# Resolving Inflammation in CKD: The Potential of SPMs and Omega-3 Derivatives as Biomarkers and Therapeutics

**Authors:** Beata Franczyk, Wiktoria Lisińska, Katarzyna Hossa, Kinga Katańska, Anna Wieczorek, Aleksandra Prusak, Zuzanna Biegała, Jacek Rysz, Ewelina Młynarska

PMC · DOI: 10.3390/biomedicines14030619 · Biomedicines · 2026-03-10

## TL;DR

This review explores how specialized pro-resolving mediators (SPMs) and omega-3 derivatives may help reduce inflammation and slow kidney disease progression.

## Contribution

The paper synthesizes current knowledge on SPMs and omega-3 derivatives as potential biomarkers and therapies for CKD-related inflammation.

## Key findings

- SPMs show nephroprotective and antifibrotic effects in kidney disease models.
- EPA/DHA supplementation reduces inflammatory biomarkers in CKD patients.
- Advanced analytical methods like LC-MS/MS can monitor inflammation phases in CKD.

## Abstract

Chronic kidney disease (CKD) affects more than 10% of the population and is associated with a persistent, low-grade inflammatory state that accelerates tubulointerstitial fibrosis, worsens prognosis, and increases cardiovascular risk. This review aims to synthesize current knowledge on specialized pro-resolving mediators (SPMs) in the context of CKD pathophysiology, biomarkers, and therapeutic potential. We discuss key anti-inflammatory and pro-resolving mechanisms of SPMs that translate into nephroprotective and antifibrotic effects in experimental kidney models. The review summarizes data on EPA/DHA supplementation, including its impact on lipid profiles, inflammatory biomarkers (CRP, IL-6, TNF-α), and oxidative stress in patients with CKD. We also highlight contemporary analytical methods for biomarker assessment (LC-MS/MS, UHPLC-HRMS) and their potential for monitoring inflammatory activity across its phases (initiation, attenuation, resolution), CKD progression, and responses to ω-3/SPM-based interventions. Finally, we discuss the therapeutic potential of SPMs, as well as safety considerations and pharmacological interactions. In conclusion, SPMs and ω-3-derived mediators represent promising research and clinical targets as markers and modulators of inflammation in CKD, but require further validation in well-designed prospective studies.

## Linked entities

- **Chemicals:** EPA (PubChem CID 446284), DHA (PubChem CID 15608515)

## Full-text entities

- **Genes:** IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}
- **Diseases:** tubulointerstitial fibrosis (MESH:D005355), Inflammation (MESH:D007249), CKD (MESH:D051436)
- **Chemicals:** Omega-3 (-), lipid (MESH:D008055), DHA (MESH:C027493)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC13024605/full.md

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13024605/full.md

## References

182 references — full list in the complete paper: https://tomesphere.com/paper/PMC13024605/full.md

---
Source: https://tomesphere.com/paper/PMC13024605