OBJECTIVE: This study was designed to determine whether the late lutea
l functional status of the corpora lutea in in vitro fertilization cyc
les alters the secretion of relaxin during pregnancy. STUDY DESIGN: An
alysis of serum relaxin, human chorionic gonadotropin, and steroid con
centrations in sera of women with pregnancies viable beyond the twelft
h week as a result of in vitro fertilization treatment was performed.
RESULTS: The serum estradiol and progesterone concentrations decreased
5.5- and 4-fold from days 5 to 6 after human chorionic gonadotropin t
o days 11 to 13 after human chorionic gonadotropin, respectively The s
erum relaxin concentration increased 8-fold between the 11- to 15-day
interval and the 16- to 50-day interval after human chorionic gonadotr
opin and another 6-fold to the 51- to 90-day interval after human chor
ionic gonadotropin (all p < 0.01). Multiple linear regression analysis
showed that the serum estradiol level 11 to 13 days after human chori
onic gonadotropin and the serum human chorionic gonadotropin level 11
to 15 days after human chorionic gonadotropin were the most powerful p
aired predictors of the concentration of serum relaxin measured in the
11- to 15-day interval after human chorionic gonadotropin interval (R
(2)=0.39, n=50), the 16- to 50-day interval (R(2)-0.61, n=51), and the
51- to SD-day interval (R(2)=0.55, n=39). CONCLUSION: Secretion of re
laxin is determined by an interaction of the late luteal functional st
atus of the corpora lutea and the human chorionic gonadotropin secrete
d by the implanting pregnancy. These data allow for the hypothesis tha
t inducing functional luteolysis by substituting one or more injection
s of luteinizing hormone for the human chorionic gonadotropin injectio
n may decrease secretion of steroids, relaxin, and other factors from
the corpora lutea during pregnancy, decreasing the risk of premature d
elivery in multiple gestations and the ovarian hyperstimulation syndro
me.