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      Proposal for a New Classification of Solutes of Interest in Uremia and Hemodialysis

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          Abstract

          Uremic toxins contribute to clinical manifestations of kidney dysfunction. These toxins include organic and inorganic elements or compounds. While the kidney typically clears uremic toxins, gut dysbiosis, and tissue inflammation could lead to increased production of substances that can further the clinical manifestations of uremia. The uremic toxins are quantitatively measurable in biological fluids and have an established relationship with azotemia signs and symptoms. Their elimination is associated with mitigated uremic manifestations, while their administration to the uremic levels leads to uremic signs in animal or human models or in vitro studies. Besides, the uremic toxins have an established and plausible pathophysiologic relationship with uremic manifestations. The previous classification of uremic toxins was mainly focused on the physicochemical characteristics of these substances to divide them into three categories, (1) free water-soluble low-molecular-weight (<500 Da) solutes, (2) protein-bound, water-soluble, low molecular weight (<500 Da), (3) middle molecular weight (>500 Da and <12,000 Da), and (4) high molecular weight (>12,000 Da). Unfortunately, the classification named above was not centered around patient outcomes and quality of life among those with severe kidney failure. Therefore, a panel of experts convened virtually to provide additional insights into the current state and propose a new uremic toxin classification. This article describes the group’s consensus recommendations regarding the new classification of uremic toxins into more clinically oriented categories.

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          Author and article information

          Journal
          BPU
          Blood Purif
          10.1159/issn.0253-5068
          Blood Purification
          Blood Purif
          S. Karger AG
          0253-5068
          1421-9735
          2023
          April 2023
          09 December 2022
          : 52
          : 3
          : 233-241
          Affiliations
          [_a] aDivision of Nephrology and Hypertension, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA
          [_b] bDivision of Pulmonary and Critical Care Medicine, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA
          [_c] cRenal Division, Department of Health Sciences, ASST Santi Paolo e Carlo, Università degli Studi di Milano, Milan, Italy
          [_d] dINSERM U1018, Équipe 5, Centre de Recherche en Epidémiologie et Santé des Populations (CESP), Université Paris Saclay et Université Versailles Saint Quentin en Yvelines (UVSQ), Villejuif, France
          [_e] eService de Néphrologie et Dialyse, Assistance Publique-Hopitaux de Paris (APHP), Hôpital Universitaire Ambroise Paré, Boulogne-Billancourt, France
          [_f] fDepartment of Nephrology and Hypertension, University Medical Centre Utrecht, Utrecht, The Netherlands
          [_g] gDepartment of Renal Medicine, M99, Karolinska University Hospital, Stockholm, Sweden
          [_h] hDivision of Nephrology, University of Virginia Health System, Charlottesville, Virginia, USA
          [_i] iDepartment of Medicine, University of Padova, Padova, Italy
          [_j] jDepartment of Nephrology, Dialysis, and Transplantation, San Bortolo Hospital, International Renal Research Institute of Vicenza, Vicenza, Italy
          Author information
          https://orcid.org/0000-0003-2184-3683
          https://orcid.org/0000-0002-8494-6252
          https://orcid.org/0000-0003-4289-632X
          https://orcid.org/0000-0002-6697-4065
          Article
          528040 Blood Purif 2023;52:233–241
          10.1159/000528040
          36502799
          60324043-d8d7-4107-897c-f9a8adea6f3f
          © 2022 S. Karger AG, Basel

          Copyright: All rights reserved. No part of this publication may be translated into other languages, reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, microcopying, or by any information storage and retrieval system, without permission in writing from the publisher.

          History
          : 31 August 2022
          : 04 November 2022
          Page count
          Figures: 1, Tables: 2, Pages: 9
          Funding
          No financial support was used for the preparation of this manuscript.
          Categories
          Focus: Uremic Toxins – Review Article

          Medicine
          Artificial intelligence,Uremic toxins,Dialyzer types,End-stage kidney disease,Chronic kidney disease,Biomarkers

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