Stress and microbiocenosis of the female reproductive tract
https://doi.org/10.17749/2313-7347/ob.gyn.rep.2026.808
Abstract
Aim: to systematically evaluate the evidence on psychosocial stress impacting on the microbiocenosis of the female reproductive tract and to delineate the underlying pathogenetic mechanisms.
Materials and Methods. A comprehensive literature review was conducted across PubMed/MEDLINE, Google Academy, and eLibrary databases covering a 25-year period. Search terms for query included "stress," "vaginal microbiome/microbiocenosis/microflora," "cervical microbiome," and "uterine microbiome" in both Russian and English. Original studies, systematic reviews, and meta-analyses were included; animal experiments, conference abstracts, non-full-text publications, and off-topic articles were excluded.
Results. Chronic psychosocial stress activates the hypothalamic-pituitary-adrenal axis and the sympathoadrenal system, leading to hypercortisolemia and elevated catecholamine levels. Key pathogenetic mechanisms include Th1-to-Th2 (T-helpers 1/T-helpers 2) immune shift followed by consequently suppressed cell-mediated immunity, estrogen deficiency-driven reduction of vaginal epithelial glycogen, impaired glucose metabolism, and direct catecholamine-mediated enhancement of bacterial virulence and proliferation. In the lower reproductive tract, stress is an independent predictor of bacterial vaginosis, recurrent vulvovaginal candidiasis, genital herpes reactivation, and high-risk human papillomavirus (HPV) persistence with increased risk of cervical intraepithelial neoplasia and invasive cervical cancer. Stress also elevates susceptibility to sexually transmitted infections. In the upper reproductive tract, depression and anxiety are associated with increased incidence of pelvic inflammatory disease and reduced implantation success in assisted reproductive technology programs.
Conclusion. Psychosocial stress is an independent, modifiable risk factor for reproductive tract dysbiosis. Assessing psychosocial status should be integrated into clinical evaluation of women with inflammatory and dysbiotic conditions of the reproductive tract, and psychological intervention should be considered a component of comprehensive treatment strategies.
About the Authors
A. V. TutovaRussian Federation
Anna V. Tutova, MD.
8/9 Nekrasova Str., Belgorod 308000
O. P. Lebedeva
Russian Federation
Olga P. Lebedeva, MD, Dr Sci Med, Prof.
Scopus Author ID: 55655876400.
WoS ResearcherID: E-5969-2015.
eLibrary SPIN-code: 9201-0850.
6 Miklukho-Maklaya Str., Moscow 117198;
85 Pobedy Str., Belgorod 308015
E. P. Kaluzhnova
Russian Federation
Elena P. Kaluzhnova
85 Pobedy Str., Belgorod 308015
M. K. Chadyuk
Russian Federation
Maria K. Chadyuk
85 Pobedy Str., Belgorod 308015
O. N. Kozarenko
Russian Federation
Olesya N. Kozarenko, MD, PhD.
Scopus Author ID: 57443919600.
eLibrary SPIN-code: 8670-3005.
85 Pobedy Str., Belgorod 308015
I. V. Kalashnikova
Russian Federation
Irina V. Kalashnikova, MD, PhD.
8/9 Nekrasova Str., Belgorod 308000;
85 Pobedy Str., Belgorod 308015
A. V. Nagorny
Russian Federation
Andrey V. Nagorny, MD, PhD.
8/9 Nekrasova Str., Belgorod 308000;
85 Pobedy Str., Belgorod 308015
A. V. Selivanova
Russian Federation
Alina V. Selivanova, MD, PhD.
85 Pobedy Str., Belgorod 308015;
46 Gubkina Str., Belgorod 308036
References
1. McEwen B.S. Stress, adaptation, and disease. Allostasis and allostatic load. Ann N Y Acad Sci. 1998;840:33–44. https://doi.org/10.1111/j.1749-6632.1998.tb09546.x.
2. Smith M.D., Wesselbaum D. Global evidence on the prevalence of and risk factors associated with stress. J Affect Disord. 2025;374:179–83. https://doi.org/10.1016/j.jad.2025.01.053.
3. Altemus M., Sarvaiya N., Neill Epperson C. Sex differences in anxiety and depression clinical perspectives. Front Neuroendocrinol. 2014;35(3):320–30. https://doi.org/10.1016/j.yfrne.2014.05.004.
