S. Donohoe et al., Maternal cardiolipin, beta(2)-glycoprotein-I and prothrombin antibody expression in high-risk pregnancies with bilateral abnormal uterine artery Doppler waveforms, ULTRASOUN O, 13(5), 1999, pp. 317-322
Objective To compare the frequency of maternal serum antiphospholipid antib
odies (to cardiolipin, beta(2)-glycoprotein I and prothrombin) in pregnanci
es presenting with bilateral abnormal uterine artery Doppler waveforms.
Design Retrospective analysis of stored serum.
Subjects Cases comprised 47 singleton pregnancies with bilateral abnormal u
terine artery Doppler waveforms at 24 weeks of gestation, followed from 20
weeks, and controls were 100 healthy pregnancies with normal uterine artery
Doppler waveforms.
Methods Ultrasound examination utilized a 5-MHz curvi-linear transabdominal
transducer with pulsed and color Doppler facilities. Antiphospholipid anti
bodies were analyzed by ELISA methodology, and reference ranges were establ
ished using the geometric mean +/-2 SD of healthy non-pregnant adults. Huma
n chorionic gonadotropin (hCG) levels were obtained from patient notes.
Results Anticardiolipin antibodies were detected in 11 (23%) of the cases (
IgG, n = 7; IgM, n = 6) compared with ten (10%) of the controls (p < 0.05).
Low titer anticardiolipin IgG (range, 5.5-35.3; median, 6.3 GPL units) and
anticardiolipin IgM (range, 3.4-14.7; median, 5.3 MPL units) were detected
in cases. Amongst the cases, adverse perinatal outcomes were more common i
n the presence of raised levels of anticardiolipin antibodies. Anti-beta(2)
-glycoprotein I IgG was not detected in any of the cases. Antiprothrombin I
gG was not detected, but antiprothrombin IgM occurred in 10.6% of cases com
pared with 2% of controls.
Conclusions Women with persistent bilateral abnormal uterine artery Doppler
waveforms in mid-gestation were more likely to express raised levels of an
ticardiolipin antibodies than healthy controls with normal uteroplacental p
erfusion. Anticardiolipin antibodies without anti-beta(2)-glycoprotein I bi
nding may be involved in the pathogenesis of uteroplacental ischemia in a p
roportion of high-risk pregnancies.