1. Андреева Е.Н., Шереметьева Е.В., Фурсенко В.А. Ожирение — угроза репродуктивного потенциала России. Ожирение и метаболизм. 2019;16(3):20–28. DOI: 10.14341/omet10340. Andreeva E.N., Sheremetyeva E.V., Fursenko V.A. Obesity — threat to the reproductive potential of Russia. Obesity and metabolism. 2019;16(3):20–28 (in Russ.). DOI: 10.14341/omet10340
2. Алфеерова В.И., Мустафина С.В. Распространенность ожирения во взрослой популяции Российской Федерации (обзор литературы). Ожирение и метаболизм. 2022;19(1):96–105. DOI: 10.14341/omet12809. Alferova V.I., Mustafina S.V. The prevalence of obesity in the adult population of the Russian Federation (literature review). Obesity and metabolism. 2022;19(1):96–105 (in Russ.). DOI: 10.14341/omet12809
3. Souter I., Baltagi L.M., Kuleta D. et al. Women, weight, and fertility: the effect of body mass index on the outcome of superovulation/intrauterine insemination cycles. Fertil Steril. 2011;95(3):1042–1047. DOI: 10.1016/j.fertnstert.2010.11.062
4. Sermondade N., Huberlant S., Bourhis-Lefebvre V. et al. Female obesity is negatively associated with live birth rate following IVF: a systematic review and meta-analysis. Hum Reprod Update. 2019;25(4):439–451. DOI: 10.1093/humupd/dmz011
5. Teede H.J., Khomami M.B., Morman R. et al. Polyendocrine metabolic ovarian syndrome, the new name for polycystic ovary syndrome: a multistep global consensus process. Lancet. 2026;407(10545):2329–2339. DOI: 10.1016/S0140-6736(26)00717-8
6. Wei S., Schmidt M.D., Dwyer T. et al. Obesity and menstrual irregularity: associations with SHBG, testosterone, and insulin. Obesity (Silver Spring). 2009;17(5):1070–1076. DOI: 10.1038/oby.2008.641
7. Itoi S., Sampei M., Tatsumi T. et al. Body mass index and menstrual irregularity in a prospective cohort study of smartphone application users. npj Women's Health. 2025;3(1):16. DOI: 10.1038/s44294-025-00065-z
8. Gesink Law D.C., Maclehose R.F., Longnecker M.P. Obesity and time to pregnancy. Hum Reprod. 2007;22(2):414–420. DOI: 10.1093/humrep/del400
9. Van der Steeg J.W., Steures P., Eijkemans M.J.C. et al. Obesity affects spontaneous pregnancy chances in subfertile, ovulatory women. Hum Reprod. 2008;23(2):324–328. DOI: 10.1093/humrep/dem371
10. Boxem A.J., Blaauwendraad S.M., Mulders A.G.M.G.J. et al. Preconception and Early-Pregnancy Body Mass Index in Women and Men, Time to Pregnancy, and Risk of Miscarriage. JAMA Netw Open. 2024;7(9):e2436157. DOI: 10.1001/jamanetworkopen.2024.36157
11. Diamanti-Kandarakis E., Dunaif A. Insulin resistance and the polycystic ovary syndrome revisited: an update on mechanisms and implications for pathogenesis. Endocr Rev. 2012;33(6):981–1030. DOI: 10.1210/er.2011-1034
12. Patel A.H., Koysombat K., Pierret A. et al. Kisspeptin in functional hypothalamic amenorrhea: Pathophysiology and therapeutic potential. Ann N Y Acad Sci. 2024;1540(1):21–46. DOI: 10.1111/nyas.15220
13. Chen Y., Wang R., Zhang N., Xu L. The dual burden of obesity: decoding metabolism and female reproductive endocrinology. Front Physiol. 2025;16:1627607. DOI: 10.3389/fphys.2025.1627607
14. Broughton D.E., Moley K.H. Obesity and female infertility: potential mediators of obesity's impact. Fertil Steril. 2017;107(4):840–847. DOI: 10.1016/j.fertnstert.2017.01.017
15. Stothard B.J., Tennant P.W.G., Bell R. et al. Maternal overweight and obesity and the risk of congenital anomalies: a systematic review and meta-analysis. JAMA. 2009;301(6):636–650. DOI: 10.1001/jama.2009.113
16. Chu S.Y., Callaghan W.M., Kim S.Y. et al. Maternal obesity and risk of gestational diabetes mellitus. Diabetes Care. 2007;30(8):2070–2076. DOI: 10.2337/dc06-2559a
17. O'Brien T.E., Ray J.G., Chan W.S. Maternal body mass index and the risk of preeclampsia: a systematic overview. Epidemiology. 2003;14(3):368–374. DOI: 10.1097/00001648-200305000-00020
18. Chu S.Y., Kim S.Y., Schmid C.H. et al. Maternal obesity and risk of cesarean delivery: a meta-analysis. Obes Rev. 2007;8(5):385–394. DOI: 10.1111/j.1467-789X.2007.00397.x
