Interleukin-22/Interleukin-22 binding protein axis and oral contraceptive use in polycystic ovary syndrome - PubMed (original) (raw)
Interleukin-22/Interleukin-22 binding protein axis and oral contraceptive use in polycystic ovary syndrome
Seren Aksun et al. Endocrine. 2023 Jul.
Abstract
Purpose: Polycystic ovary syndrome (PCOS) is associated with alterations in gut microbiota. The cytokine interleukin-22 (IL-22) is produced by immune cells and closely linked to gut immunity, which is tightly controlled by its binding protein (IL-22BP). In this study, we aimed to assess whether IL-22/IL-22BP axis is altered in PCOS at baseline and in response to short-term oral contraceptive (OC) therapy.
Methods: We have evaluated circulating concentrations of IL-22 and IL-22BP in serum samples of 63 PCOS patients and 39 age- and BMI-matched healthy controls. Blood samples were taken in the early follicular phase of a cycle and stored at -80 °C. Serum IL-22 and IL-22BP levels were measured by ELISA at baseline in both women with PCOS and controls, and after 3 months of OC use in PCOS group. IL-22/IL-22BP ratio was calculated in order to have a better reflection of IL-22 biological activity.
Results: At baseline, serum IL-22, IL-22BP concentrations and IL22/IL-22BP ratio were similar between women with PCOS and healthy controls. Three months of OC use along with general lifestyle advice resulted in a significant increase in IL-22/IL-22BP ratio in the PCOS group (62.4 [IQR:14.7-172.7] at baseline vs 73.8 [IQR:15.1-264.3] after OC use respectively p = 0.011).
Conclusions: Results of this study show that women with PCOS have similar circulating concentrations of IL-22 and IL-22BP with healthy women and that short term oral contraception is associated with an increase in IL-22/IL-22BP ratio suggesting higher biological activity of the IL-22 system with OC use in PCOS.
Keywords: IL-22; IL-22 binding protein; Microbiota; Oral contraceptive; Polycystic ovary syndrome.
© 2023. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
References
- B.O. Yildiz, G. Bozdag, Z. Yapici, I. Esinler, H. Yarali, Prevalence, phenotype and cardiometabolic risk of polycystic ovary syndrome under different diagnostic criteria. Hum. Reprod. 27(10), 3067–3073 (2012). https://doi.org/10.1093/humrep/des232 - DOI - PubMed
- R.C.E. Azziz, Z. Chen, A. Dunaif, J.S. Laven, R.S. Legro, D. Lizneva, B. Natterson-Horowtiz, H.J. Teede, B.O. Yildiz, Polycystic ovary syndrome. (2016). https://doi.org/10.1038/nrdp.2016.57
- G. Mammadova, C. Ozkul, S. Yilmaz Isikhan, A. Acikgoz, B.O. Yildiz, Characterization of gut microbiota in polycystic ovary syndrome: Findings from a lean population. Eur. J. Clin. Investig. 51(4), e13417 (2021). https://doi.org/10.1111/eci.13417 - DOI
- X. Qi, C. Yun, L. Sun, J. Xia, Q. Wu, Y. Wang et al. Gut microbiota-bile acid-interleukin-22 axis orchestrates polycystic ovary syndrome. Nat. Med. 25(8), 1225–1233 (2019). https://doi.org/10.1038/s41591-019-0509-0 - DOI - PubMed - PMC
- G. Conway, D. Dewailly, E. Diamanti-Kandarakis, H.F. Escobar-Morreale, S. Franks, A. Gambineri et al. The polycystic ovary syndrome: a position statement from the European Society of Endocrinology. Eur. J. Endocrinol. 171(4), P1–P29 (2014). https://doi.org/10.1530/eje-14-0253 - DOI - PubMed
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical