Effect of cabergoline on vascular permeability markers with the risk of ovarian hyperstimulation syndrome


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Resumo

The ovarian hyperstimulation syndrome (OHSS) results from enhanced vascular permeability, from activated endothelial vascular growth factor (VEGF). The selective dopamine receptor type 2 agonist cabergoline inactivates VEGF receptor 2 (VEGFR2), by blocking the further functions of VEGF, and prevents higher vascular permeability. Objective. To evaluate the effect of cabergoline on vascular permeability markers (VEGF, VEGF receptor 1 (VEGFR1), and VEGFR2 in the serum of women at risk for OHSS. Subject and methods. One hundred and sixty-eight women included in the IVF program were examined. Group 1 included 65 women at risk for OHSS who were given, for the prevention of this condition, oral cabergoline in a daily dose of 0.5 mg on the following day after transvaginal puncture for 5 days before the embryo transfer (ET) day. Group 2 consisted of 63 similar patients who did not take the drug. According to the development of OHSS, the patients were divided into subgroups: 1a (n = 38) and 2a (n = 30) without the syndrome being developed; 1b (n = 7) and 2b (n = 15) with OHSS. Group 3 comprised 40 women who had no risk factors OHSS (a control group). ELISA was used to measure the serum levels of VEGF, VEGFR1, and VEGFR2 in 90 high-risk patients and 40 control women. Results. On day 5 after cabergoline intake, Subgroup 1a women were found to have higher levels of soluble forms of VEGFR1 (p < 0.0007) and VEGFR2 (p < 0.0049) than the patients who did not take the drug. By the ET day, the OHSS subgroups versus the non-OHSS ones demonstrated a manifestation of the syndrome with lower VEGF1 and VEGF2 levels (p < 0.05). The administration of cabergoline could reduce the absolute risk of OHSS by 19% (95% confidence interval, 5-33%). Conclusion. The preventive effect of the selective dopamine receptor type 2 agonist cabergoline in the women at risk for OHSS shows itself as an increase in the serum levels of soluble VEGF1 and VEGF2 forms, which favors the optimal balance between these indicators and the maintenance of the physiological mechanism for vascular permeability.

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Sobre autores

S. Fetisova

Academician V.I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health of Russia

Email: svfetisova@mail.ru
postgraduate student at the 1st gynecological department

I. Korneeva

Academician V.I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health of Russia

Email: irina.korneeva@inbox.ru
MD, leading researcher, doctor of the highest category, 1st gynecological department

T. Saroyan

Academician V.I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health of Russia

Email: tata-l976@mail.ru
PhD, researcher at the 1st gynecological department

L. Krechetova

Academician V.I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health of Russia

Email: k_l_v_@mail.ru
PhD, head of the Laboratory of Clinical Immunology

L. Podrez

Academician V.I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health of Russia

Email: mylude@rambler.ru
doctor, laboratory of clinical immunology

Bibliografia

  1. Delvigne A., Rozenberg S. Epidemiology and prevention of ovarian hyperstimulation syndrome (ohss): a review. Hum. Reprod. Update. 2002; 8: 559-77.
  2. Soares S.R. Etiology of OHSS and use of dopamine agonists. Fertil. Steril. 2012; 97(3): 517-22.
  3. Gomez R., Simon C., Remohi J., Pellicer A. Administration of moderate and high doses of gonadotrophins to female rats increases ovarian vascular endothelial growth factor (VEGF) and VEGF receptor-2 expression that is associated to vascular hyperpermeability. Biol. Reprod. 2003; 68: 2164-71.
  4. Ferrara N., Kerbel R.S. Angiogenesis as a therapeutic target. Nature. 2005; 438: 967-74.
  5. Gille H., Kowalski J., Li B., Le Couter J., Moffat B., Zioncheck T.F. et al. Analysis of biological effects and signaling properties of Flt-1 (VEGFR-1) and KDR (VEGFR-2). A reassessment using novel receptor-specific vascular endothelial growth factor mutants. J. Biol. Chem. 2001; 276(5): 3222-30.
  6. Soares S.R., Gomez R., Simon С. Targeting the vascular endothelial growth factor system to prevent ovarian hyperstimulation syndrome. Hum. Reprod. Update. 2008; 14(4): 321-33.
  7. Papaleo E., Doldi N., De Santis L., Marelli G., Marsiglio E., Rofena S., Ferrari A. Cabergoline influences ovarian stimulation in hyperprolactinaemic patients with polycystic ovary syndrome. Hum. Reprod. 2001; 16(11): 2263-6.
  8. Pau E. Plasma levels of soluble vascular endothelial growth factor receptor-1 may determine the onset of early and late ovarian hyperstimulation syndrome. Hum. Reprod. 2006; 21(6): 1453-60.
  9. Pietrowski D. Ovarian hyperstimulation syndrome is correlated with a reduction of soluble VEGF receptor protein level and a higher amount of VEGF-A. Hum. Reprod. 2012; 27(1): 196-9.

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