# Effects of Hemodiafiltration Versus Hemodialysis on Uremic Toxins, Inflammatory Markers, Anemia, and Nutritional Parameters: A Systematic Review and Meta-Analysis

**Authors:** Wannasit Wathanavasin, Solos Jaturapisanukul, Preeyaporn Janwetchasil, Charat Thongprayoon, Wisit Cheungpasitporn, Tibor Fülöp

PMC · DOI: 10.3390/toxins18020086 · Toxins · 2026-02-06

## TL;DR

This study compares hemodiafiltration and hemodialysis, finding that hemodiafiltration better reduces certain toxins and inflammation markers in dialysis patients.

## Contribution

A systematic review and meta-analysis showing hemodiafiltration's superior clearance of uremic toxins and inflammatory markers compared to hemodialysis.

## Key findings

- HDF significantly reduces serum phosphorus and β2-microglobulin compared to HD.
- HDF lowers serum urea, CRP, and weekly erythropoietin requirements.
- Higher convective volumes in HDF correlate with greater reductions in β2-microglobulin and CRP.

## Abstract

Hemodiafiltration (HDF) is increasingly used because of its enhanced theoretical clearance of diverse uremic toxins, particularly middle molecules and inflammatory cytokines, relative to conventional hemodialysis (HD), yet evidence on its biochemical benefits remains conflicting. Therefore, this meta-analysis was performed to evaluate the effects of HDF versus HD on uremic toxins, inflammation, anemia, and nutritional parameters. A systematic literature search was conducted using PubMed, Scopus, and the Cochrane Central Register of Controlled Trials to identify relevant studies. Only randomized controlled trials (RCTs) were included. Random-effects meta-analyses were performed to evaluate changes in the prespecified outcomes. Twenty-four RCTs involving 6072 dialysis patients were included. Compared with conventional HD, HDF was associated with significant reductions in serum phosphorus (weighted mean difference [WMD] −0.28 mg/dL; 95% CI −0.44 to −0.12) and β2-microglobulin (WMD −4.84 mg/dL; 95% CI −6.13 to −3.54). HDF also significantly reduced serum urea and C-reactive protein (CRP) levels, along with weekly erythropoietin requirements. Serum albumin levels were slightly but significantly lower in the HDF group than in the conventional HD group (WMD –0.06 g/dL; 95% CI −0.10 to −0.01); however, the clinical significance of such a difference remains uncertain. Higher convective volumes were identified as a key determinant of greater reductions in β2-microglobulin and CRP. Compared with conventional HD, HDF demonstrated superior reductions in several surrogate endpoints, including serum phosphorus, urea, β2-microglobulin, CRP, and weekly erythropoietin requirements. Reduced need for phosphate binders and anemia management may lower treatment-related costs.

## Linked entities

- **Chemicals:** phosphorus (PubChem CID 139579), urea (PubChem CID 1176)

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, 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}, TF (transferrin) [NCBI Gene 7018] {aka HEL-S-71p, PRO1557, PRO2086, TFQTL1}, EPO (erythropoietin) [NCBI Gene 2056] {aka DBAL, ECYT5, EP, MVCD2}, HLA-G (major histocompatibility complex, class I, G) [NCBI Gene 3135] {aka MHC-G}, PCS [NCBI Gene 8075], PTH (parathyroid hormone) [NCBI Gene 5741] {aka FIH1, PTH1}
- **Diseases:** Uremic (MESH:D006463), cardiovascular disease (MESH:D002318), CKD-MBD (MESH:D012080), ESKD (MESH:D007676), vascular dysfunction (MESH:D002561), Anemia (MESH:D000740), amyloidosis (MESH:D000686), IS (MESH:C563094), diabetes (MESH:D003920), DM (MESH:D009223), injury to (MESH:D014947), Inflammatory (MESH:D007249), hypoalbuminemia (MESH:D034141), PEW (MESH:D011502)
- **Chemicals:** Urea (MESH:D014508), TSAT (-), IS (MESH:D007200), p-Cresyl Sulfate (MESH:C408690), vitamin D (MESH:D014807), Phosphorus (MESH:D010758), phosphate (MESH:D010710), Pi (MESH:D010716), water (MESH:D014867), iron (MESH:D007501)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

67 references — full list in the complete paper: https://tomesphere.com/paper/PMC12944842/full.md

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Source: https://tomesphere.com/paper/PMC12944842