Raised CK and acute kidney injury following intense exercise in three patients with a history of exercise intolerance due to homozygous mutations in SLC2A9.


Journal

Neuromuscular disorders : NMD
ISSN: 1873-2364
Titre abrégé: Neuromuscul Disord
Pays: England
ID NLM: 9111470

Informations de publication

Date de publication:
Jan 2024
Historique:
received: 31 07 2023
revised: 01 11 2023
accepted: 27 11 2023
medline: 24 1 2024
pubmed: 28 12 2023
entrez: 27 12 2023
Statut: ppublish

Résumé

Acute rhabdomyolysis (AR) leading to acute kidney injury has many underlying etiologies, however, when the primary trigger is exercise, the most usual underlying cause is either a genetic muscle disorder or unaccustomed intense exercise in a healthy individual. Three adult men presented with a history of exercise intolerance and episodes of acute renal impairment following intense exercise, thought to be due to AR in the case of two, and dehydration in one. The baseline serum CK was mildly raised between attacks in all three patients and acutely raised during attacks in two of the three patients. Following referral to a specialized neuromuscular centre, further investigation identified very low serum urate (<12 umol/L). In all three men, genetic studies confirmed homozygous mutations in SLC2A9, which encodes for facilitated glucose transporter member 9 (GLUT9), a major regulator of urate homeostasis. Hereditary hypouricaemia should be considered in people presenting with acute kidney injury related to intense exercise. Serum urate evaluation is a useful screening test best undertaken after recovery.

Identifiants

pubmed: 38150892
pii: S0960-8966(23)00808-8
doi: 10.1016/j.nmd.2023.11.012
pii:
doi:

Substances chimiques

Uric Acid 268B43MJ25
Glucose Transport Proteins, Facilitative 0
SLC2A9 protein, human 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

49-53

Subventions

Organisme : Medical Research Council
ID : MR/S01165X/1
Pays : United Kingdom

Informations de copyright

Copyright © 2023. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare no conflicts of interest.

Auteurs

Ros Quinlivan (R)

MRC Centre for Neuromuscular Disease, UCL Institute of Neurology, National Hospital for Neurology and Neurosurgery, London, UK. Electronic address: r.quinlivan@ucl.ac.uk.

Elaine Murphy (E)

Charles Dent Metabolic Unit, National Hospital for Neurology and Neurosurgery, Queen Square London, UK.

Shpresa Pula (S)

MRC Centre for Neuromuscular Disease, UCL Institute of Neurology, National Hospital for Neurology and Neurosurgery, London, UK.

Alexandra Pain (A)

Department of Acute and General Medicine, Stoke Mandeville Hospital, Mandeville Road, Aylesbury UK.

Henrietta Brain (H)

Department of Acute and General Medicine, Stoke Mandeville Hospital, Mandeville Road, Aylesbury UK.

Grace Scopes (G)

University of Buckingham, Stoke Mandeville, Aylesbury, UK.

Frenki Gjika (F)

University of Buckingham, Stoke Mandeville, Aylesbury, UK.

Naim Ahmadouk (N)

Department of Acute and General Medicine, Stoke Mandeville Hospital, Mandeville Road, Aylesbury UK.

Andreea Manole (A)

Department of neurogenetics, UCL Institute of Neurology, National hospital for Neurology and Neurosurgery, UK.

Henry Houlden (H)

Department of neurogenetics, UCL Institute of Neurology, National hospital for Neurology and Neurosurgery, UK.

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Classifications MeSH