4. Mahmud S., Mohsin M., Dewan M.N. et al. global prevalence of depression, anxiety, stress, and insomnia among general population during COVID-19 pandemic: A systematic review and meta-analysis. Trends in Psychol. 2023;31(1):143–70. https://doi.org/10.1007/s43076-021-00116-9.
5. Ebzeeva E.Yu., Polyakova O.A. Stress and stress-induced disorders. Meditsinskiy sovet. 2022;16(2):127–33. (In Russ.). https://doi.org/10.21518/2079-701X-2022-16-2-127-133.
6. Gomanova L.I., Balanova Yu.A., Evstifeeva S.E. et al. Psychoemotional stress as a risk factor for the development of noncommunicable diseases. Profilakticheskaya meditsina. 2023;26(8):114–20. (In Russ.). https://doi.org/10.17116/profmed202326081114.
7. Kim K., Tsai A.C., Sumner J.A., Jung S.J. Posttraumatic stress disorder, cardiovascular disease outcomes and the modifying role of socioeconomic status. J Affect Disord. 2022;319:555–61. https://doi.org/10.1016/j.jad.2022.09.117.
8. Biltz R.G., Sawicki C.M., Sheridan J.F. et al. The neuroimmunology of social-stress-induced sensitization. Nat Immunol. 2022;23(11):1527–35. https://doi.org/10.1038/s41590-022-01321-z.
9. Smirnova Y.D., Gryaznova M.V., Burakova I.Y. et al. Study of microbiome aberrations in patients with irritable bowel syndrome with diarrhea by next-generation sequencing. Research Results in Biomedicine. 2023;9(4):446–60. (In English). https://doi.org/10.18413/2658-6533-2023-9-4-0-2.
10. Valdes A.M., Walter J., Segal E., Spector T.D. Role of the gut microbiota in nutrition and health. BMJ. 2018;361:k2179. https://doi.org/10.1136/bmj.k2179.
11. Ogunrinola G.A., Oyewale J.O., Oshamika O.O., Olasehinde G.I. The human microbiome and its impacts on health. Int J Microbiol. 2020;2020(1):8045646. https://doi.org/10.1155/2020/8045646.
12. Foster J.A., Rinaman L., Cryan J.F. Stress & the gut-brain axis: regulation by the microbiome. Neurobiol Stress. 2017;7:124–36. https://doi.org/10.1016/j.ynstr.2017.03.001.
13. Marwaha K., Cain R., Asmis K. et al. Exploring the complex relationship between psychosocial stress and the gut microbiome: implications for inflammation and immune modulation. J Appl Physiol. 2025;138(2):518–35. https://doi.org/10.1152/japplphysiol.00652.2024.
14. Delgadillo D.R., Borelli J.L., Mayer E.A. et al. Biological, environmental, and psychological stress and the human gut microbiome in healthy adults. Sci Rep. 2025;15(1):362. https://doi.org/10.1038/s41598-024-77473-9.
15. Ma L., Yan Y., Webb R.J. et al. Psychological stress and gut microbiota composition: a systematic review of human studies. Neuropsychobiology. 2023;82(5):247–62. https://doi.org/10.1159/000533131.
16. Stoy S., McMillan A., Ericsson A.C., Brooks A.E. The effect of physical and psychological stress on the oral microbiome. Front Psychol. 2023;14:1166168. https://doi.org/10.3389/fpsyg.2023.1166168.
17. Amabebe E., Anumba D.O.C. Psychosocial stress, cortisol levels, and maintenance of vaginal health. Front Endocrinol. 2018;9:568. https://doi.org/10.3389/fendo.2018.00568.
18. Swidsinski S., Moll W.M., Swidsinski A. Bacterial vaginosis – vaginal polymicrobial biofilms and dysbiosis. Dtsch Arztebl Int. 2023;120(20): 347–54. https://doi.org/10.3238/arztebl.m2023.0090.
19. Jones C., Gwenin C. Cortisol level dysregulation and its prevalence – Is it nature's alarm clock? Physiol Rep. 2021;8(24):e14644. https://doi.org/10.14814/phy2.14644.
20. Rozanov V.A. Stress and mental health (neurobiological aspects). Social'naya i klinicheskaya psihiatriya. 2013;23(1):79–86. (In Russ.).
21. Strehl C., Ehlers L., Gaber T., Buttgereit F. Glucocorticoids – all-rounders tackling the versatile players of the immune system. Front Immunol. 2019;10:1744. https://doi.org/10.3389/fimmu.2019.01744.
