Identification of common diagnostic genes and molecular pathways in endometriosis and systemic lupus erythematosus by machine learning approach and in vitro experiment
2025

Identifying Genes Linked to Endometriosis and Lupus Using Machine Learning

Sample size: 121 publication 10 minutes Evidence: moderate

Author Information

Author(s): Yang Pusheng, Zhu Yiping, Miao Yaxin, Wang Tao, Liu Wenwen, Zhang Jiaxin, Ge Beilei, Sun Jing

Primary Institution: Shanghai Key Laboratory of Maternal Fetal Medicine, Shanghai Institute of Maternal-Fetal Medicine and Gynecologic Oncology, Shanghai First Maternity and Infant Hospital, School of Medicine, Tongji University

Hypothesis

Endometriosis and systemic lupus erythematosus share common molecular characteristics and diagnostic genes.

Conclusion

The study identified four co-diagnostic genes that may aid in the early diagnosis and targeted therapy for endometriosis and systemic lupus erythematosus.

Supporting Evidence

  • Four co-diagnostic genes (PMP22, QSOX1, REV3L, SP110) were identified for endometriosis and SLE.
  • The AUC value of the four co-diagnostic genes was higher than 0.85 in both cohorts.
  • Functional enrichment analysis showed significant pathways related to DNA replication and cell adhesion.
  • Tributyrin was found to act on all four co-diagnostic genes.

Takeaway

Researchers found four genes that can help doctors diagnose two diseases, endometriosis and lupus, more easily.

Methodology

The study used GEO datasets to identify differentially expressed genes and constructed prediction signatures using LASSO logistic regression.

Potential Biases

Potential biases due to reliance on existing datasets and limited clinical validation.

Limitations

The study relied on public databases with a small sample size for clinical validation and requires further in vivo and in vitro experiments.

Participant Demographics

The study included samples from women with endometriosis and systemic lupus erythematosus.

Statistical Information

P-Value

p<0.05

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.7150/ijms.101754

Want to read the original?

Access the complete publication on the publisher's website

View Original Publication