Association between Uremic Toxin Concentrations and Bone Mineral Density after Kidney Transplantation

Although uremic osteoporosis is a component of mineral and bone disorder in chronic kidney disease, uremic toxin (UT) concentrations in patients with end-stage kidney disease and bone mineral density (BMD) changes after kidney transplantation have not previously been described. We hypothesized that...

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Main Authors: Benjamin Batteux, Sandra Bodeau, Camille André, Anne-Sophie Hurtel-Lemaire, Valérie Gras-Champel, Isabelle Desailly-Henry, Kamel Masmoudi, Youssef Bennis, Ziad A. Massy, Saïd Kamel, Gabriel Choukroun, Sophie Liabeuf
Format: Article
Language:English
Published: MDPI AG 2020-11-01
Series:Toxins
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Online Access:https://www.mdpi.com/2072-6651/12/11/715
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author Benjamin Batteux
Sandra Bodeau
Camille André
Anne-Sophie Hurtel-Lemaire
Valérie Gras-Champel
Isabelle Desailly-Henry
Kamel Masmoudi
Youssef Bennis
Ziad A. Massy
Saïd Kamel
Gabriel Choukroun
Sophie Liabeuf
author_facet Benjamin Batteux
Sandra Bodeau
Camille André
Anne-Sophie Hurtel-Lemaire
Valérie Gras-Champel
Isabelle Desailly-Henry
Kamel Masmoudi
Youssef Bennis
Ziad A. Massy
Saïd Kamel
Gabriel Choukroun
Sophie Liabeuf
author_sort Benjamin Batteux
collection DOAJ
description Although uremic osteoporosis is a component of mineral and bone disorder in chronic kidney disease, uremic toxin (UT) concentrations in patients with end-stage kidney disease and bone mineral density (BMD) changes after kidney transplantation have not previously been described. We hypothesized that elevated UT concentrations at the time of transplantation could have a negative impact on bone during the early post-transplantation period. Hence, we sought to determine whether concentrations of UTs (trimethylamine-N-oxide, indoxylsulfate, p-cresylsulfate, p-cresylglucuronide, indole-3-acetic acid, hippuric acid, and 3-carboxy-4-methyl-5-propyl-furanpropionic acid) upon transplantation are predictive markers for (i) osteoporosis one month after transplantation, and (ii) a BMD decrease and the occurrence of fractures 12 and 24 months after kidney transplantation. Between 2012 and 2018, 310 kidney transplant recipients were included, and dual-energy X-ray absorptiometry was performed 1, 12, and 24 months after transplantation. The UT concentrations upon transplantation were determined by reverse-phase high-performance liquid chromatography. Indoxylsulfate concentrations upon transplantation were positively correlated with BMD one month after transplantation for the femoral neck but were not associated with osteoporosis status upon transplantation. Concentrations of the other UTs upon transplantation were not associated with osteoporosis or BMD one month after transplantation. None of the UT concentrations were associated with BMD changes and the occurrence of osteoporotic fractures 12 and 24 months after transplantation. Hence, UT concentrations at the time of kidney transplantation were not predictive markers of osteoporosis or fractures.
