ISSN 0300-9092 (Print)
ISSN 2412-5679 (Online)

The incretin system and female reproductive function: receptor distribution, molecular mechanisms and new therapeutic prospects

Dora S.V., Khalimov Yu.Sh., Bezhenar V.F., Lisker A.V., Shvets Z.V., Volkova A.R., Kolyabina A.B., Murzina O.S.

Pavlov First Saint Petersburg State Medical University, Ministry of Health of Russia, St. Petersburg, Russia

The widespread use of glucagon-like peptide-1 (GLP-1) receptor agonists in the treatment of type 2 diabetes and obesity in women of reproductive age highlights the importance of investigating their potential impact on fertility. This review summarizes the current evidence on the role of the incretin system in the regulation of female reproductive function. The most convincing data obtained from patients with polycystic ovary syndrome (PCOS) demonstrate the ability of GLP-1 receptor agonists to reduce insulin resistance and hyperinsulinemia that can be associated with the restoration of a regular menstrual cycle, an increase in the frequency of ovulatory cycles and a higher likelihood of pregnancy. The effects on the reproductive system are due to both systemic improvement in metabolism and weight loss, and to direct action on tissues expressing GLP-1 receptors (the hypothalamic-pituitary axis, the ovaries and endometrium). Direct mechanisms include modulation of steroidogenesis, increased endometrial receptivity, and a reduction in inflammation and oxidative stress.
The safety of using GLP-1 receptor agonists during the periconceptional period remains a matter of debate. Despite data obtained from preclinical studies on potential embryotoxicity, available clinical observations have not revealed a statistically significant increase in the risk of congenital malformations following accidental exposure to the drug during the first trimester of pregnancy. Nevertheless, current guidelines recommend discontinuing treatment before conception.
Conclusion. To expand the clinical use of GLP-1 receptor agonists in gynecological and reproductive medicine, further research is needed to investigate their effectiveness in women without PCOS, to develop standardized protocols for periconceptional safety and to assess the potential of new generations of incretin-based drugs.

Authors’ contributions. Dora S.V., Khalimov Yu.Sh., Bezhenar V.F. – conception and design of the review; Lisker A.V., Shvets Z.V., Kolyabina A.B., Murzina O.S. – search and analysis of literary sources; Dora S.V., Shvets Z.V., Lisker A.V., Volkova A.R. – writing the text; Khalimov Yu.Sh., Bezhenar V.F., Volkova A.R. – editing and critical revision of the content; Dora S.V., 
Khalimov Yu.Sh., Bezhenar V.F., Lisker A.V., Shvets Z.V., Volkova A.R., Kolyabina A.B., Murzina O.S. – approval of the final version.
Conflicts of interest. Authors declare lack of the possible conflicts of interest.
Funding. The study was conducted without sponsorship.
Generative Artificial Intelligence. Artificial intelligence tools were not used in the preparation of this article.
For citation: Dora S.V., Khalimov Yu.Sh., Bezhenar V.F., Lisker A.V., Shvets Z.V., Volkova A.R., Kolyabina A.B., Murzina O.S. The incretin system and female reproductive function: receptor distribution, 
molecular mechanisms and new therapeutic prospects.
Akusherstvo i Ginekologiya/Obstetrics and Gynecology. 2026; (6): 39-46 (in Russian)
https://dx.doi.org/10.18565/aig.2025.272

Keywords

glucagon-like peptide-1 receptor agonists
semaglutide
liraglutide
fertility
infertility
menstrual cycle
polycystic ovary syndrome
insulin resistance
obesity
diabetes mellitus
steroidogenesis
endometrial receptivity
periconceptional period

