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Articles |
1-Protease Inhibitor in Serum
Departments of
1
Clinical Chemistry,
2
Urology, and
3
Pathology, Helsinki University Central Hospital, FIN-00290 Helsinki, Finland.
a Author for correspondence. Fax 00358-09-4714804; e-mail ulf-hakan.stenman{at}huch.fi
Background: Prostate-specific antigen (PSA) occurs in serum both
free and in complex with protease inhibitors. The complex with
1-antichymotrypsin (ACT) is the major form in
serum, and the proportion of PSA-ACT is higher in prostate cancer (PCa)
than in benign prostatic hyperplasia (BPH). PSA also forms a complex
with
1-protease inhibitor (API) in vitro, and the
PSA-ACT complex has been detected in serum from patients with prostate
cancer. The aim of the present study was to develop a quantitative
method for the determination of PSA-API and to determine the serum
concentrations in patients with PCa and BPH.
Methods: The assay for PSA-API utilizes a monoclonal antibody to PSA as capture and a polyclonal antibody to API labeled with a Eu-chelate as a tracer. For calibrators, PSA-API formed in vitro was used. Serum samples were obtained before treatment from 82 patients with PCa, from 66 patients with BPH, and from 22 healthy females.
Results: The concentrations of PSA-API are proportional to the concentrations of total PSA. PSA-API comprises 1.07.9% (median, 2.4%) of total immunoreactive PSA in PCa and 1.312.2% (median, 3.6%) in BPH patients with serum PSA concentrations >4 µg/L. In patients with 420 µg/L total PSA, the proportion of PSA-API serum is significantly higher in BPH (median, 4.1%) than in PCa (median, 3.2%; P = 0.02).
Conclusions: The proportion of PSA-API in serum is lower in patients with PCa than in those with BPH. These results suggest that PSA-API is a potential adjunct to total and free PSA in the diagnosis of prostate cancer.© 1999 American Association for Clinical Chemistry
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