Evidence map›Paper›PMID 42125242›Full record

ArticleJournal of inflammation research2026

High-Sensitivity Troponin I and NT-proBNP as Early Indicators of Disease Severity and Prognostic Markers in Immune Checkpoint Inhibitor-Associated Fulminant Myocarditis.

Chongmei Zhou, Qiong Ma

Abstract read
In one paragraph

Article in Journal of inflammation research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Chongmei ZhouDepartment of Clinical Laboratory, Henan Provincial People's Hospital, Zhengzhou University People's Hospital, Henan University People's Hospital, Zhengzhou, Henan Province, 450003, People's Republic of China.
Qiong MaDepartment of Clinical Laboratory, Henan Provincial People's Hospital, Zhengzhou University People's Hospital, Henan University People's Hospital, Zhengzhou, Henan Province, 450003, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The study aims to investigate the utility of high-sensitivity cardiac troponin I (hs-cTnI) and N-terminal pro-brain natriuretic peptide (NT-proBNP) measured at initial presentation as indicators of disease severity and prognostic markers in patients with immune checkpoint inhibitor (ICI)-associated myocarditis. While these biomarkers reflect myocardial injury and ventricular dysfunction-consequences of the underlying pathology-their levels at diagnosis may aid in early risk stratification and identification of patients likely to follow a fulminant course. Methods: This study implemented a retrospective cohort design, involving 341 patients identified with myocarditis associated with immune checkpoint inhibitors (ICIs). The participants were divided into two categories: those with fulminant myocarditis (62 subjects) and those with non-fulminant myocarditis (279 subjects). An in-depth examination was conducted on their clinical features, biomarker concentrations, and health outcomes. To ascertain the predictive capability of these biomarkers, multivariable logistic regression analyses and survival assessments were utilized. Additionally, a subgroup analysis was carried out by classifying patients into high and low biomarker groups according to the optimal cutoff points determined through receiver operating characteristic (ROC) curve evaluations. The subgroups were then compared regarding treatment modalities (including immunosuppressive therapy and mechanical circulatory support) and clinical outcomes (including ICU admission, complications, and survival). Results: Patients with fulminant myocarditis had significantly higher hs-cTnI (1.38 ± 0.56 vs. 0.22 ± 0.10ng/mL) and NT-proBNP (2384.43 ± 912.67 vs. 528.72 ± 192.33pg/mL) levels (both Conclusion: Hs-cTnI and NT-proBNP levels at presentation are strong indicators of myocardial injury severity and ventricular dysfunction in ICI-associated myocarditis. Their measurement facilitates early risk stratification, identifying patients at highest risk for fulminant disease who may benefit from intensive monitoring and timely intervention. Additionally, pre-existing cardiovascular comorbidities remain crucial for identifying vulnerable populations prior to ICI initiation.

Indexed as

high-sensitivity cardiac troponin Iimmune checkpoint inhibitorsN-terminal pro-brain natriuretic peptideprognostic biomarkersrisk stratificationtumor treatment-related fulminant myocarditis

Identifiers

PMID42125242
PMCPMC13159950

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.