La. Norris et al., WHOLE-BLOOD PLATELET-AGGREGATION IN MODERATE AND SEVERE PREECLAMPSIA, British journal of obstetrics and gynaecology, 100(7), 1993, pp. 684-688
Objective To compare whole blood platelet aggregation in moderate and
severe pre-eclampsia with normal pregnancy. Design Whole blood platele
t aggregation in response to collagen, ADP, PAF, adrenalin and arachid
onic acid was measured in the pre-eclampsia group at 36 weeks gestatio
n and at 1, 24 and 48 h and at five days and six weeks post delivery.
The normal pregnancy group were studied serially at 12, 20, 28, 32, an
d 36 weeks gestation and at 1, 24, 48 h and six weeks post delivery. S
etting Trinity College Medical School, St James's Hospital, Dublin. Su
bjects Thirty women with diagnosed pre-eclampsia were recruited for th
e study. Fifteen of these women had severe pre-eclampsia and the remai
ning 15 had moderate disease. The pre-eclampsia group were compared wi
th 20 healthy primigravid women with uncomplicated pregnancies and del
iveries. Results In women with severe pre-eclampsia, platelet aggregat
ion in response to collagen, ADP, adrenalin and arachidonic acid was s
ignificantly lower at 36 weeks gestation compared with normal pregnanc
y. Lower levels of collagen induced aggregation were also found at 1 h
post delivery when compared with normal pregnancy. Women with moderat
e pre-eclampsia showed a decreased response to aggregating agents at 3
6 weeks gestation but this was not significant. ADP, collagen and PAF
induced aggregation was higher in women with moderate pre-eclampsia at
36 weeks gestation and during the early puerperium compared with seve
re pre-eclampsia. Conclusions The clinical signs of pre-eclampsia are
accompanied by a reduction in platelet responsiveness, the extent of w
hich is related to the severity of the disease. This suggests that an
abnormal platelet activation occurs early in pregnancies destined to b
e complicated by pre-eclampsia. This activation may be involved in the
pathogenesis of pre-eclampsia since its inhibition using low dose asp
irin has been shown to modify the disease in high risk pregnancies.