Literature DB >> 30201548

Transplantation of a Gitelman Syndrome Kidney Ameliorates Hypertension: A Case Report.

Daniel Stewart1, Daniela Iancu2, Emma Ashton3, Aisling E Courtney4, Andrew Connor5, Stephen B Walsh6.   

Abstract

Gitelman syndrome is caused by inactivating mutations of the gene that encodes the renal sodium/chloride cotransporter (NCC; encoded by SLC12A3), resulting in hypokalemia, hypomagnesemia, hypocalciuria, and metabolic alkalosis. Renal salt wasting commonly provokes mild hypotension. The paucity of previous kidney transplants from donors with known tubulopathies suggests that such conditions may be considered contraindications to donation. A 76-year-old man received a live unrelated kidney transplant from a donor with known Gitelman syndrome secondary to a pathogenic mutation of SLC12A3. Immediate graft function preceded the emergence of the Gitelman syndrome biochemical phenotype and blood pressure subsequently improved. The recipient developed unexpected hyponatremia. Potential causes are discussed, including the possibility that it paralleled the physiologic changes seen in the high-volume state of thiazide-induced hyponatremia. Transplanted kidneys are subject to nephrotoxicity from the use of calcineurin inhibitors. Acquired Gitelman syndrome may confer a potential long-term advantage to the recipient through both improved blood pressure control and protection against the calcineurin inhibitor-induced side-effect profile caused by NCC overactivation. Both the donor and recipient remain well. In conclusion, Gitelman syndrome need not preclude kidney donation and transference of the phenotype may have benefits for the recipient.
Copyright © 2018 National Kidney Foundation, Inc. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  BP control; Gitelman syndrome; blood pressure (BP); case report; hypertension; kidney transplantation; phenotype transference

Year:  2018        PMID: 30201548     DOI: 10.1053/j.ajkd.2018.06.030

Source DB:  PubMed          Journal:  Am J Kidney Dis        ISSN: 0272-6386            Impact factor:   8.860


  3 in total

1.  A novel compound heterozygous mutation of SLC12A3 gene in a Chinese pedigree with Gitelman syndrome.

Authors:  Xin Wang; Yu Ding; Qi Liu; Guocan Yang
Journal:  Endocrine       Date:  2019-12-05       Impact factor: 3.633

2.  Long-term Clinical Course after Living Kidney Donation by a Patient with Gitelman Syndrome Harboring a Compound Heterozygous Mutation of the SLC12A3 Gene.

Authors:  Sahoko Kamejima; Izumi Yamamoto; Akiko Tajiri; Yudo Tanno; Ichiro Ohkido; Takashi Yokoo
Journal:  Intern Med       Date:  2020-12-15       Impact factor: 1.271

Review 3.  Molecular Basis, Diagnostic Challenges and Therapeutic Approaches of Bartter and Gitelman Syndromes: A Primer for Clinicians.

Authors:  Laura Nuñez-Gonzalez; Noa Carrera; Miguel A Garcia-Gonzalez
Journal:  Int J Mol Sci       Date:  2021-10-22       Impact factor: 5.923

  3 in total

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