Can M-30, M-65, and IL-6 serum levels be useful markers in the diagnosis of preeclampsia and gestational diabetes?
A. Jafarzade, B. Bulut, H. Bulut, V. Mihmanli Department of Obstetrics and Gynecology, Koru Ankara Hospital, Ankara, Turkey. jafarzade_aytac@yahoo.com
OBJECTIVE: We aimed to evaluate the maternal and fetal serum M-30, M-65 and IL-6 levels in preeclampsia and gestational diabetes mellitus (GDM) in both maternal and cord blood.
PATIENTS AND METHODS: Women with preeclampsia (n=30), GDM (n=30), and uncomplicated pregnancy (n=28) were evaluated in a cross-sectional study. After clamping during delivery, the serum M-30, M-65, and IL-6 levels were measured in both maternal venous blood and cord blood.
RESULTS: The serum M-30, M-65, and IL-6 levels were significantly higher in preeclampsia and GDM patients’ maternal blood and cord blood samples compared to the control group. In the preeclampsia group, M-65 was significantly higher in cord blood compared with the level in maternal serum, but there was no significant difference between the GDM and control groups. The control group’s IL-6 level in cord blood was statistically significantly lower than the other groups. Although the M-30 value in both maternal and cord blood was statistically lower in the control group than in the GDM group, there was no significant difference between the two groups when compared to the preeclampsia group.
CONCLUSIONS: M-30 and M-65 molecules appear to have the potential to serve as biochemical markers in placental diseases, particularly preeclampsia and gestational diabetes. Due to the insufficient sample sizes, more research is needed.
Free PDF Download
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License
To cite this article
A. Jafarzade, B. Bulut, H. Bulut, V. Mihmanli
Can M-30, M-65, and IL-6 serum levels be useful markers in the diagnosis of preeclampsia and gestational diabetes?
Eur Rev Med Pharmacol Sci
Year: 2023
Vol. 27 - N. 12
Pages: 5795-5802
DOI: 10.26355/eurrev_202306_32818
Publication History
Published online: 27 Jun 2023