Steroid hormone profiles in reproductive age patients with advanced endometriosis


Cite item

Full Text

Open Access Open Access
Restricted Access Access granted
Restricted Access Subscription or Fee Access

Abstract

Introduction. Investigating pathological changes in endogenous steroidogenesis associated with advanced extragenital endometriosis (AEGE) requires high-precision and sensitive methods. Aim. To investigate blood steroidome changes in AEGE. Materials and methods. Patients with AEGE and control subjects were tested for serum hormones using high-performance liquid chromatography-mass spectrometry (HPLC-MS). Results. Patients with AEGE had significant changes in the concentration of 9 steroids. Blood hormone concentrations in patients with and without AEGE were as follows: estradiol 0.18 vs. 0.12 ng/ml (p=0.05), 17-OH-progesterone0.55vs. 0.44ng/ml(p=0.05), testosterone0.81 vs. 0.43ng/ml(p<0.01), dihydrotestosterone- 0.16 vs. 0.37 ng/ml (p<0.1), dehydroepiandrosterone 3.56 vs. 5.98 ng/ml (p<0.01), DHEA sulfate 2533.00 vs. 4425.00 ng/ml (p<0.01), androstenedione 1.35 vs. 1.31 ng/ml (p=0.29), cortisol 164.00 vs. 90.50 ng/ml (p<0.01), corticosterone 4.87 vs. 1.20 ng/ml (p<0.01), 11-deoxycorticosterone 0.87 vs. 0.37 ng/ml (p<0.01). Progesterone concentrations were below the detection limit in both groups. Four logistic regression models allowed differentiation of blood steroidome of AEGE patients from that in controls. Conclusion. Endometriotic cysts in stage III - IVAEGE have no significant effect on changes in the steroidome. HPLC-MS differences in blood steroidome allow differentiation of patients with AEGE from control subjects.

Full Text

Restricted Access

About the authors

Stanislav V. Pavlovich

V.I. Kulakov National Medical Research Center for Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia; I.M. Sechenov First Moscow State Medical University, Ministry of Health of Russia (Sechenov University)

Email: s_pavlovich@oparina4.ru
MD, Academic Secretary

Mariia V. Iurova

V.I. Kulakov National Medical Research Center for Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia; I.M. Sechenov First Moscow State Medical University, Ministry of Health of Russia (Sechenov University)

Email: m_yurova@oparina4.ru
Specialist

Vitaliy V. Chagovets

V.I. Kulakov National Medical Research Center for Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia

Email: vvchagovets@gmail.com
Ph.D., Senior Researcher at the Laboratory of Proteomics and Metabolomics in Human Reproduction, Department of System Biology

Vladimir E. Frankevich

V.I. Kulakov National Medical Research Center for Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia

Email: v_frankevich@oparina4.ru
Ph.D., Head of Department of System Biology in Reproduction

Nataliya L. Starodubtseva

V.I. Kulakov National Medical Research Center for Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia

Email: n_starodubtseva@oparina4.ru
Ph.D., Head of Laboratory of Proteomics of Human Reproduction

V. D Chuprynin

V.I. Kulakov National Medical Research Center for Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia

Email: v_chuprynin@oparina4.ru

Gennady T. Sukhikh

V.I. Kulakov National Medical Research Center for Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia; I.M. Sechenov First Moscow State Medical University, Ministry of Health of Russia (Sechenov University)

Email: g_sukhikh@oparina4.ru
MD, Academician of the Russian Academy of Sciences, Director

