Literature DB >> 27333872

Epidemiology, pathophysiology and putative genetic basis of carbamazepine- and oxcarbazepine-induced hyponatremia.

B Berghuis1, G-J de Haan1, M P H van den Broek2, J W Sander1,3, D Lindhout1,4, B P C Koeleman4.   

Abstract

The use of carbamazepine (CBZ) and oxcarbazepine (OXC) as first-line antiepileptic drugs in the treatment of focal epilepsy is limited by hyponatremia, a known adverse effect. Hyponatremia occurs in up to half of people taking CBZ or OXC and, although often assumed to be asymptomatic, it can lead to symptoms ranging from unsteadiness and mild confusion to seizures and coma. Hyponatremia is probably due to the antidiuretic properties of CBZ and OXC that are, at least partly, explained by stimulation of the vasopressin 2 receptor/aquaporin 2 pathway. No known genetic risk variants for CBZ- and OXC-induced hyponatremia exist, but likely candidate genes are part of the vasopressin water reabsorption pathway.
© 2016 EAN.

Entities:  

Keywords:  antiepileptic drugs; drug treatment; epilepsy; sodium; vasopressin receptor 2

Mesh:

Substances:

Year:  2016        PMID: 27333872     DOI: 10.1111/ene.13069

Source DB:  PubMed          Journal:  Eur J Neurol        ISSN: 1351-5101            Impact factor:   6.089


  13 in total

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