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February 7, 2025Frontiers in ImmunologyOpen Access

Cuproptosis-related NUDT16 and immune-related CXCL12 demonstrate exceptional diagnostic performance for IPF with 0.92 AUROC.

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Why the study?

Idiopathic pulmonary fibrosis has high mortality and limited treatments, prompting exploration of cuproptosis- and immune-related hub genes as potential diagnostic biomarkers and therapeutic targets.

Population

Four microarray datasets from the Gene Expression Omnibus (GEO) collection for IPF

Design

Bioinformatics and single-cell RNA-seq analysis

Key result

Cuproptosis-related gene NUDT16 and immune-related gene CXCL12 demonstrated exceptional diagnostic performance for idiopathic pulmonary fibrosis, each achieving an AUROC of 0.92.

Authors

CJChengji JinJLJia LiQLQiaoyu Li

Discussion

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Overview

Hypothesis-generating for IPF biomarkers; requires prospective validation before any diagnostic use.

Study Design

Type

Observational (n=303)

Structured PICO

P
Population
303 samples from patients with idiopathic pulmonary fibrosis and healthy controls analyzed via bioinformatics and single-cell sequencing to identify diagnostic biomarkers.
O
Outcome
Diagnostic value of cuproptosis-related and immune-related hub genes for IPFsurrogate

Main Result

Effect estimate: AUROC 0.92 (95% CI 0.86-0.98)

Bioinformatics analysis identified five cuproptosis-related and four immune-related hub genes as potential diagnostic biomarkers and therapeutic targets for idiopathic pulmonary fibrosis.

Limitations

  • Limitations were not explicitly stated in the provided text.

Cite This Study

Jin et al. (2025) conducted an observational in Idiopathic pulmonary fibrosis (IPF) (n=303). Cuproptosis and immune-related gene expression vs. Healthy controls was evaluated on Diagnostic accuracy (AUROC) for idiopathic pulmonary fibrosis (AUROC 0.92, 95% CI 0.86-0.98). Cuproptosis-related gene NUDT16 and immune-related gene CXCL12 demonstrated exceptional diagnostic performance for idiopathic pulmonary fibrosis, each achieving an AUROC of 0.92.

synapsesocial.com/papers/6aa3a3fedd5797a3831aa394https://doi.org/10.3389/fimmu.2025.1458341
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