References

  1. Chapron C., Marcellin L., Borghese B., Santulli P. Rethinking mechanisms, diagnosis and management of endometriosis. Nat. Rev. Endocrinol. 2019; 15(11): 666-82. https://dx.doi.org/10.1038/s41574-019-0245-z.
  2. Schenken R.S., Barbieri R.L., Eckler K. Endometriosis: pathogenesis, clinical features, and diagnosis. UpToDate. 2019. Available at: https://www.uptodate. com/contents/endometriosis-pathogenesis-clinical-features-and-diagnosis
  3. Zondervan K.T., Becker C.M., Missmer S.A. Endometriosis. N. Engl. J. Med. 2020; 382(13): 1244-56. https://dx.doi.org/10.1056/NEJMra1810764.
  4. Kalogera E., Pistos C., Provatopoulou X., Christophi C.A., Zografos G.C., Stefanidou M. et al. Bioanalytical LC-MS method for the quantification of plasma androgens and androgen glucuronides in breast cancer. J. Chromatogr. Sci. 2016; 54(4): 583-92. https://dx.doi.org/10.1093/chromsci/bmv190.
  5. Vercellini P., Somigliana E., Vigano P., Abbiati A., Barbara G., Fedele L. et al. “Blood on the tracks” from corpora lutea to endometriomas. BJOG. 2009; 116(3): 366-71. https://dx.doi.org/ 10.1111/j.1471-0528.2008.02055.x.
  6. Appendix: the revised AFS classification of endometriosis. In: Timmerman D., Deprest J., Bourne T. Ultrasound and endoscopic surgery in obstetrics and gynecology. A combined approach to diagnosis and treatment. London: Springer-Verlag; 2003: 216-7.
  7. Hakkinen M.R., Heinosalo T., Saarinen N., Linnanen T., Voutilainen R., Lakka T. et al. Analysis by LC-MS/MS of endogenous steroids from human serum, plasma, endometrium and endometriotic tissue. J. Pharm. Biomed. Anal. 2018; 152: 165-72. https://dx.doi.org/10.1016/j.jpba.2018.01.034.
  8. Palermo A., Botre F., de la Torre X., Zamboni N. Non-targeted LC-MS based metabolomics analysis of the urinary steroidal profile. Anal. Chim. Acta. 2017; 964: 112-22. https://dx.doi.org/ 10.1016/j.aca.2017.01.055.
  9. Higashi T., Ogawa S. Chemical derivatization for enhancing sensitivity during LC/ESI-MS/MS quantification of steroids in biological samples: a review. J. Steroid Biochem. Mol. Biol. 2016; 162: 57-69. https://dx.doi.org/10.1016/j. jsbmb.2015.10.003.
  10. Fulop I., Vari C.E., Miklos A., Imre S. LC-MS/MS ESI methods for the determination of oestrogens and androgens in biological matrix - a minireview. Farmacia. 2017; 65(4): 485-93.
  11. Jeanneret F., Tonoli D., Rossier M.F., Saugy M., Boccard J., Rudaz S. Evaluation of steroidomics by liquid chromatography hyphenated to mass spectrometry as a powerful analytical strategy for measuring human steroid perturbations. J. Chromatogr. A. 2016; 1430: 97-112. https://dx.doi.org/ 10.1016/j. chroma.2015.07.008.
  12. Yilmaz B.D., Bulun S.E. Endometriosis and nuclear receptors. Hum. Reprod. Update. 2019. 25(4): 473-85.https://dx.doi.org/10.1093/humupd/dmz005.
  13. Reis F.M., Petraglia F., Taylor R.N. Endometriosis: hormone regulation and clinical consequences of chemotaxis and apoptosis. Hum. Reprod. Update. 2013; 19(4): 406-18. https://dx.doi.org/10.1093/humupd/dmt010.
  14. Qi Q.M., Guo S.W., Liu X.S. Estrogen biosynthesis and its regulation in endometriosis. Reprod. Dev. Med. 2017; 1(1): 55-61. https://dx.doi. org/10.4103/2096-2924.210698.
  15. Huhtinen K., Saloniemi-Heinonen T., Keski-Rahkonen P., Desai R., Laajala D., Stahle M. et al. Intra-tissue steroid profiling indicates differential progesterone and testosterone metabolism in the endometrium and endometriosis lesions. J. Clin. Endocrinol. Metab. 2014; 99(11): E2188-97. https://dx.doi.org/10.1210/ jc.2014-1913.
  16. Attar E., Bulun S.E. Endometriosis. In: Fazlebas A., ed. Endometrium. 2nd ed. Taylor and Francis Book Ltd.; 2008: 691-710.
  17. Labrie F. Intracrinology. Mol. Cell. Endocrinol. 1991; 78(3): C113-8. https:// dx.doi.org/10.1016/0303-7207(91)90116-a.
  18. Gibson D.A., Simitsidellis I., Collins F., Saunders P.T.K. Endometrial intracrinology: oestrogens, androgens and endometrial disorders. Int. J. Mol. Sci. 2018; 19(10): 3276. https://dx.doi.org/ 10.3390/ijms19103276.
  19. Kalogera E., Pistos C., Provatopoulou X., Athanaselis S., Spiliopoulou C., Gounaris A. Androgen glucuronides analysis by liquid chromatography tandem-mass spectrometry: could it raise new perspectives in the diagnostic field of hormone-dependent malignancies? J. Chromatogr. B Analyt. Technol. Biomed. Life Sci. 2013; 940: 24-34. https://dx.doi.org/10.1016/j.jchromb.2013.09.022.

Supplementary files

Supplementary Files
Action
1. JATS XML

This website uses cookies

You consent to our cookies if you continue to use our website.

About Cookies