Startseite Comparison of the cardiac troponin I-cardiac troponin T-troponin C complex and cardiac troponin I and T in distinguishing myocardial infarction using a single sample at presentation
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Comparison of the cardiac troponin I-cardiac troponin T-troponin C complex and cardiac troponin I and T in distinguishing myocardial infarction using a single sample at presentation

  • Ling Li , Yuqing Liu , Yu Wu , Juan Yang , Litao Zhang ORCID logo , Xin Shu , Hui Wang , Yisha Jing , Tongxin Ni , Liyao Gou , Yi Zhang EMAIL logo und Zhenlu Zhang EMAIL logo
Veröffentlicht/Copyright: 11. November 2025
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Abstract

Objectives

The potential relationship between cardiac troponin (cTn) composition and etiologies of myocardial injury may provide diagnostic insights for myocardial infarction (MI). We compared the performance of novel ternary cTnI–cTnT–TnC complex (ITC) assays with high-sensitivity (hs)-cTnI and hs-cTnT in differentiating MI patients at presentation.

Methods

Plasma samples from 1,210 patients with suspected MI were collected. Major cTn forms were quantified using long-cTnT ITC complex, hs-total ITC complex, hs-cTnI and hs-cTnT assay. We compared the assay performance based on the 99th percentile upper reference limits (URLs), evaluated their area under the receiver operating characteristic curve (AUC), and assessed their ability to differentiate MI using established cut-off values.

Results

A total of 138 (11.4 %) patients were diagnosed with MI. 86 % patients had long-cTnT ITC complex concentration below the 99th percentile URLs (sensitivity: 0.818, specificity: 0.943, NPV: 0.975, PPV: 0.649). AUC was 0.959 for long-cTnT ITC complex, comparable to hs-cTnI (0.953) and superior to hs-total ITC complex (0.889) and hs-cTnT (0.927). Using established cut-off values, the long-cTnT ITC complex assay classified 10 % of patients as rule-in and 52 % as rule-out (sensitivity: 0.993, NPV: 0.998, specificity: 0.972, PPV: 0.760), which was comparable to hs-cTnI and better than hs-total ITC complex and hs-cTnT. In early-presenting patients, the long-cTnT ITC complex demonstrated enhanced discrimination and improved diagnostic performance.

Conclusions

The long-cTnT ITC complex assay demonstrated performance comparable to hs-cTnI and superior to hs-total ITC complex and hs-cTnT in distinguishing MI using a single sample at presentation. These findings suggest its potential utility in improving risk stratification and triage strategies, particularly among early-presenting patients.


Corresponding authors: Yi Zhang, Immunoassay Reagent R&D Department, Shenzhen Mindray Bio-Medical Electronics Co., Ltd, Shenzhen, 518000, China, E-mail: ; and Zhenlu Zhang, Clinical Laboratory of Wuhan Asia Heart Hospital, No.753 Jinghan Avenue, Wuhan, 430022, Wuhan, Hubei, China, E-mail:
Ling Li and Yuqing Liu contributed equally to this work.

Funding source: Noncommunicable Chronic Diseases-National Science and Technology Major Project

Award Identifier / Grant number: 2023ZD0509500

  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. Zhenlu Zhang and Yi Zhang contributed to the conception and design of the study. Ling Li and Yuqing Liu contributed to acquisition, analysis, interpretation of data and the manuscript drafting. Yu Wu, Juan Yang, Litao Zhang, Xin Shu, Hui Wang, Yisha Jing, Tongxin Ni and Liyao Gou contributed to manuscript check and modification.

  4. Use of Large Language Models, AI and Machine Learning Tools: None declared.

  5. Conflict of interest: Shenzhen Mindray Bio-Medical Electronics Co., Ltd. has filed for the patent applications PCT/CN2023/112993, PCT/ CN2023/112994, and PCT/CN2024/112205.

  6. Research funding: This study was supported by Noncommunicable Chronic Diseases-National Science and Technology Major Project (2023ZD0509500) and Shenzhen Mindray Bio-Medical Electronics Co., Ltd. Financial support was not dependent on the results of the study.

  7. Data availability: On appropriate request.

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Supplementary Material

This article contains supplementary material (https://doi.org/10.1515/cclm-2025-0385).


Received: 2025-03-27
Accepted: 2025-09-05
Published Online: 2025-11-11

© 2025 Walter de Gruyter GmbH, Berlin/Boston

Heruntergeladen am 14.11.2025 von https://www.degruyterbrill.com/document/doi/10.1515/cclm-2025-0385/pdf?lang=de
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