22. Kuo T., McQueen A., Chen T.C., Wang J.C. Regulation of glucose homeostasis by glucocorticoids. In: Glucocorticoid signaling: from molecules to mice to man. NY: Springer, 2015. 99–126. https://doi.org/10.1007/978-1-4939-2895-8_5.
23. Valsamakis G., Papatheodorou D.C., Chalarakis N. M, et al. In pregnancy increased maternal STAI trait stress score shows decreased insulin sensitivity and increased stress hormones. Psychoneuroendocrinology. 2017;84:11–6. https://doi.org/10.1016/j.psyneuen.2017.06.008.
24. Lee M.J., Pramyothin P., Karastergiou K., Fried S.K. Deconstructing the roles of glucocorticoids in adipose tissue biology and the development of central obesity. Biochim Biophys Acta. 2014;1842(3):473–81. https://doi.org/10.1016/j.bbadis.2013.05.029.
25. Mazgelytė E., Karčiauskaitė D. Cortisol in metabolic syndrome. Adv Clin Chem. 2024;123:129–56. https://doi.org/10.1016/bs.acc.2024.06.008.
26. Cain D.W., Cidlowski J.A. Immune regulation by glucocorticoids. Nat Rev Immunol. 2017;17(4):233–47. https://doi.org/10.1038/nri.2017.1.
27. Busillo J.M., Cidlowski J.A. The five Rs of glucocorticoid action during inflammation: ready, reinforce, repress, resolve, and restore. Trends Endocrinol Metab. 2013;24(3):109–19. https://doi.org/10.1016/j.tem.2012.11.005.
28. De Bosscher K., Vanden Berghe W., Haegeman G. The interplay between the glucocorticoid receptor and nuclear factor-kappaB or activator protein-1: molecular mechanisms for gene repression. Endocr Rev. 2003;24(4):488–522. https://doi.org/10.1210/er.2002-0006.
29. Padgett D.A., Glaser R. How stress influences the immune response. Trends Immunol. 2003;24(8):444–8. https://doi.org/10.1016/s1471-4906(03)00173-x.
30. Elenkov I.J., Chrousos G.P. Stress hormones, proinflammatory and antiinflammatory cytokines, and autoimmunity. Ann N Y Acad Sci. 2002;966:290–303. https://doi.org/10.1111/j.1749-6632.2002.tb04229.x.
31. Naglak E.K., Morrison S.G., Morrison R.P. Gamma interferon is required for optimal antibody-mediated immunity against genital Chlamydia infection. Infect Immun. 2016;84(11):3232–42. https://doi.org/10.1128/IAI.00749-16.
32. Tang V.A., Rosenthal K.L. Intravaginal infection with herpes simplex virus type-2 (HSV-2) generates a functional effector memory T cell population that persists in the murine genital tract. J Reprod Immunol. 2010;87(1–2):39–44. https://doi.org/10.1016/j.jri.2010.06.155.
33. Alotiby A. Immunology of stress: a review article. J Clin Med. 2024;13(21):6394. https://doi.org/10.3390/jcm13216394.
34. Lei Y., Liao F., Tian Y. et al. Investigating the crosstalk between chronic stress and immune cells: implications for enhanced cancer therapy. Front Neurosci. 2023;17:1321176. https://doi.org/10.3389/fnins.2023.1321176.
35. Mondelli V., Vernon A.C. From early adversities to immune activation in psychiatric disorders: the role of the sympathetic nervous system. Clin Exp Immunol. 2019;197:319–28. https://doi.org/10.1111/cei.13351.
36. Zefferino R., Di Gioia S., Conese M. Molecular links between endocrine, nervous and immune system during chronic stress. Brain Behav. 2020;11:e01960. https://doi.org/10.1002/brb3.1960.
37. Gleason J.L., Drew L.B., Jones M.M. Stress, anxiety, and depression as precipitants of infertility: a comprehensive literature review. Womens Reprod Health. 2020;7(3):205–22. https://doi.org/10.1080/23293691.2020.1780397.
38. Schliep K.C., Mumford S.L., Vladutiu C.J. et al. Perceived stress, reproductive hormones, and ovulatory function: a prospective cohort study. Epidemiology. 2015;26(2):177–84. https://doi.org/10.1097/EDE.0000000000000238.
39. Shen L., Zhang W., Yuan Y. et al. Vaginal microecological characteristics of women in different physiological and pathological period. Front Cell Infect Microbiol. 2022;12:959793. https://doi.org/10.3389/fcimb.2022.959793.
