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Licensed Unlicensed Requires Authentication Published by De Gruyter September 26, 2023

Evaluation of the analytical and clinical performance of a new high-sensitivity cardiac troponin I assay: hs-cTnI (CLIA) assay

  • Ling Li , Xin Shu , Litao Zhang ORCID logo , Ao Xu , Juan Yang , Yisha Jing , Hui Wang and Zhenlu Zhang EMAIL logo

Abstract

Objectives

Cardiac troponin (cTn) is the key biomarker for diagnosis of acute coronary syndrome (ACS). We performed a complete assessment of the high-sensitivity cardiac troponin I (hs-cTnI) (CLIA) assay on the analytical performance and clinical diagnostic performance, which was compared with Abbott ARCHITECT hs-cTnI assay.

Methods

Sex-specific 99th percentile upper reference limits (URLs) were determined from a healthy population of 424 males and 408 females. High-sensitivity performance was assessed by examining the imprecision at sex-specific URLs and the detectable results above LoD in a cohort of healthy population. The diagnostic performance of the hs-cTnI (CLIA) assay was validated in a population of 934 patients with suspected ACS.

Results

The 99th percentile URLs were 15.3 ng/L for female, 31.3 ng/L for male and 24.2 ng/L for overall population. The total imprecision near the sex-specific 99th percentile URLs were <5 %. 76.74 % of females, 97.12 % of males and 86.69 % of overall population had cTnI values exceeding the LoD, which met the criteria of high-sensitivity troponin assay. No cross-reactivity or interference was identified. The diagnostic sensitivity, specificity, PPV, NPV, and AUC of hs-cTnI (CLIA) assay were 97.97 , 90.70, 79.02, 99.21 % and 0.9885, respectively, which were comparable to ARCHITECT hs-cTnI assay.

Conclusions

hs-cTnI (CLIA) assay is a high-sensitivity troponin I method with high precision, sensitivity and specificity. The clinical diagnostic performance of hs-cTnI (CLIA) is comparable to the established ARCHITECT hs-cTnI assay. Mindray’s hs-cTnI (CLIA) assay is an attractive alternative for diagnosis of myocardial infarction with a high level of accuracy and safety.


Corresponding author: Dr. Zhenlu Zhang, Clinical Laboratory of Wuhan Asia Heart Hospital, 432000, Wuhan, Hubei, P.R. China, E-mail:
Ling Li and Xin Shu contributed equally to this work.

Funding source: Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

  1. Research ethics: The present study carried out at Wuhan Asia Heart hospital (Wuhan, Hubei province, China) was approved by the Ethics Committee in accordance with the Helsinki Declaration.

  2. Informed consent: Not applicable.

  3. Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  4. Competing interests: The authors declare that there is no conflict of interest.

  5. Research funding: This project was supported by Shenzhen Mindray Bio-Medical Electronics Co., Ltd. for financial support. Financial support was not dependent on the results of the study.

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Supplementary Material

This article contains supplementary material (https://doi.org/10.1515/cclm-2023-0529).


Received: 2023-05-19
Accepted: 2023-08-25
Published Online: 2023-09-26
Published in Print: 2024-01-26

© 2023 Walter de Gruyter GmbH, Berlin/Boston

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