IntroductionThe low incidence of intradialytic hypotension (IDH) in high-volume (HV) hemodiafiltration (HDF) may help maintaining gut perfusion during treatment. Preservation of gut endothelial integrity would limit or prevent bacterial translocation and subsequent systemic inflammation, which may contribute to the low mortality rate in HV-HDF. MethodsForty patients were cross-over randomized to S-HD, cool HD (C-HD) and HDF (low-volume [LV] and HV, convection volumes 15 L resp. ≥23 L/session), each for 2 weeks. Quantitative assessment of microbial DNA (mDNA) in blood was performed before and after dialysis by 16S-23S interspace profiling after DNA isolation. The intradialytic acute phase response (APR) was evaluated by high-sensitivity CRP (hs-CRP), IL-6 receptor (IL-6R), soluble CD14 (sCD14) and vascular-cell-adhesion molecule-1 (VCAM-1). Differences between modalities were primary objectives. ResultsMDNA was absent in all samples. IL-6R, sCD14, and VCAM-1 increased equally in all modalities (median increase resp.: 12.5%, 14.0%, 14.8%, P<0.05). Hs-CRP increased only in C-HD and HV-HDF (median increase: 12.6%, P<0.05). After correction for hemoconcentration, most APR-markers decreased (median: sCD14 -11.3% and VCAM-1 -14.4% in all modalities; IL-6R -13.4% in C-HD, LV- and HV-HDF; P<0.05). Hs-CRP only decreased in C-HD (-13.5%, P=0.004). Conclusions1) Circulating mDNA could not be demonstrated; 2) while in the crude analysis a similar APR was noted in all modalities, individual markers remained stable or declined after correction for hemoconcentration; 3) as neither bacterial translocation nor an APR was observed in either modality, it is highly unlikely that the superior survival of HV-HDF is explained by superior preservation of gut integrity.