References

  1. Lee J.M., Sharifi M., Oshman L., Griauzde D.H., Chua K.P. Dispensing of glucagon-like peptide-1 receptor agonists to adolescents and young adults, 2020-2023. JAMA. 2024; 331(23): 2041-43. https://dx.doi.org/10.1001/jama.2024.7112
  2. Zhou L., Qu H., Yang L., Shou L. Effects of GLP1RAs on pregnancy rate and menstrual cyclicity in women with polycystic ovary syndrome: a meta-analysis and systematic review. BMC Endocr. Disord. 2023; 23(1): 245. https://dx.doi.org/10.1186/s12902-023-01500-5
  3. Papaetis G.S., Kyriacou A. GLP-1 receptor agonists, polycystic ovary syndrome and reproductive dysfunction: current research and future horizons. Adv. Clin. Exp. Med. 2022; 31(11): 1265-74. https://dx.doi.org/10.17219/acem/151695
  4. Austregésilo de Athayde De Hollanda Morais B., Martins Prizão V., de Moura de Souza M., Ximenes Mendes B., Rodrigues Defante M.L., Cosendey Martins O. et al. The efficacy and safety of GLP-1 agonists in PCOS women living with obesity in promoting weight loss and hormonal regulation: a meta-analysis of randomized controlled trials. J. Diabetes Complications. 2024; 38(10): 108834. https://dx.doi.org/10.1016/j.jdiacomp.2024.108834
  5. Шабатукова Е.В., Щербань Д.А., Кудратова Е.А., Скворцова А.А., Жукова О.В. Современная фармакотерапия синдрома поликистозных яичников. Акушерство и гинекология. 2025; 7: 153-60. https://dx.doi.org/10.18565/aig.2025.83 [Shabatukova E.V., Shcherban D.A., Kudratova E.A., Skvortsova A.A., Zhukova O.V. Modern pharmacotherapy of polycystic ovary syndrome. Obstetrics and Gynecology. 2025; (7): 153-60 (in Russian). https://dx.doi.org/10.18565/aig.2025.83].
  6. Ye Z.R., Yan C.Q., Liao N., Wen S.H. The effectiveness and safety of exenatide versus metformin in patients with polycystic ovary syndrome: a meta-analysis of randomized controlled trials. Reprod. Sci. 2023; 30(8): 2349-61. https://dx.doi.org/10.1007/s43032-023-01222-y
  7. Salamun V., Jensterle M., Janez A., Vrtacnik-Bokal E. Liraglutide increases IVF pregnancy rates in obese PCOS women with poor response to first-line reproductive treatments: a pilot randomized study. Eur. J. Endocrinol. 2018; 179(1): 1-11. https://dx.doi.org/10.1530/EJE-18-0175
  8. Yang Q., Wang F. Successful pregnancy after improving insulin resistance with the glucagon-like peptide-1 analogue in a woman with polycystic ovary syndrome: a case report and review of the literature. Gynecol. Obstet. Invest. 2016; 81(5): 477-80. https://dx.doi.org/10.1159/000446951
  9. Барсуков И.А., Тазина Т.В., Фаниев М.В. Многогранность репродуктивных нарушений у пациентов с ожирением: взгляд эндокринолога, акушера-гинеколога и уролога. РМЖ. Мать и дитя. 2024; 7(3): 250-60. https://dx.doi.org/10.32364/2618-8430-2024-7-3-10 [Barsukov I.A., Tazina T.V., Faniev M.V. Versatility of reproductive disorders in obese patients: the view of endocrinologist, obstetrician-gynecologist and urologist. Russian Journal of Woman and Child Health. 2024; 7(3): 248-58 (in Russian). https://dx.doi.org/10.32364/2618-8430-2024-7-3-10].
  10. Kanda R., Hiraike H., Wada-Hiraike O., Ichinose T., Nagasaka K., Sasajima Y. et. al. Expression of the glucagon-like peptide-1 receptor and its role in regulating autophagy in endometrial cancer. BMC Cancer. 2018; 18(1): 657. https://dx.doi.org/10.1186/s12885-018-4570-8
  11. Hagemann A.R., Hagemann I.S., Mutch D.G., Devor E.J., Malmrose P.K., Zhang Y. et al. Enhancing progestin therapy with a glucagon-like peptide-1 agonist for the conservative management of endometrial cancer. Cancers (Basel). 2025; 17(4): 598. https://dx.doi.org/10.3390/cancers17040598
