Re. Lieppman et al., AN ASSOCIATION BETWEEN ELEVATED LEVELS OF HUMAN CHORIONIC-GONADOTROPIN IN THE MIDTRIMESTER AND ADVERSE PREGNANCY OUTCOME, American journal of obstetrics and gynecology, 168(6), 1993, pp. 1852-1857
OBJECTIVE: Unexplained elevations in maternal serum alpha-fetoprotein
in the midtrimester are associated with adverse pregnancy outcome. Rec
ently it has also been suggested that elevations of maternal serum hum
an chorionic gonadotropin in the second trimester may be associated wi
th adverse pregnancy outcome. STUDY DESIGN: We conducted a cohort stud
y of 460 women at Swedish Medical Center, Seattle, Washington, between
Jan. 1, 1990, and Aug. 15, 1991, inclusive. Entry criteria for the co
hort included (1) triple screen analysis (maternal serum alpha-fetopro
tein, human chorionic gonadotropin, unconjugated estriol) between 15 a
nd 18 weeks' gestation, (2) a risk for Down syndrome of more than one
in 195 on the basis of triple screen analysis, (3) study group human c
horionic gonadotropin greater-than-or-equal-to 2 multiples of the medi
an and referent group less-than-or-equal-to 2 multiples of the median,
alpha-fetoprotein less-than-or-equal-to 2 multiples of the median, un
conjugated estriol greater-than-or-equal-to 0.5 multiples of the media
n, and (4) chromosomally normal single gestation without anomalies. Cu
mulative incidence risk ratios were estimated for each pregnancy outco
me as a measure of the relative association with elevated human chorio
nic gonadotropin (greater-than-or-equal-to 2.0 multiples of the median
) and adverse pregnancy outcome: low birth weight, less-than-or-equal-
to 2500 gm; preterm delivery, <37 weeks' gestation; and small for gest
ational age, less-than-or-equal-to 10th percentile. The Mantel extensi
on test was used to evaluate any apparent linear trend in risk between
level of human chorionic gonadotropin and adverse pregnancy outcome.
RESULTS: Elevated human chorionic gonadotropin levels were associated
with an increased risk for low birth weight (relative risk = 4.0), pre
term delivery (relative risk = 2.8), and small for gestational age (re
lative risk = 1.8). The risk for each adverse outcome increased with i
ncreasing levels of human chorionic gonadotropin. CONCLUSIONS: Elevati
ons of human chorionic gonadotropin in the midtrimester appear to be a
ssociated with adverse pregnancy outcome. The magnitude of the risk co
rrelates with the level of human chorionic gonadotropin. This risk app
ears to be independent of the risk for adverse pregnancy outcome assoc
iated with unexplained elevations of maternal serum alpha-fetoprotein.