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Letters to the Editor |
1 Hormone Laboratory, Aker University Hospital, 0514 Oslo, Norway
aAuthor for correspondence. Fax 47-22-158796; e-mail p.a.torjesen@ioks.uio.no.
| The first 20% of the full text of this article appears below. |
To the Editor:
Taieb et al. (1) in their recent report in Clinical Chemistry described the relationship of serum testosterone concentrations measured by 10 immunoassays and by isotope-dilution gas chromatographymass spectrometry (ID/GC-MS). Automated immunoassays fared badly, but RIAs agreed well with the ID/GC-MS.
In contrast to our findings, Taieb et al. (1) reported, in women, increased serum testosterone as assayed in the AutoDelfia immunoassay system (Perkin-Elmer). Between November 1, 2002, and February 28, 2003, we found for 2057 women a mean (median) testosterone of 2.1 (1.6) nmol/L by AutoDelfia, similar to the values of 1.7 (1.4) nmol/L for 2180 different female samples assayed consecutively in our routine using the Orion Diagnostica RIA between November 1, 2001, and February 28, 2002. By contrast, Taieb et al. (1) reported mean concentrations of
5 nmol/L in the female samples measured by the AutoDelfia.
In the same time periods, consecutive male samples had mean (median) values of 16.7 (14.8) nmol/L by AutoDelfia (n = 1447) and 13.9 (12.9) nmol/L by the Orion (n = 1505). Again, the difference between the automated
Unit of Hormonal Biochemistry, St. Louis Hospital, Assistance-Publique-Hôpitaux de Paris, 1 Avenue Claude Vellefaux, 75010 Paris, France
aAuthor for correspondence. Fax 33-1-4249-4280; e-mail philippe.boudou@sls.ap-hop-paris.fr.
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