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Cytochrome P450 2D6 genotype does
not predict SSRI (fluoxetine or paroxetine) induced
hyponatraemia.
Stedman CA, Begg EJ, Kennedy MA,
Roberts R, Wilkinson TJ.
Department of Clinical Pharmacology,
Christchurch Hospital, Christchurch School of Medicine, Christchurch,
New Zealand.
AIMS: The aims of this study were to determine if
patients with SSRI-related hyponatraemia were (1) genetically poor
metabolizers of CYP2D6, and/or (2) had excessive plasma concentrations
of the SSRI antidepressant. METHODS: Plasma DNA from 20 people with
hyponatraemia attributable to fluoxetine or paroxetine was analysed for
the CYP2D6 alleles *1-*16. Trough plasma concentrations of fluoxetine
and norfluoxetine, or paroxetine were assayed in nine people who
remained on the antidepressant. RESULTS: Genotype results were compared
with those published in a large population study. The poor metabolizer
PM/PM genotype was present in one subject only, or 5% of the study
population, compared with 7.2% of a general population. The 95% Cl of
this result was 0-21%, suggesting that it is most unlikely that
hyponatremia is related to the PM/PM genotype. The intermediate IM/PM
genotype was present in 5% compared with 19.7% of a general population.
All differences were not statistically significant. Antidepressant
concentrations of fluoxetine (n = 5, all EM) and paroxetine (n = 1 IM/PM
and n = 3 EM) were all within the lower half of the reference range.
CONCLUSIONS: These results do not support the hypothesis that
SSRI-related hyponatraemia is linked to genetically poor metabolizers,
or excessive drug concentrations. Copyright 2002 John Wiley & Sons,
Ltd.
Publication Types:
PMID: 12404686 [PubMed - indexed for
MEDLINE]
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