Allograft function and muscle mass evolution after kidney transplantation.


Journal

Journal of cachexia, sarcopenia and muscle
ISSN: 2190-6009
Titre abrégé: J Cachexia Sarcopenia Muscle
Pays: Germany
ID NLM: 101552883

Informations de publication

Date de publication:
12 2022
Historique:
revised: 07 07 2022
received: 14 01 2022
accepted: 15 07 2022
pubmed: 16 9 2022
medline: 15 12 2022
entrez: 15 9 2022
Statut: ppublish

Résumé

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. 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. 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 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.

Sections du résumé

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
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.

Identifiants

pubmed: 36106518
doi: 10.1002/jcsm.13066
pmc: PMC9745471
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2875-2887

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

© 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.

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Auteurs

François Gaillard (F)

Service de Transplantation, Néphrologie et Immunologie Clinique, Hôpital Edouard Herriot et faculté de médecine, Université Lyon 1, Lyon, France.

Mélissa Ould Rabah (M)

Service de Physiologie, Hôpital Necker-Enfants Malades, Assistance-Publique-Hôpitaux de Paris, Paris, France.
Faculté de médecine, Université de Paris-Cité, Paris, France.

Nicolas Garcelon (N)

Université de Paris-Cité, Imagine Institute, Data Science Platform, INSERM UMR 1163, Paris, France.

Malik Touam (M)

Service de Néphrologie et Transplantation, Hôpital Necker-Enfants Malades, Assistance-Publique-Hôpitaux de Paris, Paris, France.

Antoine Neuraz (A)

Service d'Informatique Médical, Hôpital Necker-Enfants Malades, Assistance-Publique-Hôpitaux de Paris, Paris, France.

Christophe Legendre (C)

Faculté de médecine, Université de Paris-Cité, Paris, France.
Service de Néphrologie et Transplantation, Hôpital Necker-Enfants Malades, Assistance-Publique-Hôpitaux de Paris, Paris, France.
Institut Necker-Enfants Malades, INSERM U1151, Paris, France.

Dany Anglicheau (D)

Faculté de médecine, Université de Paris-Cité, Paris, France.
Service de Néphrologie et Transplantation, Hôpital Necker-Enfants Malades, Assistance-Publique-Hôpitaux de Paris, Paris, France.
Institut Necker-Enfants Malades, INSERM U1151, Paris, France.

Dominique Prié (D)

Service de Physiologie, Hôpital Necker-Enfants Malades, Assistance-Publique-Hôpitaux de Paris, Paris, France.
Faculté de médecine, Université de Paris-Cité, Paris, France.
Institut Necker-Enfants Malades, INSERM U1151, Paris, France.

Frank Bienaimé (F)

Service de Physiologie, Hôpital Necker-Enfants Malades, Assistance-Publique-Hôpitaux de Paris, Paris, France.
Faculté de médecine, Université de Paris-Cité, Paris, France.
Institut Necker-Enfants Malades, INSERM U1151, Paris, France.

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