Objective: To investigate whether neutrophils and systemic complement are a
ctivated in pregnancies complicated by preeclampsia more than in normal pre
gnancies.
Methods: We measured native complement components and activation products i
n plasma by enzyme immunoassays in 19 women with uncomplicated pregnancies,
15 with preeclampsia before cesarean deliveries, and 16 nonpregnant women.
Neutrophil activation was measured by specific enzyme immunoassays for mye
loperoxidase and lactoferrin.
Results: Myeloperoxidase was significantly higher in women with preeclampsi
a (197 mug/L, 95% confidence interval [CI] 94, 646) than in women with unco
mplicated pregnancies (124 mug/L, 95% CI 70, 289; P = .009), whereas lactof
errin did not differ between groups. C4 was decreased in preeclamptic women
(0.16 g/L, 95% Cl 0.07, 0.48) compared with women with uncomplicated pregn
ancies (0.21, 95% CI 0.10, 0.30, P < .001). There were no differences for t
he other native complement components. There was a significant decrease in
C1rs-C1 inhibitor, 13 AU/mL (95% CI 9,34) versus 19 (95% CI 13, 38) (P <les
s than or equal to> .001) in normal pregnant women compared with nonpregnan
t women. There also was an increase in C3, C4, C9 (data not shown), C4bp, 1
32% (95% CI 94%, 161%) versus 91% (95% CI 57%, 128%); C3bc (7.4 AU/mL, 95%
CI. 4.2, 10.7) versus 4.8 AU/mL (95% CI 3.2, 7.3) and C4bc (8.6 AU/mL, 95%
CI 5.7, 14.0) versus 3.5 AU/mL (95% CI 2.2, 6.7) in normal pregnant women c
ompared with nonpregnant women (P less than or equal to .001).
Conclusion: Neutrophil activation in preeclampsia was shown by systemic inc
reases in myeloperoxidase. Except for a decrease in C4, systemic complement
activation could not be detected in preeclampsia. (C) 2001 by The American
College of Obstetricians and Gynecologists.