Advances in multi-omics and therapeutic studies of Henoch-Schönlein purpura
Henoch-Schönlein purpura (HSP) is a vasculopathic disease due to lesions in blood vessels, and patients with HSP presenting with renal injury are at risk of further progression to end-stage renal disease, resulting in a severe disease burden, the pathogenesis of which is currently unclear. By integrating multi-omics data, biomarkers and signaling pathways that are specifically expressed in HSP can be screened, thus finding new perspectives for resolving the pathogenesis of HSP. The aim of this review is to explore the developmental pathways of HSP and to reveal key biomarkers and therapeutic targets. Finally, we discuss the therapeutic approaches to HSP, with the hope that these insights will drive the future development of personalized medicine and improve patient prognosis and quality of life.
Authors
- Rongguang Zhang (ORCID: https://orcid.org/0000-0001-9961-2434)
- Shenggang Sang (ORCID: https://orcid.org/0000-0002-7026-1754)
- Fei Gao (ORCID: https://orcid.org/0000-0002-1235-8005)
- Wenjuan Liang (ORCID: https://orcid.org/0000-0002-6185-4259)
- Lu Wang (ORCID: https://orcid.org/0000-0002-0458-8011)
- Min Xu (ORCID: https://orcid.org/0000-0002-2325-3532)
- Z. Y. Wei (ORCID: https://orcid.org/0000-0002-3834-3397)
Institutions
- Hainan Medical University (CN)
Publication Details
- Journal
- The Italian Journal of Pediatrics/Italian journal of pediatrics
- Published
- 2025-12-05
- DOI
- https://doi.org/10.1186/s13052-025-02174-6
- Primary Topic
- Vasculitis and related conditions
- Type
- article
- Field-Weighted Citation Impact
- 0.00