19. Zhang C., Wu Y., Li S., Zhang D. Maternal prepregnancy obesity and the risk of shoulder dystocia: a meta-analysis. BJOG. 2018;125(4):407–413. DOI: 10.1111/1471-0528.14841
20. Zhang J., Bricker L., Wray S., Quenby S. Poor uterine contractility in obese women. BJOG. 2007;114(3):343–348. DOI: 10.1111/j.1471-0528.2006.01233.x
21. Heslehurst N., Simpson H., Ells L.J. et al. The impact of maternal BMI status on pregnancy outcomes with immediate short-term obstetric resource implications: a meta-analysis. Obes Rev. 2008;9(6):635–683. DOI: 10.1111/j.1467-789X.2008.00511.x
22. Rasmussen K.M., Kjolhede C.L. Prepregnant overweight and obesity diminish the prolactin response to suckling in the first week postpartum. Pediatrics. 2004;113(5):e465–e471. DOI: 10.1542/peds.113.5.e465
23. Sharp G.C., Salas L.A., Monnereau C. et al. Maternal BMI at the start of pregnancy and offspring epigenome-wide DNA methylation: findings from the pregnancy and childhood epigenetics (PACE) consortium. Hum Mol Genet. 2017;26(20):4067–4085. DOI: 10.1093/hmg/ddx290
24. Aune D., Saugstad O.D., Henriksen T., Tonstad S. Maternal body mass index and the risk of fetal death, stillbirth, and infant death: a systematic review and meta-analysis. JAMA. 2014;311(15):1536–1546. DOI: 10.1001/jama.2014.2269
25. American Diabetes Association. 15. Management of Diabetes in Pregnancy: Standards of Care in Diabetes — 2025. Diabetes Care. 2025;48(Suppl 1):S306–S320. DOI: 10.2337/dc25-S015
26. Sustarsic A., Hadzic V., Meulenberg C.J.W. et al. The influence of lifestyle interventions and overweight on infertility: a systematic review, meta-analysis, and meta-regression of randomized controlled trials. Front Med (Lausanne). 2023;10:1264947. DOI: 10.3389/fmed.2023
27. Legro R.S., Hansen K.R., Diamond M.P. et al. Effects of preconception lifestyle intervention in infertile women with obesity: the FIT-PLESE randomized controlled trial. PLoS Med. 2022;19(1):e1003883. DOI: 10.1371/journal.pmed.1003883
28. Wang Z., Van Faassen M., Groen H. et al. Resumption of ovulation in anovulatory women with PCOS and obesity is associated with reduction of 11β-hydroxyandrostenedione concentrations. Hum Reprod. 2024;39(5):1078–1088. DOI: 10.1093/humrep/deae058
29. Coskun T., Sloop K.W., Loghin C. et al. LY3298176, a novel dual GIP and GLP-1 receptor agonist for the treatment of type 2 diabetes mellitus: from discovery to clinical proof of concept. Mol Metab. 2018;18:3–14. DOI: 10.1016/j.molmet.2018.09.009
30. Look M., Dunn J.P., Kushner R.F. et al. Body composition changes during weight reduction with tirzepatide in the SURMOUNT-1 study of adults with obesity or overweight. Diabetes Obes Metab. 2025;27(5):2720–2729. DOI: 10.1111/dom.16275
31. Tchang B.G., Mihai A.C., Stefanski A. et al. Body weight reduction in women treated with tirzepatide by reproductive stage: a post hoc analysis from the SURMOUNT program. Obesity (Silver Spring). 2025;33(5):851–860. DOI: 10.1002/oby.24254
32. Aronne L.J., Horn D.B., le Roux C.W. et al. Tirzepatide as compared with semaglutide for the treatment of obesity. N Engl J Med. 2025;393(1):26–36. DOI: 10.1056/NEJMoa2416394
33. Pi-Sunyer X., Astrup A., Fujioka K. et al. A randomized, controlled trial of 3.0 mg of liraglutide in weight management. N Engl J Med. 2015;373(1):11–22. DOI: 10.1056/NEJMoa1411892
34. Wilding J.P.H., Batterham R.L., Calanna S. et al. Once-weekly semaglutide in adults with overweight or obesity. N Engl J Med. 2021;384(11):989–1002. DOI: 10.1056/NEJMoa2032183
35. Kolli R.T., Aoutla S., Jyothi N. et al. Rebound or Retention: A Meta-Analysis of Weight Regain After the Discontinuation of Glucagon-Like Peptide-1 (GLP-1) Receptor Agonists and Other Anti-obesity Drugs. Cureus. 2025;17(10):e94926. DOI: 10.7759/cureus.94926
36. Aronne L.J., Sattar N., Horn D.B. et al. Continued treatment with tirzepatide for maintenance of weight reduction in adults with obesity: the SURMOUNT-4 randomized clinical trial. JAMA. 2024;331(1):38–48. DOI: 10.1001/jama.2023.24945
