Practical approaches to the detection of macrotroponin.

IF 2.1 4区 医学 Q3 MEDICAL LABORATORY TECHNOLOGY
Annals of Clinical Biochemistry Pub Date : 2024-03-01 Epub Date: 2023-09-02 DOI:10.1177/00045632231197301
Leo Lam, Campbell Kyle
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引用次数: 0

Abstract

Introduction: Macrotroponin is increasingly recognised as a cause of confusion in interpreting high-sensitivity cardiac troponin (hs-cTnI) results. In this study, we sought to evaluate two practical approaches to detecting macrotroponin. These two approaches are PEG precipitation and SVM (support vector machine) analysis to classify discrepancies between hs-cTn assays.

Method: Residual serum and heparin plasma specimens (n = 483) with initially elevated hs-cTnI from hospital and community laboratories were retested on multiple hs-cTn platforms before and after PEG precipitation and Protein A immunoglobulin depletion. SVM analysis was conducted to identify a linear equation that best discriminated specimens with macrotroponin using a combination of results from two different hs-cTn assays.

Findings: The diagnostic performance of PEG precipitation was carried out using Protein A immunoglobulin depletion as the reference comparator. When a cutoff residual activity after PEG precipitation of ≤ 20% was used, this threshold carried a high specificity of 92% (confidence interval 83-98%; n = 189) using the Siemens hs-cTnI Vista assay and 95% specificity (86%-98%; n = 242) using the Abbott hs-cTnI Architect assay. SVM analysis generated a linear equation identifying macrotroponin specimens from results obtained on two hs-cTn assays. This approach can be highly specific, comparable to PEG precipitation when certain assay combinations and concentrations are used.

Conclusion: We describe and identify practical alternatives to detecting macrotroponin. These approaches can be optimised for high specificity, reducing the need for more complex laboratory methods.

检测大促红细胞生成素的实用方法。
导言:大肌钙蛋白越来越被认为是解释高敏心肌肌钙蛋白(hs-cTnI)结果时容易混淆的一个原因。在本研究中,我们试图评估两种检测大肌钙蛋白的实用方法。这两种方法是 PEG 沉淀法和 SVM(支持向量机)分析法,用于对 hs-cTn 检测之间的差异进行分类:方法:对医院和社区实验室最初出现 hs-cTnI 升高的残留血清和肝素血浆标本(n = 483)在 PEG 沉淀和蛋白 A 免疫球蛋白去除前后在多个 hs-cTn 平台上进行复检。通过 SVM 分析,结合两种不同的 hs-cTn 检测方法的结果,确定了最能鉴别大促红细胞生成素标本的线性方程:以蛋白 A 免疫球蛋白耗竭为参照对比,对 PEG 沉淀的诊断性能进行了研究。当使用 PEG 沉淀后残留活性≤20% 的临界值时,使用西门子 hs-cTnI Vista 检测法,该临界值的特异性高达 92%(置信区间 83-98%;n = 189);使用雅培 hs-cTnI Architect 检测法,该临界值的特异性高达 95%(置信区间 86-98%;n = 242)。SVM 分析法根据两种 hs-cTn 检测法得出的结果生成了一个线性方程来确定大促红细胞生成素标本。这种方法具有很高的特异性,在使用特定的检测组合和浓度时可与 PEG 沉淀法相媲美:我们描述并确定了检测大促红细胞生成素的实用替代方法。结论:我们描述并确定了检测大促红细胞生成素的实用替代方法,这些方法可优化为高特异性,从而减少对更复杂实验室方法的需求。
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来源期刊
Annals of Clinical Biochemistry
Annals of Clinical Biochemistry Biochemistry, Genetics and Molecular Biology-Clinical Biochemistry
CiteScore
5.20
自引率
4.50%
发文量
61
期刊介绍: Annals of Clinical Biochemistry is the fully peer reviewed international journal of the Association for Clinical Biochemistry and Laboratory Medicine. Annals of Clinical Biochemistry accepts papers that contribute to knowledge in all fields of laboratory medicine, especially those pertaining to the understanding, diagnosis and treatment of human disease. It publishes papers on clinical biochemistry, clinical audit, metabolic medicine, immunology, genetics, biotechnology, haematology, microbiology, computing and management where they have both biochemical and clinical relevance. Papers describing evaluation or implementation of commercial reagent kits or the performance of new analysers require substantial original information. Unless of exceptional interest and novelty, studies dealing with the redox status in various diseases are not generally considered within the journal''s scope. Studies documenting the association of single nucleotide polymorphisms (SNPs) with particular phenotypes will not normally be considered, given the greater strength of genome wide association studies (GWAS). Research undertaken in non-human animals will not be considered for publication in the Annals. Annals of Clinical Biochemistry is also the official journal of NVKC (de Nederlandse Vereniging voor Klinische Chemie) and JSCC (Japan Society of Clinical Chemistry).
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