F. Barbe et al., UNDETECTABLE LUTEINIZING-HORMONE LEVELS USING A MONOCLONAL IMMUNOMETRIC ASSAY, Journal of endocrinological investigation, 18(10), 1995, pp. 806-808
Previous studies have shown wide discrepancies among the results obtai
ned with different immunometric assays. We present five cases (out of
4000 women) whose plasma luteinizing hormone was not detected using a
LH immunometric assay (LH Stratus Baxter) but was recognized by other
kits. These cases concerned one 28-year-old woman presenting with infe
rtility and four postmenopausal women. The LH Amerlite kit gave detect
able but low results. The results obtained with the other kits were >7
IU/l. FSH levels were >7 IU/l. In one case, sera were taken before an
d after the menopause, differences between the LH results increased. D
iscrepancies among LH assays kits have been attributed to variation bo
th in standard curve calibration and in epitope specificity of the kit
monoclonal antibodies. The Baxter kit might misrecognize some isoform
s present in postmenopausal women. The present data illustrate the pot
ential false results with such immunoassays in routine clinical labora
tory testing. When undetectable LH results are not clinically explaine
d or when disparities between LH and FSH are observed, we suggest usin
g a second methodology or a bioassay if necessary. Improvement in LH a
ssays and standardization might resolve the problem of discrepancies b
etween the bH results.