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Failure to respond to treatment with typical antipsychotics is not associated with CYP2D6 ultrarapid hydroxylation
Author(s) -
Aitchison Katherine J.,
Munro Janet,
Wright Padraig,
Smith Shulabade,
Makoff Andrew J.,
Sachse Christoph,
Sham Pak C.,
Murray Robin M.,
Collier David A.,
Kerwin Robert W.
Publication year - 1999
Publication title -
british journal of clinical pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.216
H-Index - 146
eISSN - 1365-2125
pISSN - 0306-5251
DOI - 10.1046/j.1365-2125.1999.00006.x
Subject(s) - cyp2d6 , pharmacogenetics , genotyping , gene duplication , pharmacogenomics , allele , genotype , medicine , pharmacology , biology , genetics , gene
Aims To investigate whether or not there is a correlation between failure to respond to typical antipsychotics and CYP2D6 ultrarapid metaboliser status.Methods CYP2D6 phenotype (metaboliser status) was assigned following genotyping for gene duplication, as well as for the CYP2D6*3, CYP2D6*4, and CYP2D6*5 null alleles in 235 treatment‐refractory patients and 73 nonrefractory patients.Results Four (1.7%) of the 235 treatment‐refractory subjects were positive on the duplication assay, but, of these, two were found to represent duplications of a null allele (CYP2D6*4 ), therefore leaving only two (0.85%) positive for duplication of a wild type allele (ultrarapid metabolisers). Three (4.1%) of the nonrefractory subjects had a genotype consistent with ultrarapid metaboliser status. Fisher’s exact test gave a two‐tailed P value of 0.091, i.e. a trend towards an excess of ultrarapid metabolisers in the nonrefractory group, which was in the opposite direction to that predicted by our hypothesis.Conclusions Although the results show a trend towards an excess of ultrarapid metabolisers in the nonrefractory group, the percentages in the two groups of patients are both within the range for ultrarapid metabolisers in Caucasian populations. Our data are not consistent with ultrarapid metaboliser status being a major cause of failure to respond to typical antipsychotics.