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March 12, 2026Brazilian Journal of Medical and Biological Research0 citationsOpen Access

Disulfidptosis modification patterns are involved in the immune microenvironment regulation of septic acute respiratory distress syndrome

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QZQibo ZhangJGJunke Ge

Key Points

  • To explore how disulfidptosis influences the immune microenvironment in septic acute respiratory distress syndrome (ARDS).
  • Collected 16 disulfidptosis-related genes from a prior study.
  • Analyzed gene expression data from sepsis and septic ARDS samples in the Gene Expression Omnibus database.
  • Constructed a risk score model using 6 disulfidptosis-related genes to differentiate septic patients from those with septic ARDS.
  • Divided septic ARDS patients into subtypes based on disulfidptosis modification patterns and investigated their immune characteristics.
  • Developed diagnostic models using 3 hub genes for classification of the ARDS subtypes.
  • The immune microenvironment in septic ARDS patients was notably different from that in sepsis patients.
  • A reliable risk score model was established, effectively distinguishing septic patients from those with septic ARDS.
  • Two distinct subtypes of septic ARDS were identified based on disulfidptosis modification patterns.
  • Three diagnostic models were created to accurately classify the two septic ARDS subtypes.

Abstract

Disulfidptosis is a new form of programmed cell death. However, there is limited information available regarding the impact of disulfidptosis on septic acute respiratory distress syndrome (ARDS). The 16 disulfidptosis-related genes (DRGs) were collected from a previous study. Gene expression data of sepsis and septic ARDS samples were downloaded from the Gene Expression Omnibus database. The risk score model in septic ARDS was constructed based on the DRGs, followed by the investigation of immune microenvironment in septic ARDS patients. Furthermore, septic ARDS patients were divided into different subtypes based on disulfidptosis modification patterns, and their immune characteristics were investigated. Finally, the differentially expressed genes among different subtypes were identified, and a diagnostic model was constructed. The risk score model based on 6 DRGs was constructed to distinguish sepsis patients from septic ARDS patients, with good performance. The immune microenvironment in septic ARDS patients was slightly different from sepsis patients. Additionally, septic ARDS patients were divided into two subtypes based on DRGs. Finally, three diagnostic models based on 3 hub genes were constructed to classify the two subtypes in septic ARDS patients. Our findings indicated that disulfidptosis might play a role in the immune microenvironment of septic ARDS.

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Cite This Study

Zhang et al. (2026) studied this question.

synapsesocial.com/papers/69b2587296eeacc4fcec82b4https://doi.org/10.1590/1414-431x2025e14932
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