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NOD 样受体含 pyrin 结构域 3 炎性小体诱导的细胞焦亡对儿童病毒性心肌炎的影响

 

Authors Huang H, Lou J, Chen W, Cheng X, Xing X, Huang S 

Received 16 June 2025

Accepted for publication 2 November 2025

Published 15 November 2025 Volume 2025:18 Pages 7003—7011

DOI https://doi.org/10.2147/IJGM.S547439

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 3

Editor who approved publication: Prof. Dr. Yuriy Sirenko

Huang Huang,1 Jiwen Lou,2 Wenhao Chen,2 Xiangyi Cheng,2 Xinchan Xing,3 Shen Huang4 

1Science of Prescription, Academy of Chinese Medicine, Henan University of Chinese Medicine, Zhengzhou, Henan, People’s Republic of China; 2Pediatrics of Chinese Medicine, School of Pediatric Medicine, Henan University of Chinese Medicine, Zhengzhou, Henan, People’s Republic of China; 3Department of Pediatrics, Zhengzhou Second Middle School Hospital, Zhengzhou, Henan, People’s Republic of China; 4Department of Pediatrics, The First Affiliated Hospital of Henan University of Chinese Medicine, Zhengzhou, Henan, People’s Republic of China

Correspondence: Shen Huang, Department of Pediatrics, The First Affiliated Hospital of Henan University of Chinese Medicine, Zhengzhou, Henan, People’s Republic of China, Tel +86-017600350021, Email huangshenfahhucm@uic-edu.cn

Purpose: Viral myocarditis (VMC) is a leading cause of heart failure and dilated cardiomyopathy in children. Pyroptosis, an inflammatory form of programmed cell death mediated by NOD-like receptor pyrin domain-containing 3 (NLRP3) inflammasomes, has been implicated in myocardial injury. However, the diagnostic significance of combined gene and protein expression analysis remains unclear. This study aimed to clarify the role of NLRP3 inflammasome-mediated pyroptosis in pediatric VMC and assess whether integrated gene–protein profiling could enhance diagnostic prediction.
Patients and Methods: A total of 100 children were enrolled, including a case group (n=50, children with viral myocarditis hospitalized between September 2023 and September 2024) and a control group (n=50, patients with dilated cardiomyopathy during the same time period). The expression levels of proteins interleukin-1β (IL-1β), NLRP3, Gasdermin D (GSDMD) and Caspase-1, and genes GSDMD, NLRP3, and Caspase-1 in myocardial tissues were measured through enzyme-linked immunosorbent assay, immunohistochemistry, real-time polymerase chain reaction, and Western blotting.
Results: No significant differences were found between the two groups regarding age, gender, or clinical history (P> 0.05). Compared with the control group, the case group exhibited significantly higher expression of NLRP3, Caspase-1, GSDMD, and IL-1β at both protein and gene levels (P< 0.05). Correlation analyses confirmed that these markers were positively associated with the presence of VMC. (P< 0.05). Receiver operating characteristic (ROC) analysis revealed that the combined detection of gene and protein expression achieved a higher area under the curve (AUC) than any single indicator, demonstrating superior diagnostic accuracy.
Conclusion: NLRP3 inflammasome-mediated pyroptosis plays a crucial role in the pathogenesis of viral myocarditis in children. The combined assessment of gene and protein expression levels provides a novel and more reliable approach for early diagnosis and risk evaluation of pediatric VMC, highlighting the potential of inflammasome-related biomarkers as therapeutic targets.

Keywords: children, inflammasome, NLRP3, pyroptosis, viral myocarditis