Associations between pre‐eclampsia and protein C and protein S levels among pregnant Nigerian women

Objective To evaluate levels of protein C and free protein S among women with pre‐eclampsia, and determine whether there is a relationship between deficiencies and pre‐eclampsia. Methods A cross‐sectional study was conducted at a hospital in Nigeria from July 2013 to March 2014 among 90 pregnant wom...

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Veröffentlicht in:International journal of gynecology and obstetrics 2017-04, Vol.137 (1), p.26-30
Hauptverfasser: Okoye, Helen C., Eweputanna, Lisa I., Okpani, Anthony O.U., Ejele, Oseikhuemen A.
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Sprache:eng
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Zusammenfassung:Objective To evaluate levels of protein C and free protein S among women with pre‐eclampsia, and determine whether there is a relationship between deficiencies and pre‐eclampsia. Methods A cross‐sectional study was conducted at a hospital in Nigeria from July 2013 to March 2014 among 90 pregnant women with pre‐eclampsia (blood pressure ≥140/90 mm Hg, proteinuria ≥300 mg in 24 hours) and 90 normotensive pregnant women (control group). Plasma levels of protein C and free protein S were analyzed by enzyme‐linked immunosorbent assay, and protein C activity by a chromogenic method. Results Mean protein C antigen and activity levels did not differ between groups (P=0.639 and P=0.444, respectively). The incidence of protein C antigen and activity deficiency also did not differ (P=0.288 and P>0.99, respectively). The mean free protein S antigen level was higher among women with pre‐eclampsia (54.48%±19.58%) than in the control group (47.23%±10.27%; P=0.004). No woman in the control group had protein S deficiency, as compared with 2 (2%) of the women with pre‐eclampsia (P=0.497). No association was found between deficiencies of these proteins and pre‐eclampsia. Conclusion Deficiencies of protein C and free protein S are unlikely to be etiopathogenetic for pre‐eclampsia; therefore, therapeutic intervention should focus on other potential pathogenetic pathways. Protein C and free protein S disorders are unlikely to be associated with pre‐eclampsia etiopathogenesis. Therapeutic intervention should focus on other potential pathogenetic pathways.
ISSN:0020-7292
1879-3479
DOI:10.1002/ijgo.12085