40. Collins M.K., McCutcheon C.R., Petroff M.G. Impact of estrogen and progesterone on immune cells and host–pathogen interactions in the lower female reproductive tract. J Immunol. 2022;209(8):1437–49. https://doi.org/10.4049/jimmunol.2200454.
41. France M.T., Ma B., Gajer P. et al. VALENCIA: a nearest centroid classification method for vaginal microbial communities based on composition. Microbiome. 2020;8(1):166. https://doi.org/10.1186/s40168-020-00934-6.
42. France M., Alizadeh M., Brown S. et al. Towards a deeper understanding of the vaginal microbiota. Nat Microbiol. 2022;7(3):367–78. https://doi.org/10.1038/s41564-022-01083-2.
43. Lebedeva O.P., Popov V.N., Syromyatnikov M.Y. et al. Female reproductive tract microbiome and early miscarriages. APMIS. 2023;131(2):61–76. https://doi.org/10.1111/apm.13288.
44. Lebedeva O.P., Gryaznova M.V., Kozarenko O.N. et al. Vaginal microbiome in patients with menstrual cycle disorders (review). Research Results in Biomedicine. 2021;7(4):433–50. (In Russ.). https://doi.org/10.18413/2658-6533-2021-7-4-0-9.
45. Lebedeva O.P., Kalutsky P.V. Anti-infectious defense of vagina during use of low-dose monophasic contraceptives. Zhurnal mikrobiologii, epidemiologii i immunobiologi. 2007;(1):67–70. (In Russ.).
46. Dothard M.I., Allard S.M., Gilbert J.A. The effects of hormone replacement therapy on the microbiomes of postmenopausal women. Climacteric. 2023;26(3):182–92. https://doi.org/10.1080/13697137.2023.2173568.
47. Oliveira N.S.D., Lima A.B.F.D., Brito J.C.R.D. et al. Postmenopausal vaginal microbiome and microbiota. Front Reprod Health. 2022;3:780931. https://doi.org/10.3389/frph.2021.780931.
48. Bakhtiyarov K.R., Ignatko I.V., Zueva A.S. et al. The role of uterine and vaginal microbiome affecting the outcomes of assisted reproductive technologies. Obstetrics, Gynecology and Reproduction. 2025;19(2):273–81. (In Russ.). https://doi.org/10.17749/2313-7347/ob.gyn.rep.2025.592.
49. Tursunova N.B., Lebedeva O.P., Altukhova O.B., Nagorny A.V. An updated view on the role of the female reproductive tract microbiome in IVF outcomes. Obstetrics, Gynecology and Reproduction. 2023;17(4):512–25. (In Russ.). https://doi.org/10.17749/2313-7347/ob.gyn.rep.2023.433.
50. Gryaznova M., Kozarenko O., Smirnova Y. et al. Cervical and vaginal microbiomes in early miscarriages and ongoing pregnancy with and without dydrogesterone usage. Int J Mol Sci. 2023;24(18):13836. https://doi.org/10.3390/ijms241813836.
51. Goncharov A.E., Rischuk S.V., Aslanov B.I. et al. Features of microbiocenoses of various biotopes in women as potential miscarriage risk factor. Epidemiologiâ i vakcinoprofilaktika. 2021;20(5):107–14. (In Russ.). https://doi.org/10.31631/2073-3046-2021-20-5-107-114.
52. Megrabyan A.D., Ignatko I.V., Yakubova D.I., Baibulatova Sh. The role of abnormal vaginal microbiocenosis in increasing the risk of adverse reproductive outcome. Vrach. 2023;34(1):53–6. (In Russ.). https://doi.org/10.29296/25877305-2023-01-11.
53. Olenev A.S., Novikova V.A., Radzinsky V.E., Stetsyuk O. Intrapartum maternal risks of group B Streptococcus carriage in premature rupture of membranes. Zhurnal akusherstva i zhenskih boleznej. 2024;73(5):62–75. (In Russ.). https://doi.org/10.17816/jowd568825.
54. Nansel T.R., Riggs M.A., Yu K.F. et al. The association of psychosocial stress and bacterial vaginosis in a longitudinal cohort. Am J Obstet Gynecol. 2006;194(2):381–6. https://doi.org/10.1016/j.ajog.2005.07.047.
55. Culhane J.F., Rauh V., McCollum K.F. et al. Maternal stress is associated with bacterial vaginosis in human pregnancy. Matern Child Health J. 2001;5(2):127–34. https://doi.org/10.1023/A:1011305300690.
