Second-trimester maternal serum marker screening: Maternal serum alpha-fetoprotein, beta-human chorionic gonadotropin, estriol, and their various combinations as predictors of pregnancy outcome
Y. Yaron et al., Second-trimester maternal serum marker screening: Maternal serum alpha-fetoprotein, beta-human chorionic gonadotropin, estriol, and their various combinations as predictors of pregnancy outcome, AM J OBST G, 181(4), 1999, pp. 968-974
OBJECTIVE: We evaluated the value of all 3 common biochemical serum markers
, maternal serum alpha-fetoprotein. beta-human chorionic gonadotropin, and
unconjugated estriol, and combinations thereof as predictors of pregnancy o
utcome.
STUDY DESIGN: A total of 60,040 patients underwent maternal serum screening
. All patients had maternal serum alpha-fetoprotein measurements; beta-huma
n chorionic gonadotropin was measured in 45,565 patients, and 24,504 patien
ts had determination of all 3 markers, including unconjugated estriol. The
incidences of various pregnancy outcomes were evaluated according to the se
rum marker levels by using clinically applied cutoff
RESULTS: In confirmation of previous observations, increased maternal serum
alpha-fetoprotein levels (>2.5 multiples of the median) were found to be s
ignificantly associated with pregnancy-induced hypertension, miscarriage, p
reterm delivery, intrauterine growth restriction, intrauterine fetal death,
oligohydramnios, and abruptio placentae. Increased beta-human chorionic go
nadotropin levels (>2.5 multiples of the median [MoM]) were significantly a
ssociated with pregnancy-induced hypertension, miscarriage, preterm deliver
y, and intrauterine fetal death. Finally, decreased unconjugated estriol le
vels (<0.5 MoM) were found to be significantly associated with pregnancy-in
duced hypertension, miscarriage, intrauterine growth restriction, and intra
uterine fetal death. As with increased second-trimester maternal serum alph
a-fetoprotein levels, increased serum beta-human chorionic gonadotropin and
low unconjugated estriol levels are significantly associated with adverse
pregnancy outcomes. These are most likely attributed to placental dysfuncti
on.
CONCLUSION: Multiple-marker screening can be used not only for the detectio
n of fetal anomalies and aneuploidy but also for detection of high-risk pre
gnancies.