Q. Qiu et al., TOTAL URINARY FOLLICLE-STIMULATING-HORMONE AS A BIOMARKER FOR DETECTION OF EARLY-PREGNANCY AND PERIIMPLANTATION SPONTANEOUS-ABORTION, Environmental health perspectives, 105(8), 1997, pp. 862-866
Total concentrations of follicle stimulating hormone (FSH) were evalua
ted in daily urine samples from conceptive and nonconceptive menstrual
cycles by measurement of the FSH beta subunit following treatment of
the samples to dissociate the FSH heterodimer. Samples were self-colle
cted by normal subjects during cycles in which daily blood samples als
o were obtained. Daily blood and urine specimens were collected prospe
ctively from 10 subjects in conceptive cycles, which led to normal pre
gnancies, and from 10 subjects with bilateral tubal ligations to provi
de control samples from nonconceptive cycles. Mean serum and urinary F
SH concentration profiles were parallel in both groups following ovula
tion and during the first 9 days of the luteal phase. Mean values for
both serum and urinary FSH rose significantly above the postovulatory
baseline by 10-12 days following the midcycle luteinizing hormone (LH)
peak in nonconceptive cycles, but did not rise at any time following
ovulation during conceptive cycles. Following regression analysis of t
he changing FSH concentrations between days 9-14 post-LH surge in conc
eptive cycles, a slope of less than or equal to 0.02 ng FSH/mg creatin
ine/day was selected as a cutoff point to identify conceptive cycles.
There was a high concordance between the day of LH peak in serum and t
he day of FSH peak in urine. Therefore, in applying the algorithm, the
day of FSH peak in urine was used to determine the days for which the
FSH slope would be calculated, i.e., days 9-14 post-FSH peak in urine
. The sensitivity and specificity of the change in urinary FSH concent
rations to detect pregnancy in a different set of 55 cycles were found
to be 88.9% and 89.3%, respectively. All six cases of early fetal los
s in the sample set were correctly identified. These results suggest t
hat urinary FSH can be used as an additional biomarker for the verific
ation of early pregnancy in prospective epidemiologic studies in which
early fetal loss is a suspected outcome.