We sought to examine the relationship between excessive tumor necrosis fact
or-alpha (TNF-alpha) release las measured by sTNFp55 plasma concentrations)
and risk of eclampsia and preeclampsia, respectively, among sub-Saharan Af
rican women delivering at Harare Maternity Hospital, Zimbabwe. In total, 33
pregnant women with eclampsia, 138 women with preeclampsia and 185 normote
nsive women were included in a case-control study conducted during the peri
od, June 1995 through April 1996. Postpartum plasma sTNFp55 was measured by
enzyme linked immunosorbent assay. Women with eclampsia had significantly
higher sTNFp55 than normotensive controls (1.87 vs 1.35 ng/ml, P < 0.001).
Similarly, women with preeclampsia had sTNFp55 concentrations higher than n
ormotensive controls (1.69 vs 1.35 ng/ml, P < 0.001). The odds ratio for ec
lampsia was 5.00 (adjusted odds ratio (OR) 5.00, 95% confidence interval (C
I) 1.20-20.92) among women in the highest quartile of the control sTNFp55 d
istribution compared with women in the lowest quartile. The corresponding o
dds ratio and 95% CI for preeclampsia was 2.37 (1.11-5.06). Postpartum plas
ma sTNFp55 concentrations are increased among Zimbabwean women with eclamps
ia and preeclampsia as compared with their normotensive counterparts. These
findings are consistent with the hypothesized role of cytokines in mediati
ng endothelial dysfunction and the pathogenesis of preeclampsia/eclampsia.
Additional work is needed to identify modifiable risk factors for the exces
sive synthesis and release of TNF-c( in pregnancy; and to assess whether me
asurements of sTNFp55 early in pregnancy may be used to identify women like
ly to benefit from anti-inflammatory therapy. (C) 1998 Elsevier Science Ire
land Ltd. All rights reserved.