56. Turpin R., Slopen N., Borgogna J.L.C. et al. Perceived stress and molecular bacterial vaginosis in the national institutes of health longitudinal study of vaginal flora. Am J Epidemiol. 2021;190(11):2374–83. https://doi.org/10.1093/aje/kwab147.
57. Scheible K., Beblavy R., Sohn M.B. et al. Affective symptoms in pregnancy are associated with the vaginal microbiome. J Affect Disord. 2025;368:410–9. https://doi.org/10.1016/j.jad.2024.09.108.
58. Irving G., Miller D., Robinson A. et al. Psychological factors associated with recurrent vaginal candidiasis: a preliminary study. Sex Transm Infect. 1998;74(5):334. https://doi.org/10.1136/sti.74.5.334.
59. Ehrström S., Kornfeld D., Rylander E. Perceived stress in women with recurrent vulvovaginal candidiasis. J Psychosom Obstet Gynaecol. 2007;28(3):169–76. https://doi.org/10.1080/01674820601168176.
60. Moshfeghy Z., Tahari S., Janghorban R. et al. Association of sexual function and psychological symptoms including depression, anxiety and stress in women with recurrent vulvovaginal candidiasis. J Turk Ger Gynecol Assoc. 2020;21(2):90. https://doi.org/10.4274/jtgga.galenos.2019.2019.0077.
61. Thomas-White K., Navarro P., Wever F. et al. Psychosocial impact of recurrent urogenital infections: a review. Womens Health. 2023;19:17455057231216537. https://doi.org/10.1177/17455057231216537.
62. Ehrström S.M., Kornfeld D., Thuresson J., Rylander E. Signs of chronic stress in women with recurrent candida vulvovaginitis. Am J Obstet Gynecol. 2005;193(4):1376–81. https://doi.org/10.1016/j.ajog.2005.03.068.
63. Akimoto-Gunther L., Bonfim-Mendonça P.D.S., Takahachi G. et al. Highlights regarding host predisposing factors to recurrent vulvovaginal candidiasis: chronic stress and reduced antioxidant capacity. PLoS One. 2016;11(7):e0158870. https://doi.org/10.1371/journal.pone.0158870.
64. Jönsson P., Österberg K., Wallergård M. et al. Exhaustion-related changes in cardiovascular and cortisol reactivity to acute psychosocial stress. Physiol Behav. 2015;151:327–37. https://doi.org/10.1016/j.physbeh.2015.07.020.
65. Ives A.M., Bertke A.S. Stress hormones epinephrine and corticosterone selectively modulate herpes simplex virus 1 (HSV-1) and HSV-2 productive infections in adult sympathetic, but not sensory, neurons. J Virol. 2017;91(13):e00582-17. https://doi.org/10.1128/JVI.00582-17.
66. Goswami P., Ives A.M., Abbott A.R., Bertke A.S. Stress hormones epinephrine and corticosterone selectively reactivate HSV-1 and HSV-2 in sympathetic and sensory neurons. Viruses. 2022;14(5):1115. https://doi.org/10.3390/v14051115.
67. Jones C. Intimate relationship between stress and human alpha-herpes virus 1 (HSV-1) reactivation from latency. Curr Clin Microbiol Rep. 2023;10(4):236–45. https://doi.org/10.1007/s40588-023-00202-9.
68. Lu D., Sundström K., Sparén P., et al. Bereavement is associated with an increased risk of HPV infection and cervical cancer: an epidemiological study in Sweden. Cancer Res. 2016;76(3):643–51. https://doi.org/10.1158/0008-5472.CAN-15-1788.
69. Kuebler U., Fischer S., Mernone L. et al. Is stress related to the presence and persistence of oncogenic human papillomavirus infection in young women? BMC Cancer. 2021;21(1):419. https://doi.org/10.1186/s12885-021-08010-4.
70. DePunzio C., Salvestroni C., Guazzelli G. et al. Stress and cervical dysplasia. Eur J Gynaecol Oncol. 1998;19:287–90.
71. Coker A.L., Bond S., Madeleine M.M. et al. Psychosocial stress and cervical neoplasia risk. Biopsychosoc Sci Med. 2003;65(4):644–51. https://doi.org/10.1097/01.psy.0000041471.57895.08.
72. Fang C.Y., Miller S.M., Bovbjerg D.H. et al. Perceived stress is associated with impaired T-cell response to HPV16 in women with cervical dysplasia. Ann Behav Med. 2008;35(1):87–96. https://doi.org/10.1007/s12160-007-9007-6.
