 8.5 ng/L was optimal to exclude FC (sensitivity 97.8% and negative predictive value 97.2%) with comparable performance of hs-cTnT and hs-cTnI at this threshold. The degree of serum hs-cTn elevation correlated with the severity of cardiac involvement. We conclude that serial hs-cTn monitoring is superior to NTproBNP for monitoring for early FC. cMRI scans to identify features of FC that are indicators to start treatment can be prioritised to patients with hs-cTn > 8.5 ng/L.

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来源期刊
JIMD reports
JIMD reports Biochemistry, Genetics and Molecular Biology-Biochemistry, Genetics and Molecular Biology (miscellaneous)
CiteScore
3.30
自引率
0.00%
发文量
84
审稿时长
12 weeks
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