<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lu R</submitter><funding>the Crosswise projects of Renji Hospital, School of Medicine, Shanghai Jiao Tong University</funding><funding>the Clinical Research Plan of SHDC</funding><pagination>2338929</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11028005</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>46(1)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>To delineate the efficacy and safety profile of hemodiafiltration with endogenous reinfusion (HFR) for uremic toxin removal in patients undergoing maintenance hemodialysis (MHD).&lt;h4>Methods&lt;/h4>Patients who have been on MHD for a period of at least 3 months were enrolled. Each subject underwent one HFR and one hemodiafiltration (HDF) treatment. Blood samples were collected before and after a single HFR or HDF treatment to test uremic toxin levels and to calculate clearance rate. The primary efficacy endpoint was to compare uremic toxin levels of indoxyl sulfate (IS), λ-free light chains (λFLC), and β&lt;sub>2&lt;/sub>-microglobulin (β&lt;sub>2&lt;/sub>-MG) before and after HFR treatment. Secondary efficacy endpoints was to compare the levels of urea, interleukin-6 (IL-6), P-cresol, chitinase-3-like protein 1 (YKL-40), leptin (LEP), hippuric acid (HPA), trimethylamine N-oxide (TMAO), asymmetric dimethylarginine (ADMA), tumor necrosis factor-α (TNF-α), fibroblast growth factor 23 (FGF23) before and after HFR treatment. The study also undertook a comparative analysis of uremic toxin clearance between a single HFR and HDF treatment. Meanwhile, the lever of serum albumin and branched-chain amino acids before and after a single HFR or HDF treatment were compared. In terms of safety, the study was meticulous in recording vital signs and the incidence of adverse events throughout its duration.&lt;h4>Results&lt;/h4>The study enrolled 20 patients. After a single HFR treatment, levels of IS, λFLC, β&lt;sub>2&lt;/sub>-MG, IL-6, P-cresol, YKL-40, LEP, HPA, TMAO, ADMA, TNF-α, and FGF23 significantly decreased (&lt;i>p&lt;/i> &lt; 0.001 for all). The clearance rates of λFLC, β&lt;sub>2&lt;/sub>-MG, IL-6, LEP, and TNF-α were significantly higher in HFR compared to HDF (&lt;i>p&lt;/i> values: 0.036, 0.042, 0.041, 0.019, and 0.036, respectively). Compared with pre-HFR and post-HFR treatment, levels of serum albumin, valine, and isoleucine showed no significant difference (&lt;i>p&lt;/i> > 0.05), while post-HDF, levels of serum albumin significantly decreased (&lt;i>p&lt;/i> = 0.000).&lt;h4>Conclusion&lt;/h4>HFR treatment effectively eliminates uremic toxins from the bloodstream of patients undergoing MHD, especially protein-bound toxins and large middle-molecule toxins. Additionally, it retains essential physiological compounds like albumin and branched-chain amino acids, underscoring its commendable safety profile.</pubmed_abstract><journal>Renal failure</journal><pubmed_title>Hemodiafiltration with endogenous reinfusion for uremic toxin removal in patients undergoing maintenance hemodialysis: a pilot study.</pubmed_title><pmcid>PMC11028005</pmcid><funding_grant_id>IIT-2023-0070</funding_grant_id><funding_grant_id>SHDC2020CR4004</funding_grant_id><pubmed_authors>Fang Y</pubmed_authors><pubmed_authors>Qian Y</pubmed_authors><pubmed_authors>Xie Y</pubmed_authors><pubmed_authors>Gu L</pubmed_authors><pubmed_authors>Zeng X</pubmed_authors><pubmed_authors>Wu W</pubmed_authors><pubmed_authors>Liu T</pubmed_authors><pubmed_authors>Zhou Y</pubmed_authors><pubmed_authors>Lu R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Hemodiafiltration with endogenous reinfusion for uremic toxin removal in patients undergoing maintenance hemodialysis: a pilot study.</name><description>&lt;h4>Objective&lt;/h4>To delineate the efficacy and safety profile of hemodiafiltration with endogenous reinfusion (HFR) for uremic toxin removal in patients undergoing maintenance hemodialysis (MHD).&lt;h4>Methods&lt;/h4>Patients who have been on MHD for a period of at least 3 months were enrolled. Each subject underwent one HFR and one hemodiafiltration (HDF) treatment. Blood samples were collected before and after a single HFR or HDF treatment to test uremic toxin levels and to calculate clearance rate. The primary efficacy endpoint was to compare uremic toxin levels of indoxyl sulfate (IS), λ-free light chains (λFLC), and β&lt;sub>2&lt;/sub>-microglobulin (β&lt;sub>2&lt;/sub>-MG) before and after HFR treatment. Secondary efficacy endpoints was to compare the levels of urea, interleukin-6 (IL-6), P-cresol, chitinase-3-like protein 1 (YKL-40), leptin (LEP), hippuric acid (HPA), trimethylamine N-oxide (TMAO), asymmetric dimethylarginine (ADMA), tumor necrosis factor-α (TNF-α), fibroblast growth factor 23 (FGF23) before and after HFR treatment. The study also undertook a comparative analysis of uremic toxin clearance between a single HFR and HDF treatment. Meanwhile, the lever of serum albumin and branched-chain amino acids before and after a single HFR or HDF treatment were compared. In terms of safety, the study was meticulous in recording vital signs and the incidence of adverse events throughout its duration.&lt;h4>Results&lt;/h4>The study enrolled 20 patients. After a single HFR treatment, levels of IS, λFLC, β&lt;sub>2&lt;/sub>-MG, IL-6, P-cresol, YKL-40, LEP, HPA, TMAO, ADMA, TNF-α, and FGF23 significantly decreased (&lt;i>p&lt;/i> &lt; 0.001 for all). The clearance rates of λFLC, β&lt;sub>2&lt;/sub>-MG, IL-6, LEP, and TNF-α were significantly higher in HFR compared to HDF (&lt;i>p&lt;/i> values: 0.036, 0.042, 0.041, 0.019, and 0.036, respectively). Compared with pre-HFR and post-HFR treatment, levels of serum albumin, valine, and isoleucine showed no significant difference (&lt;i>p&lt;/i> > 0.05), while post-HDF, levels of serum albumin significantly decreased (&lt;i>p&lt;/i> = 0.000).&lt;h4>Conclusion&lt;/h4>HFR treatment effectively eliminates uremic toxins from the bloodstream of patients undergoing MHD, especially protein-bound toxins and large middle-molecule toxins. Additionally, it retains essential physiological compounds like albumin and branched-chain amino acids, underscoring its commendable safety profile.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Dec</publication><modification>2026-06-01T21:19:48.213Z</modification><creation>2026-05-21T03:08:10.356Z</creation></dates><accession>S-EPMC11028005</accession><cross_references><pubmed>38632963</pubmed><doi>10.1080/0886022X.2024.2338929</doi></cross_references></HashMap>