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Would it not be more appropriate to monitor the plasma fluoxetine levels
closely? A poor metaboliser will show increased levels, and the dose could
be adjusted accordingly? Would this be right?

David Gerrie



-----Original Message-----
From: Graham Mould [mailto:[log in to unmask]]
Sent: 22 October 2003 14:34
To: [log in to unmask]
Subject: Re: CYP2D6 and Prozac

you can measure the enzyme in a blood sample and so called genotype the
person.  A company called Genesolve, part of LGC is a company that tested
for that enzyme (CYP2D6) as well as the other cytochrome variants.  I think
LGC is at Teddington and Genesolve is a spin off from the University of
Dundee.  I think Chandos Clincial research in Park Royal, London also
measures it.  You could measure it whilst the pateint is taking the drug.
The analysis is (or was) expensive, and I don't think it's worth testing all
patients, in fact its not worth testing any patient really.  However the
question of whether one should 'metabolically' categorize patients into slow
or rapid (or intermediate) metabolisers is another debate.
Hope this is useful.
Graham Mould

-----Original Message-----
From: PETER HUDSON [mailto:[log in to unmask]]
Sent: 22 October 2003 10:33
To: [log in to unmask]
Subject: CYP2D6 and Prozac


Dear all

This morning, a patient on Prozac, presented her GP with a sheaf of
documents which she has obtained from the internet about the CYP2D6 enzyme.
This enzyme is involved in the metabolism of Fluoxetine.  Apparently 10% of
people have a low activity.  Poor metabolism of the drug by an individual
has resulted in legal action in the USA.  The patient has asked to be
tested.

Does anyone do this?
Is it possible to detect CYP2D6 phenotype when the patient is already taking
the drug?
The Gp also asks, if an assay is available, should he be testing all his
patients on Prozac?

Thanks

Peter Hudson

Peter Hudson
Principal Biochemist
Wrexham Maelor Hospital
Wales, UK. LL13 7TD
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