  12. Wang L., Xu R., Kaelber D.C., Berger N.A. Glucagon-Like peptide 1 receptor agonists and 13 obesity-associated cancers in patients with type 2 diabetes. JAMA Netw. Open. 2024; 7(7): e2421305. https://dx.doi.org/10.1001/jamanetworkopen.2024.21305
  13. Wang M., Dong T., Lucero M., Pan W., Wang X., Zhou L. et al. Association between glucagon-like peptide-1 receptor agonists and ovarian cancer survival: a population-based cohort study. Gynecol. Oncol. 2025; 199: 57-63. https://dx.doi.org/10.1016/j.ygyno.2025.06.012
  14. Jensterle M., Janez A., Fliers E., DeVries J.H., Vrtacnik-Bokal E., Siegelaar S.E. The role of glucagonlike peptide-1 in reproduction: from physiology to therapeutic perspective. Hum. Reprod. Update. 2019; 25(4): 504-17. https://dx.doi.org/10.1093/humupd/dmz019
  15. Athar F., Karmani M., Templeman N.M. Metabolic hormones are integral regulators of female reproductive health and function. Biosci. Rep. 2024; 44(1). https://dx.doi.org/10.1042/BSR20231916
  16. Khan D., Ojo O.O., Woodward O.R., Lewis J.E., Sridhar A., Gribble F.M. et. al. Evidence for involvement of GIP and GLP-1 receptors and the Gut-Gonadal axis in regulating female reproductive function in mice. Biomolecules. 2022; 12(12): 1736. https://dx.doi.org/10.3390/biom12121736
  17. Zhang Y., Lin Y., Li G., Yuan Y., Wang X., Li N. at. al. Glucagon-like peptide-1 receptor agonists decrease hyperinsulinemia and hyperandrogenemia in dehydroepiandrosterone-induced polycystic ovary syndrome mice and are associated with mitigating inflammation and inducing browning of white adipose tissue. Biol. Reprod. 2023; 108(6): 945-59. https://dx.doi.org/10.1093/biolre/ioad032
  18. Guo S., Li X., Liu M., Feng M., Wang X., Xue H. et. al. Semaglutide alleviates ovarian oxidative stress and autophagy via the PI3K/AKT/mTOR pathway in mice with polycystic ovary syndrome. Drug. Des. Devel. Ther. 2025; 19: 4297-310. https://dx.doi.org/10.2147/DDDT.S522730
  19. Горина К.А., Ходжаева З.С., Белоусов Д.М., Баранов И.И., Гохберг Я.А., Пащенко А.А. Преждевременные роды: прошлые ограничения и новые возможности. Акушерство и гинекология. 2020; 1: 12-9. https://dx.doi.org/10.18565/aig.2020.1.12-119 [Gorina K.A., Khodzhaeva Z.S., Belousov D.M., Baranov I.I., Gokhberg Ya.A., Pashchenko A.A. Premature birth: past restrictions and new opportunities. Obstetrics and Gynecology. 2020; (1): 12-9. (in Russian). https://dx.doi.org/10.18565/aig.2020.1.12-119].
  20. Liu M., Guo S., Li X., Tian Y., Yu Y., Tang L. et.al. Semaglutide alleviates ovary inflammation via the AMPK/SIRT1/NF-κB signaling pathway in polycystic ovary syndrome mice. Drug. Des. Devel. Ther. 2024; 18: 3925-38. https://dx.doi.org/10.2147/DDDT.S484531
  21. Sun Z., Li P., Wang X., Lai S., Qiu H., Chen Z. et. al. GLP-1/GLP-1R signaling regulates ovarian PCOS-associated granulosa cells proliferation and antiapoptosis by modification of forkhead box protein O1 phosphorylation sites. Int. J. Endocrinol. 2020; 2020: 1484321. https://dx.doi.org/10.1155/2020/1484321
  22. Artunc-Ulkumen B., Pala H.G., Pala E.E., Yavasoglu A., Yigitturk G., Erbas O. Exenatide improves ovarian and endometrial injury and preserves ovarian reserve in streptozocin induced diabetic rats. Gynecol. Endocrinol. 2014; 31(3):196-201. https://dx.doi.org/10.3109/09513590.2014.975686
  23. Wolszczak M., Wołodkiewicz H., Szmit J. The impact of GLP-1 receptor agonists on women’s reproductive health: a review. J. Educ., Health Sport. 2025; 82: 60194. https://dx.doi.org/10.12775/JEHS.2025.82.60194
