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

Authors :
Berghuis, B.
Haan, G. ‐ J.
Broek, M. P. H.
Sander, J. W.
Lindhout, D.
Koeleman, B. P. C.
Source :
European Journal of Neurology; Sep2016, Vol. 23 Issue 9, p1393-1399, 7p
Publication Year :
2016

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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13515101
Volume :
23
Issue :
9
Database :
Complementary Index
Journal :
European Journal of Neurology
Publication Type :
Academic Journal
Accession number :
117483757
Full Text :
https://doi.org/10.1111/ene.13069