La. Cole et al., SELECTING HUMAN CHORIONIC-GONADOTROPIN IMMUNOASSAYS - CONSIDERATION OF CROSS-REACTING MOLECULES IN 1ST-TRIMESTER PREGNANCY SERUM AND URINE, American journal of obstetrics and gynecology, 168(5), 1993, pp. 1580-1586
OBJECTIVE: We investigated the variation in human chorionic gonadotrop
in results found with different commercial kits. Levels of human chori
onic gonadotropin and related molecules were determined in pregnancy s
erum and urine and compared with the specificities of different labora
tory, office, and home test kits. STUDY DESIGN: Total human chorionic
gonadotropin (nicked + nonnicked), nonnicked human chorionic gonadotro
pin, free beta subunit, and beta core fragment were measured in 242 se
rum samples and 125 urine samples from early pregnancies. RESULTS: In
serum, in the 2 weeks after the missed period when most pregnancy test
s are performed, median levels of total, nonnicked, and beta human cho
rionic gonadotropin (total + free beta + beta core) were similar (less
-than-or-equal-to 12% difference). Individual values, however, varied
significantly. For nonnicked human chorionic gonadotropin, values rang
ed from 41% to 145% and for beta from 101% to 145% of the total human
chorionic gonadotropin level. In urine individual nonnicked values var
ied from < 1% to 148% and beta values from 102% to 547% of the total h
uman chorionic gonadotropin level. A survey of 29 kits revealed that 1
0 were types detecting total human chorionic gonadotropin, five detect
ing nonnicked only, and 14 were beta assays. CONCLUSIONS: Results from
total, nonnicked, and beta human chorionic gonadotropin kits are not
necessarily interconvertible. Individual variations in levels of nicke
d human chorionic gonadotropin, free and beta core, and differences in
their recognition by immunoassays causes discordant results.