Time-resolved immunofluorometric assay of sex-hormone binding globulin.

S Niemi, O Mäentausta, NJ Bolton… - Clinical …, 1988 - academic.oup.com
S Niemi, O Mäentausta, NJ Bolton, GL Hammond
Clinical chemistry, 1988academic.oup.com
A time-resolved immunofluorometric assay (trlFMA) for human sex-hormone binding
globulin (SHBG) is described in which antibody-coated tubes or microliter strip-wells and a
europium (Eu) chelate-labeled monoclonal antibody are used. The trlFMA sensitivity is
similar to that of other SHBG immunoassays, and other analytical variables compare
favorably with an SHBG immunoradiometric assay (IRMA) kit and a steroid binding capacity
assay: the interassay coefficient of variation (CV) is less than 8% and the intra-assay CV is …
Abstract
A time-resolved immunofluorometric assay (trlFMA) for human sex-hormone binding globulin (SHBG) is described in which antibody-coated tubes or microliter strip-wells and a europium (Eu) chelate-labeled monoclonal antibody are used. The trlFMA sensitivity is similar to that of other SHBG immunoassays, and other analytical variables compare favorably with an SHBG immunoradiometric assay (IRMA) kit and a steroid binding capacity assay: the interassay coefficient of variation (CV) is less than 8% and the intra-assay CV is less than 6% for concentrations between 6 and 200 nmol/L. The reference intervals (means +/- SD) for SHBG concentrations (nmol/L) in serum from 10 men, 10 women, and 10 pregnant women were 23 +/- 12, 65 +/- 39, and 439 +/- 122, respectively. In 14 hirsute women the mean +/- SD serum SHBG concentration (37 +/- 21 nmol/L) was significantly lower (P less than 0.01) than the mean for an age-matched, nonhirsute female comparison group. The trlFMA is technically simple, requires no centrifugation or separation reagent, and takes a counting time of only 1 s. In addition, the Eu-label is nontoxic, presents no waste-disposal problems, and has a long shelf life.
Oxford University Press