  24. Pathare A., Apostolov A., Lavõgina D., Kask K., Risal S., Ruiz-Durán S. et. al. Impact of glucagon-like peptide-1 receptor (GLP-1R) agonist therapy on the endometrium and embryo: a boon to infertility? Hum. Reprod. 2025; 40. https://dx.doi.org/10.1093/humrep/deaf097.220
  25. Salamun V., Lovrecic L., Maver A., Peterlin B., Ban Frangez H., Riemma G. et al. Endometrial transcriptome changes following short-term liraglutide treatment in infertile women with polycystic ovarian syndrome and obesity. Gynecol. Obstet. Invest. 2026; 91(2): 241-50. https://dx.doi.org/10.1159/000547513
  26. Wu L., Zhan Y., Wang Y. Semaglutide may ameliorate fibrosis and inhibit epithelial–mesenchymal transition in intrauterine adhesion models. Int. J. Mol. Sci. 2024; 25(11): 6196. https://dx.doi.org/10.3390/ijms25116196
  27. Xiong C., Wu J., Ma Y., Li N., Wang X., Li Y. et. al. Effects of glucagon-like peptide-1 receptor agonists on gut microbiota in dehydroepiandrosterone-induced polycystic ovary syndrome mice: compared evaluation of liraglutide and semaglutide intervention. Diabetes Metab. Syndr. Obes. 2024; 17: 865-80. https://dx.doi.org/10.2147/DMSO.S451129
  28. Qiao L., Lu C., Zang T., Dzyuba B., Shao J. Maternal GLP-1 receptor activation inhibits fetal growth. Am. J. Physiol. Endocrinol. Metab. 2024; 326(3): E268-76. https://dx.doi.org/10.1152/ajpendo.00361.2023
  29. Dumolt J.H., Rosario F.J., Kramer A.C., Horwitz S., Powell T.L., Jansson T. Maternal glucagon-like peptide-1 is positively associated with fetal growth in pregnancies complicated with obesity. Clin. Sci. (Lond). 2023; 137(8): 663-78. https://dx.doi.org/10.1042/CS20220890
  30. Кан Н.Е., Солдатова Е.Е., Тютюнник В.Л., Борисова А.Г., Тезиков Ю.В., Липатов И.С., Садекова А.А., Алексеев А.А., Красный А.М. Факторы энергетического метаболизма при задержке роста плода. Акушерство и гинекология. 2024; 5: 44-52. https://dx.doi.org/10.18565/aig.2024.9 [Kan N.E., Soldatova E.E., Tyutyunnik V.L., Borisova A.G., Tezikov Y.V., Lipatov I.S., Sadekova A.A., Alekseev A.A., Krasnyi A.M. Factors of energy metabolism in fetal growth restriction. Obstetrics and Gynecology. 2024; (5): 44-52 (in Russian). https://dx.doi.org/10.18565/aig.2024.9].
  31. Красный А.М., Кан Н.Е., Борисова А.Г., Солдатова Е.Е., Тютюнник В.Л., Волочаева М.В. Влияние инкретина глюкагоноподобного пептида-1 на фенотипический профиль мононуклеарных клеток при задержке роста плода. Акушерство и гинекология. 2024; 10: 74-81. https://dx.doi.org/10.18565/aig.2024.156 [Krasnyi A.M., Kan N.E., Borisova A.G., Soldatova E.E., Tyutyunnik V.L., Volochaeva M.V.The effect of incretin hormone GLP-1 on the phenotypic profile of mononuclear cells in fetal growth restriction. Obstetrics and Gynecology. 2024; (10): 74-81 (in Russian). https://dx.doi.org/10.18565/aig.2024.156].
  32. Muller D.R.P., Stenvers D.J., Malekzadeh A., Holleman F., Painter R.C., Siegelaar S.E. Effects of GLP-1 agonists and SGLT2 inhibitors during pregnancy and lactation on offspring outcomes: a systematic review of the evidence. Front. Endocrinol. 2023; 14: 1215356. https://dx.doi.org/10.3389/fendo.2023.1215356
  33. Caruso I., Gioia L.D., Molfetta S.D., Cignarelli A., Palmer S.C., Natale P. et al. Glucometabolic outcomes of GLP-1 receptor agonist-based therapies in patients with type 2 diabetes: a systematic review and network meta-analysis. eClinicalMedicine. 2023; 64: 102181. https://dx.doi.org/10.1016/j.eclinm.2023.102181
