Association between maternal circulating IL-27 levels and preeclampsia
•We measured serum IL-27 level in normal pregnancy, preeclampsia and health nonpregnant women.•Serum IL-27 levels were elevated in healthy pregnant and preeclamptic groups.•A significant difference of IL-27 serum level was observed in preeclamptic group.•Serum IL-27 was considerably elevated in seve...
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Veröffentlicht in: | Cytokine (Philadelphia, Pa.) Pa.), 2018-02, Vol.102, p.163-167 |
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Sprache: | eng |
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Zusammenfassung: | •We measured serum IL-27 level in normal pregnancy, preeclampsia and health nonpregnant women.•Serum IL-27 levels were elevated in healthy pregnant and preeclamptic groups.•A significant difference of IL-27 serum level was observed in preeclamptic group.•Serum IL-27 was considerably elevated in severe preeclampsia, but not mild preeclampsia.•IL-27 serum levels were significantly differences in early onset and late onset sever preeclampsia.
In this study, we investigated the relationship between serum level of IL-27 with preeclampsia and its severity. Fifty-six preeclamptic, 21 health pregnant and 20 health nonpregnant women formed the study group. The levels of IL-27 in maternal circulation were determined by ELISA. IL-27 serum levels were found to be elevated in healthy pregnant and preeclamptic groups as compared to non-pregnant women, this increase was significant in preeclamptic cases (p=0.0004). Moreover, a significant difference of IL-27 serum level was observed between groups and the healthy pregnant controls, (p=0.0095). Notably, the level of IL-27 was considerably elevated in women with severe preeclampsia, but not with mild preeclampsia as compared with healthy pregnant women (p=0.0056, p=0.0964, respectively). Furthermore, IL-27 serum levels were significantly differences in early onset and late onset sever preeclampsia than in gestation matched healthy pregnancies (p=0.0376, p=0.0085, respectively). In conclusion, our results suggest IL-27 might be a useful biomarker for disease severity in preeclampsia. |
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ISSN: | 1043-4666 1096-0023 |
DOI: | 10.1016/j.cyto.2017.08.012 |