40 A protein biomarker model for detection of cardiac arrhythmia and prediction of associated heart failure

C. Tonry, K. McDonald, M. Ledwidge, B. Herandez, N. Glezeva, C. Rooney, B. Morrissey, S. Pennington, J. Baugh, Christopher A. Watson
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Abstract

Introduction Cardiac arrhythmia is strongly linked with heart failure (HF) and a primary cause of stroke. The condition affects around 37,000 people in Northern Ireland although it is estimated that many thousands more remain undiagnosed. It is important to be able to diagnose cardiac arrhythmia early, so that appropriate interventions can be made to reduce risk of subsequent stroke or HF. Currently, diagnosis and management of cardiac arrhythmia is reliant on assessment of clinical risk factors, however, routine monitoring of circulating biomarkers would significantly improve accuracy for prediction of arrhythmia and associated adverse events. The aim of this study was to (i) identify protein biomarkers, which can predict cardiac arrhythmia and (ii) identify protein biomarkers that are predictive of HF in patients with arrhythmia. Methods Multiple Reaction Monitoring mass spectrometry-based assays were developed for measurement of a selection of candidate protein biomarkers of cardiovascular injury. Assays were developed using nanoflow reverse phase C18 chromatographic ChipCube based separation, coupled to an Agilent 6460 triple quadrupole mass spectrometer. Optimised MRM assays were applied, in a sample blinded manner, for analysis of a cohort of 410 serum samples. This included 112 patients with cardiac arrhythmia as well as matched controls without cardiac arrhythmia. Results MRM assays were established for measurement of 25 proteins. Individually, a number of the biomarker proteins show significant differential expression between patients with and without cardiac arrhythmia. An 11-protein biomarker model was identified, which was comparable to BNP in prediction of HF within the cardiac arrhythmia subset of patients (Protein panel AUC = 0.856 vs BNP AUC = 0.838). Combination of the 11 proteins with BNP notably enhanced the predictive capacity of BNP (AUC = 0.898). Conclusions/Implications Through this study, assays have been developed for robust, multiplexed measurement of 25 cardiovascular disease-associated proteins in patient serum samples. A number of proteins were identified, which show significant expression changes in association with cardiac arrhythmia and will be further explored. Importantly, a statistical model revealed a panel of 11 proteins, which can predict HF in patients with cardiac arrhythmia, with comparable accuracy to BNP. This panel will need to be further validated in independent patient cohorts.
一种检测心律失常和预测相关心力衰竭的蛋白质生物标志物模型
心律失常与心力衰竭(HF)密切相关,是中风的主要原因。这种情况影响了北爱尔兰约37,000人,尽管据估计还有数千人未被诊断出来。能够早期诊断心律失常是很重要的,这样可以采取适当的干预措施来降低随后中风或心衰的风险。目前,心律失常的诊断和治疗依赖于临床危险因素的评估,然而,常规监测循环生物标志物将显著提高心律失常和相关不良事件预测的准确性。本研究的目的是:(1)鉴定可预测心律失常的蛋白质生物标志物,(2)鉴定可预测心律失常患者心衰的蛋白质生物标志物。方法建立了基于多反应监测质谱的检测方法,用于测量心血管损伤的候选蛋白质生物标志物。采用基于ChipCube的纳米流反相C18色谱分离,与Agilent 6460三重四极杆质谱联用。以样本盲法对410份血清样本进行了优化的MRM分析。这包括112例心律失常患者以及匹配的无心律失常对照。结果建立了25种蛋白的MRM检测方法。个别而言,许多生物标志物蛋白在有和没有心律失常的患者中表现出显著的表达差异。鉴定出一种11蛋白生物标志物模型,该模型在预测心律失常亚群患者HF方面与BNP相当(蛋白质面板AUC = 0.856 vs BNP AUC = 0.838)。11种蛋白联合BNP可显著提高BNP的预测能力(AUC = 0.898)。结论/意义通过这项研究,已经开发出了对患者血清样本中25种心血管疾病相关蛋白进行稳健、多路测量的检测方法。我们发现了一些与心律失常相关的蛋白,这些蛋白的表达发生了显著变化,我们将对这些蛋白进行进一步的研究。重要的是,一个统计模型揭示了一组11种蛋白质,可以预测心律失常患者的HF,其准确性与BNP相当。该小组将需要在独立患者队列中进一步验证。
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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