  34. Wyckoff J.A., Lapolla A., Asias-Dinh B.D., Barbour L.A., Brown F.M., Catalano P.M. et. al. Preexisting diabetes and pregnancy: an Endocrine Society and European Society of Endocrinology Joint Clinical Practice Guideline. J. Clin. Endocrinol. Metabol. 2025; 110(9): 2405-52. https://dx.doi.org/10.1210/clinem/dgaf288
  35. Cesta C.E., Rotem R., Bateman B.T., Chodick G., Cohen J.M., Furu K. et al. Safety of GLP-1 receptor agonists and other secondline antidiabetics in early pregnancy. JAMA Intern. Med. 2024; 184(2): 144-52. https://dx.doi.org/10.1001/jamainternmed.2023.6663
  36. Armstrong B.B.S., Servidoni A.C.P., Martin G.C. de C., Machado G.F., Amador W.F.O., Yousif A. Evaluation of GLP-1 receptor agonists in obstetrics and perinatal outcomes: a systematic review and meta-analysis. J. Gynecol. Obstet. Hum. Reprod. 2025; 54(10): 103046. https://dx.doi.org/10.1016/j.jogoh.2025.103046
  37. Parker C.H., Slattery C., Brennan D.J., le Roux C.W. Glucagon-like peptide 1 receptor agonists' use during pregnancy: Safety data from regulatory clinical trials. Diabetes Obes. Metab. 2025; 27(8): 4102-08. https://dx.doi.org/10.1111/dom.16437
  38. Drummond R.F., Seif K.E., Reece E.A. Glucagon-like peptide-1 receptor agonist use in pregnancy: a review. Am. J. Obstet. Gynecol. 2025; 232(1): 17-25. https://dx.doi.org/10.1016/j.ajog.2024.08.024
  39. Kolding L., Henriksen J.N., Sædder E.A., Ovesen P.G., Pedersen L.H. Pregnancy outcomes after semaglutide exposure. Basic Clin. Pharmacol. Toxicol. 2025; 136(4): e70021. https://dx.doi.org/10.1111/bcpt.70021
  40. Imbroane M.R., LeMoine F., Nau C.T. Preconception glucagon-like peptide-1 receptor agonist use associated with decreased risk of adverse obstetrical outcomes. Am. J. Obstet. Gynecol. 2025; 233(2): 116.e1-e7. https://dx.doi.org/10.1016/j.ajog.2025.01.019
  41. Skov K., Mandic I.N., Nyborg K.M. Semaglutide and pregnancy. Int. J. Gynecol. Obstet. 2023; 163(2): 700-1. https://dx.doi.org/10.1002/ijgo.15092
  42. Livadas S., Macut D., Bothou C., Kuliczkowska-Płaksej J., Vryonidou A., Bjekic-Macut J. et al. Insulin resistance, androgens, and lipids are gradually improved in an age-dependent manner in lean women with polycystic ovary syndrome: insights from a large Caucasian cohort. Hormones. 2020; 19(4): 531-39. https://dx.doi.org/10.1007/s42000-020-00211-z
  43. Alghamdi A., Alsaeddi A., Malki H., Alsaedi A. A case report of a pregnant woman with type 2 diabetes mellitus using dulaglutide during the first trimester of pregnancy. Cureus. 2023; 15(9): e44644. https://dx.doi.org/10.7759/cureus.44644
  44. Burlina S., Cioccoloni D., Romanello G., Lombardi S. Dulaglutide plus dapaglifozin use until the second trimester of pregnancy in a woman with type 2 diabetes. Acta Diabetol. 2025; 63: 343-5. https://dx.doi.org/10.1007/s00592-025-02601-4
  45. Molteni M., Lodigiani S., Teliti M., Rotondi M., Guazzoni V. Use of dulaglutide in a pregnant woman with type 2 diabetes until third trimester of pregnancy. Acta Diabetol. 2024; 61(11): 1491-4. https://dx.doi.org/10.1007/s00592-024-02331-z
  46. Greco D. Normal pregnancy outcome after first-trimester exposure to liraglutide in a woman with type 2 diabetes. Diabetic Med. 2015; 32(10): e29–30. https://dx.doi.org/10.1111/dme.12726
  47. Ivanišević M., Herman M., Horvatiček M., Lovrenčić Vučić M., Đelmiš J. Pregnancy outcome and liraglutide levels in serum and umbilical vein blood of a woman with type 2 diabetes. A case report. Gynaecol. Perinatol. 2018; 27(3-4): 70-2.