73. Pereira D.B., Antoni M.H., Danielson A. et al. Life stress and cervical squamous intraepithelial lesions in women with human papillomavirus and human immunodeficiency virus. Psychosom Med. 2003;65:427–34. https://doi.org/10.1097/01.PSY.0000041620.37866.89.
74. Lugović-Mihić L., Cvitanović H., Djaković I. et al. The influence of psychological stress on HPV infection manifestations and carcinogenesis. Cell Physiol Biochem. 2021;55(S2):71–88. https://doi.org/10.33594/000000395.
75. Cvitanović H., Milošević M., Bukvić-Bešlić I., Lugović-Mihić L. Determination of psychological stress, serum immune parameters, and cortisol levels in patients with human papilloma virus. Clin Ther. 2020;42(5):783–99. https://doi.org/10.1016/j.clinthera.2020.03.017.
76. Turpin R., Brotman R.M., Miller R.S. et al). Perceived stress and incident sexually transmitted infections in a prospective cohort. Ann Epidemiol. 2019;32:20–7. https://doi.org/10.1016/j.annepidem.2019.01.010.
77. Scheidell J.D., Thorpe L.E., Adimora A.A. et al. (2020). Perceived stress, sexually transmitted infection, and pelvic inflammatory disease: examination of differences in associations among black and white women. Sex Transm Dis. 2020;47(9):617–24. https://doi.org/10.1097/olq.0000000000001232.
78. Moreno I., Codoñer F.M., Vilella F. et al. Evidence that the endometrial microbiota has an effect on implantation success or failure. Am J Obstet Gynecol. 2016;215(6):684–703. https://doi.org/10.1016/j.ajog.2016.09.075.
79. Kyono K., Hashimoto T., Nagai Y. et al. Analysis of endometrial microbiota by 16S ribosomal RNA gene sequencing among infertile patients: a single-center pilot study. Reprod Med Biol. 2018;17(3):297–306. https://doi.org/10.1002/rmb2.12105.
80. Pelzer E.S., Willner D., Buttini M. et al. The fallopian tube microbiome: implications for reproductive health. Oncotarget. 2018;9(30):21541–59. https://doi.org/10.18632/oncotarget.25059.
81. Canha-Gouveia A., Di Nisio V., Salumets A. et al. The upper reproductive system microbiome: evidence beyond the uterus. Semin Reprod Med. 2023;41(5):190–9. https://doi.org/10.1055/s-0043-1778056.
82. Sola-Leyva A., Pérez-Prieto I., Di Nisio V. et al. Assessing the ovarian microbiome: lack of a distinguishable microbial signature beyond contamination. Reprod BioMedicine Online. 2025;51(3):104988. https://doi.org/10.1016/j.rbmo.2025.104988.
83. Pelzer E.S., Allan J.A., Cunningham K. et al. Microbial colonization of follicular fluid: alterations in cytokine expression and adverse assisted reproduction technology outcomes. Hum Reprod. 2011;26(7):1799–812. https://doi.org/10.1093/humrep/der108.
84. Huang T., Cao R., Liu P. et al. The severity of depression is associated with pelvic inflammatory diseases: A cross-sectional study of the United States National Health and Nutrition Examinations from 2013 to 2018. Front Med. 2022;9:926351. https://doi.org/10.3389/fmed.2022.926351.
85. Purewa S., Chapma S.C.E., van den Akker O.B.A. A systematic review and meta analysis of psychological predictors of successful assisted reproductive technologies. BMC Research Notes. 2017;10(1):711. https://doi.org/10.1186/s13104-017-3049-z.
86. Freestone P.P., Sandrini S.M., Haigh R.D., Lyte M. Microbial endocrinology: how stress influences susceptibility to infection. Trends Microbiol. 2008;16(2):55–64. https://doi.org/10.1016/j.tim.2007.11.005.
Review
For citations:
Tutova A.V., Lebedeva O.P., Kaluzhnova E.P., Chadyuk M.K., Kozarenko O.N., Kalashnikova I.V., Nagorny A.V., Selivanova A.V. Stress and microbiocenosis of the female reproductive tract. Obstetrics, Gynecology and Reproduction. (In Russ.) https://doi.org/10.17749/2313-7347/ob.gyn.rep.2026.808
JATS XML

This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.




