37. Broughton D.E., Jungheim E.S. A focused look at obesity and the preimplantation trophoblast. Semin Reprod Med. 2016;34(1):5–10. DOI: 10.1055/s-0035-1570032
38. De-Regil L.M., Palacios C., Lombardo L.K. et al. Vitamin D supplementation for women during pregnancy. Cochrane Database Syst Rev. 2016;(1):CD008873. DOI: 10.1002/14651858.CD008873.pub3
39. Hviid K.V.R., Banasik K., Mortensen L.H. et al. Periconceptional GLP-1 receptor agonist exposure and obstetric outcomes: a Danish nationwide cohort study. Hum Reprod Open. 2026;2026(2):hoag015. DOI: 10.1093/hropen/hoag015
40. Dao K., Shechtman S., Weber-Schoendorfer C. et al. Use of GLP1 receptor agonists in early pregnancy and reproductive safety: a multicentre, observational, prospective cohort study based on the databases of six Teratology Information Services. BMJ Open. 2024;14(4):e083550. DOI: 10.1136/bmjopen-2023-083550
41. Cesta C.E., Rotem R., Bateman B.T. et al. Safety of GLP-1 Receptor Agonists and Other Second-Line Antidiabetics in Early Pregnancy. JAMA Intern Med. 2024;184(2):144–152. DOI: 10.1001/jamainternmed.2023.6663
42. Liu X., Xiong B., Yang R. et al. Periconceptional use of GLP-1 receptor agonists and the risk of major congenital malformations: a systematic review and meta-analysis. Endocr Connect. 2026;15(7):e260280. DOI: 10.1530/EC-26-0280
43. Brown J.P., Huybrechts K.F., Straub L. et al. Continuing Glucagon-Like Peptide-1 Receptor Agonists Into the First Trimester of Pregnancy and Pregnancy Outcomes: A Target Trial Emulation Study Using Claims Information. Ann Intern Med. 2026;179(7):929–937. DOI: 10.7326/ANNALS-25-04820
44. Uysal N., Horoz E., Gungor M. et al. Pregnancy outcomes following maternal GLP-1 receptor agonist exposure: a systematic review and meta-analysis. Sci Rep. 2026. DOI: 10.1038/s41598-026-61582-8
45. Kodali L.S.M., Metlock F.E., Nriagu B.N. et al. GLP-1 receptor agonist exposure during pregnancy: a systematic review and meta-analysis of adverse pregnancy outcomes. JACC Adv. 2026;5(6):102649. DOI: 10.1016/j.jacadv.2026.102649
46. Ozbek L., Shah E., Al-Shiab R. et al. Safety of GLP-1 and dual GLP-1/GIP receptor agonists in preconception, pregnancy, and lactation: a systematic review of maternal, fetal, and neonatal outcomes. Diabetes Obes Metab. 2026;28(6):4503–4528. DOI: 10.1111/dom.70699
47. Banerjee M., Dutta S., Dasgupta S. Pre-pregnancy GLP-1 receptor agonist or tirzepatide use and gestational diabetes risk: evaluating pharmacodynamic carry-over versus post-discontinuation metabolic rebound in a multinational federated cohort. Diabetes Obes Metab. 2026;28(7):6370–6379. DOI: 10.1111/dom.70853
48. Goldstein R.F., Bahri Khomami M., Tay C.T. et al. Gestational weight gain and risk of adverse maternal and neonatal outcomes in observational data from 1.6 million women: systematic review and meta-analysis. BMJ. 2025;391:e085710. DOI: 10.1136/bmj-2025-085710
49. Ye X., Li P., Shi C. Association between gestational weight gain and adverse pregnancy outcomes: a systematic review and meta-analysis. Front Glob Womens Health. 2026;7:1777069. DOI: 10.3389/fgwh.2026.1777069
50. Yang D., Yu Z., Chen J. et al. Association Between First-Trimester Gestational Weight Gain and the Risks of Gestational Diabetes Mellitus and Macrosomia. Diabetes Metab Syndr Obes. 2026;19:564746. DOI: 10.2147/DMSO.S564746
51. Луговик И.А., Бабина А.В., Арутюнян С.С. и др. Первый дженерик тирзепатида GP30931: физико-химическое и биологическое сходство с референтным лекарственным средством. Разработка и регистрация лекарственных средств. 2025;14(2):54–74. DOI: 10.33380/2305-2066-2025-14-2-2084. Lugovik I.A., Babina A.V., Arutyunyan S.S. et al. The first generic tirzepatide GP30931: physicochemical and biological similarity to the reference drug. Drug development & registration. 2025;14(2):54–74 (in Russ.) DOI: 10.33380/2305-2066-2025-14-2-2084