  48. Williams J., Pomeroy N.E., Pop-Busui R., Lash R., Douyon L., Chames M. et al. Case report: exenatide use during pregnancy. Endocrinol. 2009; 19(3): 119-21. https://dx.doi.org/10.1097/TEN.0b013e3181a5875e
  49. Doğan G.O., Erbaş O. Exenatide improves cisplatin induced ovarian damage through NLRP3, Nrf-2, and TLR4 pathways. Cir. Cir. 2024; 93(1): 35-40. https://dx.doi.org/10.24875/CIRU.23000304
  50. Мелкозерова О.А., Мурзин А.В., Третьякова Т.Б., Дерябина Е.Г. Молекулярно-генетические предикторы перинатальных осложнений гестационного сахарного диабета у беременных после применения вспомогательных репродуктивных технологий. РМЖ. Мать и дитя. 2024; 7(1): 4-11 https://dx.doi.org/10.32364/2618-8430-2024-7-1-1 [Melkozerova O.A., Murzin A.V., Tretyakova T.B., Deryabina E.G. Molecular and genetic predictors of perinatal complications of gestational diabetes mellitus in pregnant women after the use of assisted reproductive technologies. RMJ. Mother and child. 2024; 7(1): 4-11. (in Russian). https://dx.doi.org/10.32364/2618-8430-2024-7-1-1].
  51. Diab H., Fuquay T., Datta P., Bickel U., Thompson J., Krutsch K. Subcutaneous semaglutide during breastfeeding: infant safety regarding drug transfer into human milk. Nutrients. 2024; 16(17): 2886. https://dx.doi.org/10.3390/nu16172886
  52. Min T., Bain S.C. The role of tirzepatide, dual GIP and GLP-1 receptor agonist, in the management of type 2 diabetes: the SURPASS clinical trials. Diabetes Ther. 2021; 12(1): 143-57. https://dx.doi.org/10.1007/s13300-020-00981-0
  53. Gallwitz B. Clinical perspectives on the use of the GIP/GLP-1 receptor agonist tirzepatide for the treatment of type-2 diabetes and obesity. Front. Endocrinol. 2022; 13: 1004044. https://dx.doi.org/10.3389/fendo.2022.1004044
  54. Мкртумян А.М., Егшатян Л.В. Отечественный твинкретин Седжаро: один препарат – несколько мишеней. Эффективная фармакотерапия. 2025; 21(46): 30-6. https://dx.doi.org/10.33978/2307-3586-2025-21-46-30-36 [Mkrtumyan A.M., Egshatyan L.V. Russian-made twincretin Sejaro: one medicine – multiple targets. Effective pharmacotherapy. 2025; 21(46): 30-6 (in Russian). https://dx.doi.org/10.33978/2307-3586-2025-21-46-30-36].
  55. Coskun T., Urva S., Roell W.C., Qu H., Loghin C., Moyers J.S. et. al. LY3437943, a novel triple glucagon, GIP, and GLP-1 receptor agonist for glycemic control and weight loss: from discovery to clinical proof of concept. Cell Metabolism. 2022; 34(9): 1234-47.e9. https://dx.doi.org/10.1016/j.cmet.2022.07.013
  56. Jastreboff A.M., Kaplan L.M., Frías J.P., Wu Q., Du Y., Gurbuz S. et. al. Triple–hormone-receptor agonist retatrutide for obesity – a phase 2 trial. N. Engl. J. Med. 2023; 389(6): 514-26. https://dx.doi.org/10.1056/NEJMoa2301972
  57. Bomholt A.B., Johansen C.D., Christensen J.B., Kjeldsen S.A.S., Galsgaard K.D., Winther-Sørensen M. et. al. Evaluation of commercially available glucagon receptor antibodies and glucagon receptor expression. Commun. Biol. 2022; 5(1): 1278. https://dx.doi.org/10.1038/s42003-022-04242-7
  58. Cilvik S.N., Wesolowski S.R., Anthony R.V., Brown L.D., Rozance P.J. Late gestation fetal hyperglucagonaemia impairs placental function and results in diminished fetal protein accretion and decreased fetal growth. J. Physiol. 2021; 599(13): 3403-27. https://dx.doi.org/10.1113/JP281288
  59. Şentürk Ş., Hatirnaz S., Kanat-Pektaş M. Serum preptin and amylin levels with respect to body mass index in polycystic ovary syndrome patients. Med. Sci. Monit. 2018; 24: 7517-23. https://dx.doi.org/10.12659/MSM.912957