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spelling doaj.art-62959a0dab984bd09b01d28ba904560e2023-11-20T20:49:52ZengMDPI AGToxins2072-66512020-11-01121171510.3390/toxins12110715Association between Uremic Toxin Concentrations and Bone Mineral Density after Kidney TransplantationBenjamin Batteux0Sandra Bodeau1Camille André2Anne-Sophie Hurtel-Lemaire3Valérie Gras-Champel4Isabelle Desailly-Henry5Kamel Masmoudi6Youssef Bennis7Ziad A. Massy8Saïd Kamel9Gabriel Choukroun10Sophie Liabeuf11Department of Pharmacology, Amiens University Medical Center, F-80000 Amiens, FranceDepartment of Pharmacology, Amiens University Medical Center, F-80000 Amiens, FranceDepartment of Pharmacology, Amiens University Medical Center, F-80000 Amiens, FranceDepartment of Pharmacology, Amiens University Medical Center, F-80000 Amiens, FranceDepartment of Pharmacology, Amiens University Medical Center, F-80000 Amiens, FranceDepartment of Rheumatology, Amiens University Medical Center, F-80000 Amiens, FranceDepartment of Pharmacology, Amiens University Medical Center, F-80000 Amiens, FranceDepartment of Pharmacology, Amiens University Medical Center, F-80000 Amiens, FranceDepartment of Nephrology, Ambroise Paré University Hospital, APHP, Boulogne Billancourt, F-92100 Paris, FranceMP3CV Laboratory, EA7517, Jules Verne University of Picardie, F-80000 Amiens, FranceMP3CV Laboratory, EA7517, Jules Verne University of Picardie, F-80000 Amiens, FranceDepartment of Pharmacology, Amiens University Medical Center, F-80000 Amiens, FranceAlthough uremic osteoporosis is a component of mineral and bone disorder in chronic kidney disease, uremic toxin (UT) concentrations in patients with end-stage kidney disease and bone mineral density (BMD) changes after kidney transplantation have not previously been described. We hypothesized that elevated UT concentrations at the time of transplantation could have a negative impact on bone during the early post-transplantation period. Hence, we sought to determine whether concentrations of UTs (trimethylamine-N-oxide, indoxylsulfate, p-cresylsulfate, p-cresylglucuronide, indole-3-acetic acid, hippuric acid, and 3-carboxy-4-methyl-5-propyl-furanpropionic acid) upon transplantation are predictive markers for (i) osteoporosis one month after transplantation, and (ii) a BMD decrease and the occurrence of fractures 12 and 24 months after kidney transplantation. Between 2012 and 2018, 310 kidney transplant recipients were included, and dual-energy X-ray absorptiometry was performed 1, 12, and 24 months after transplantation. The UT concentrations upon transplantation were determined by reverse-phase high-performance liquid chromatography. Indoxylsulfate concentrations upon transplantation were positively correlated with BMD one month after transplantation for the femoral neck but were not associated with osteoporosis status upon transplantation. Concentrations of the other UTs upon transplantation were not associated with osteoporosis or BMD one month after transplantation. None of the UT concentrations were associated with BMD changes and the occurrence of osteoporotic fractures 12 and 24 months after transplantation. Hence, UT concentrations at the time of kidney transplantation were not predictive markers of osteoporosis or fractures.https://www.mdpi.com/2072-6651/12/11/715uremic toxinbone mineral densityfracturekidney transplantation
spellingShingle Benjamin Batteux
Sandra Bodeau
Camille André
Anne-Sophie Hurtel-Lemaire
Valérie Gras-Champel
Isabelle Desailly-Henry
Kamel Masmoudi
Youssef Bennis
Ziad A. Massy
Saïd Kamel
Gabriel Choukroun
Sophie Liabeuf
Association between Uremic Toxin Concentrations and Bone Mineral Density after Kidney Transplantation
Toxins
uremic toxin
bone mineral density
fracture
kidney transplantation
title Association between Uremic Toxin Concentrations and Bone Mineral Density after Kidney Transplantation
title_full Association between Uremic Toxin Concentrations and Bone Mineral Density after Kidney Transplantation
title_fullStr Association between Uremic Toxin Concentrations and Bone Mineral Density after Kidney Transplantation
title_full_unstemmed Association between Uremic Toxin Concentrations and Bone Mineral Density after Kidney Transplantation
title_short Association between Uremic Toxin Concentrations and Bone Mineral Density after Kidney Transplantation
title_sort association between uremic toxin concentrations and bone mineral density after kidney transplantation
topic uremic toxin
bone mineral density
fracture
kidney transplantation
url https://www.mdpi.com/2072-6651/12/11/715
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