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Allograft function and muscle mass evolution after kidney transplantation

BACKGROUND: Advanced chronic kidney disease is associated with muscle wasting, but how glomerular filtration rate (GFR) recovery after kidney transplantation is associated with muscle mass is unknown. METHODS: We took advantage of the simultaneous measurement of GFR (using iohexol plasma clearance;...

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Autores principales: Gaillard, François, Ould Rabah, Mélissa, Garcelon, Nicolas, Touam, Malik, Neuraz, Antoine, Legendre, Christophe, Anglicheau, Dany, Prié, Dominique, Bienaimé, Frank
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9745471/
https://www.ncbi.nlm.nih.gov/pubmed/36106518
http://dx.doi.org/10.1002/jcsm.13066
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author Gaillard, François
Ould Rabah, Mélissa
Garcelon, Nicolas
Touam, Malik
Neuraz, Antoine
Legendre, Christophe
Anglicheau, Dany
Prié, Dominique
Bienaimé, Frank
author_facet Gaillard, François
Ould Rabah, Mélissa
Garcelon, Nicolas
Touam, Malik
Neuraz, Antoine
Legendre, Christophe
Anglicheau, Dany
Prié, Dominique
Bienaimé, Frank
author_sort Gaillard, François
collection PubMed
description BACKGROUND: Advanced chronic kidney disease is associated with muscle wasting, but how glomerular filtration rate (GFR) recovery after kidney transplantation is associated with muscle mass is unknown. METHODS: We took advantage of the simultaneous measurement of GFR (using iohexol plasma clearance; ioGFR) and creatinine excretion rate (a surrogate marker of muscle mass; CER) performed 3 months after transplantation and at a later time point at our institution to investigate the interplay between allograft function, muscle mass, and outcome in kidney transplant recipients. RESULTS: Between June 2005 and October 2019, 1319 successive kidney transplant recipients (mean age 50.4 ± 14.6; 38.7% female) underwent GFR measurement at our institution 3 months after kidney transplantation. CER (CER(3)) and ioGFR (ioGFR(3)) were 7.7 ± 2.6 μmol/min and 53 ± 17.1 mL/min/1.73 m(2), respectively. Multivariable analysis identified female gender, older donor and recipient age, reduced body mass index, coronary disease, dialysis history, proteinuria, and reduced ioGFR(3) as independent predictors of low CER(3) (ioGFR(3): β coefficient 0.19 [95% confidence interval 0.14 to 0.24]). A total of 1165 patients had a subsequent CER measurement after a median follow‐up of 9.5 months. Of them, 373 (32%) experienced an increase in CER > 10%, while 222 (19%) showed a CER decrease of more than 10%. Multivariable analysis adjusted for CER(3) and other confounders identified ioGFR(3) as an independent predictor of CER at follow‐up (β coefficient 0.11 [95% confidence interval 0.07 to 0.16]). In multivariable Cox analysis, reduced CER at 3 months or at follow‐up were consistently associated with mortality (hazard ratio [95% confidence interval] at 3 months: 0.82 [0.74 to 0.91]; at follow‐up: 0.79 [0.69 to 0.99]) but not with graft loss. CONCLUSIONS: Glomerular filtration rate recovery is a determinant of muscle mass variation after kidney transplantation. Early interventions targeting muscle mass gain may be beneficial for kidney transplant recipients.
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spelling pubmed-97454712022-12-14 Allograft function and muscle mass evolution after kidney transplantation Gaillard, François Ould Rabah, Mélissa Garcelon, Nicolas Touam, Malik Neuraz, Antoine Legendre, Christophe Anglicheau, Dany Prié, Dominique Bienaimé, Frank J Cachexia Sarcopenia Muscle Original Articles BACKGROUND: Advanced chronic kidney disease is associated with muscle wasting, but how glomerular filtration rate (GFR) recovery after kidney transplantation is associated with muscle mass is unknown. METHODS: We took advantage of the simultaneous measurement of GFR (using iohexol plasma clearance; ioGFR) and creatinine excretion rate (a surrogate marker of muscle mass; CER) performed 3 months after transplantation and at a later time point at our institution to investigate the interplay between allograft function, muscle mass, and outcome in kidney transplant recipients. RESULTS: Between June 2005 and October 2019, 1319 successive kidney transplant recipients (mean age 50.4 ± 14.6; 38.7% female) underwent GFR measurement at our institution 3 months after kidney transplantation. CER (CER(3)) and ioGFR (ioGFR(3)) were 7.7 ± 2.6 μmol/min and 53 ± 17.1 mL/min/1.73 m(2), respectively. Multivariable analysis identified female gender, older donor and recipient age, reduced body mass index, coronary disease, dialysis history, proteinuria, and reduced ioGFR(3) as independent predictors of low CER(3) (ioGFR(3): β coefficient 0.19 [95% confidence interval 0.14 to 0.24]). A total of 1165 patients had a subsequent CER measurement after a median follow‐up of 9.5 months. Of them, 373 (32%) experienced an increase in CER > 10%, while 222 (19%) showed a CER decrease of more than 10%. Multivariable analysis adjusted for CER(3) and other confounders identified ioGFR(3) as an independent predictor of CER at follow‐up (β coefficient 0.11 [95% confidence interval 0.07 to 0.16]). In multivariable Cox analysis, reduced CER at 3 months or at follow‐up were consistently associated with mortality (hazard ratio [95% confidence interval] at 3 months: 0.82 [0.74 to 0.91]; at follow‐up: 0.79 [0.69 to 0.99]) but not with graft loss. CONCLUSIONS: Glomerular filtration rate recovery is a determinant of muscle mass variation after kidney transplantation. Early interventions targeting muscle mass gain may be beneficial for kidney transplant recipients. John Wiley and Sons Inc. 2022-09-15 2022-12 /pmc/articles/PMC9745471/ /pubmed/36106518 http://dx.doi.org/10.1002/jcsm.13066 Text en © 2022 The Authors. Journal of Cachexia, Sarcopenia and Muscle published by John Wiley & Sons Ltd on behalf of Society on Sarcopenia, Cachexia and Wasting Disorders. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Gaillard, François
Ould Rabah, Mélissa
Garcelon, Nicolas
Touam, Malik
Neuraz, Antoine
Legendre, Christophe
Anglicheau, Dany
Prié, Dominique
Bienaimé, Frank
Allograft function and muscle mass evolution after kidney transplantation
title Allograft function and muscle mass evolution after kidney transplantation
title_full Allograft function and muscle mass evolution after kidney transplantation
title_fullStr Allograft function and muscle mass evolution after kidney transplantation
title_full_unstemmed Allograft function and muscle mass evolution after kidney transplantation
title_short Allograft function and muscle mass evolution after kidney transplantation
title_sort allograft function and muscle mass evolution after kidney transplantation
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9745471/
https://www.ncbi.nlm.nih.gov/pubmed/36106518
http://dx.doi.org/10.1002/jcsm.13066
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