Received 15.12.2025

Accepted 05.06.2026

About the Authors

Svetlana V. Dora, Dr. Med. Sci., Professor, Department of Faculty Therapy, Pavlov First Saint Petersburg State Medical University, Ministry of Health of the Russian Federation, 197022, Russia, St. Petersburg, L’va Tolstogo str., 6-8, doras2001@mail.ru, https://orcid.org/0000-0002-8249-6075
Yuri Sh. Khalimov, Dr. Med. Sci., Professor, Head of the Department of Faculty Therapy, Pavlov First Saint Petersburg State Medical University, Ministry of Health of Russia, 197022, Russia, St. Petersburg, L’va Tolstogo str., 6-8, yushkha@gmail.com, https://orcid.org/0000-0002-7755-7275
Vitaly F. Bezhenar, Dr. Med. Sci., Professor, Head of the Department of Obstetrics, Gynecology and Reproductology, Pavlov First Saint Petersburg State Medical University, Ministry of Health of Russia, 197022, Russia, St. Petersburg, L’va Tolstogo str., 6-8, bez-vitaly@yandex.ru, https://orcid.org/0000-0002-7558-7657
Anna V. Lisker, PhD, Head of Endocrinology Department, Clinical Endocrinology Center, Pavlov First Saint Petersburg State Medical University, Ministry of Health of Russia, 197022, Russia, St. Petersburg, L’va Tolstogo str., 6-8, a.lisker@mail.ru, https://orcid.org/0000-0003-4295-1202
Zlata V. Shvets, PhD student in Endocrinology, Department of Faculty Therapy, Pavlov First Saint Petersburg State Medical University, Ministry of Health of Russia, 197022, Russia, St. Petersburg, L’va Tolstogo str., 6-8, +7(911)848-73-75, shvetszlata31@gmail.com, https://orcid.org/0009-0007-9218-8133
Anna R. Volkova, Dr. Med. Sci., Professor, Department of Faculty Therapy, Pavlov First Saint Petersburg State Medical University, Ministry of Health of Russia, 197022, Russia, St. Petersburg, L’va Tolstogo str., 6-8, volkovaa@mail.ru, https://orcid.org/0000-0002-5189-9365
Alexandra B. Kolyabina, Resident in Endocrinology, Department of Faculty Therapy, Pavlov First Saint Petersburg State Medical University, Ministry of Health of Russia, 197022, Russia, St. Petersburg, L’va Tolstogo str., 6-8, kolyabinas@yandex.ru, https://orcid.org/0009-0003-3136-3509
Olga S. Murzina, Student, Pavlov First Saint Petersburg State Medical University, Ministry of Health of Russia, 197022, Russia, St. Petersburg, L’va Tolstogo str., 6-8, olyamurzinaa@yandex.ru, https://orcid.org/0009-0005-4712-7871
Corresponding author: Zlata V. Shvets, shvetszlata31@gmail.com

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