Improving a Rare Metabolic Disorder Through Kidney Transplantation: A Case Report of a Patient With Lysinuric Protein Intolerance.
Amino acids
Case report
Citrulline
Index Words: Lysinuric protein intolerance (LPI)
Kidney transplantation
Metabolic disorder
Renal failure
SLC7A7
Whole-exome sequencing (WES)
Journal
American journal of kidney diseases : the official journal of the National Kidney Foundation
ISSN: 1523-6838
Titre abrégé: Am J Kidney Dis
Pays: United States
ID NLM: 8110075
Informations de publication
Date de publication:
04 2023
04 2023
Historique:
received:
24
02
2022
accepted:
05
08
2022
pubmed:
13
10
2022
medline:
28
3
2023
entrez:
12
10
2022
Statut:
ppublish
Résumé
Lysinuric protein intolerance (LPI) is a rare metabolic disorder with reduced renal and intestinal reabsorption of ornithine, lysine, and arginine. It is due to variants in SLC7A7, the gene encoding y+L amino acid transporter 1 (y+LAT1), which lead to urea cycle defects with protein intolerance. Chronic kidney disease in lysinuric protein intolerance is common and can progress to kidney failure and initiation of kidney replacement therapy. Kidney transplantation could in theory improve urine levels and, consequently, plasma levels of these amino acids and therefore improve clinical symptoms, as well as protein intolerance, in patients with lysinuric protein intolerance. However, data on kidney transplantation in patients with lysinuric protein intolerance are limited, and up until now no data on clinical and biochemical improvement after kidney transplantation have been reported. In this case report we describe a rare case of kidney transplantation in a lysinuric protein intolerance patient with substantial improvement in protein tolerance; in plasma and urine levels of ornithine, lysine, and arginine; and in lysinuric protein intolerance symptoms.
Identifiants
pubmed: 36223829
pii: S0272-6386(22)00931-3
doi: 10.1053/j.ajkd.2022.08.019
pii:
doi:
Substances chimiques
Lysine
K3Z4F929H6
Arginine
94ZLA3W45F
Ornithine
E524N2IXA3
SLC7A7 protein, human
0
Amino Acid Transport System y+L
0
Types de publication
Case Reports
Langues
eng
Sous-ensembles de citation
IM
Pagination
493-496Informations de copyright
Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved.