Окиснювальний баланс у фолікулярній рідині яєчників: кореляція з гормональним профілем та відповіддю яєчників у циклах екстракорпорального запліднення
Основний зміст сторінки статті
Анотація
The objective: to evaluate the oxidation-reduction potential (ORP) of follicular fluid (FF) in ovaries as a biomarker of the intrafollicular microenvironment and its association with oocyte maturation and in vitro fertilization (IVF) outcomes.
Materials and methods. A retrospective analysis of 212 IVF cycles during 2020–2023 was conducted. ORP in FF was measured using MiOXSYS. The concentrations of follicle-stimulating hormone (FSH), luteinizing hormone (LH), estradiol, anti-Müllerian hormone and prolactin were measured in blood serum. Correlations between ORP and gonadotropin levels, stimulation parameters, and oocyte outcomes were assessed.
Results. The mean ORP value in FF was 86.42 ± 23.23 mV, with wide interindividual variations. Weak but statistically significant positive correlations were observed between ORP and baseline FSH (ρ = 0.166, p = 0.016) and LH levels (ρ = 0.148, p = 0.032). Patients with basal FSH ≥ 8 IU/L exhibited higher ORP levels compared to women with FSH concentration < 8 IU/L (median 93.26 mV vs 81.70 mV, p = 0.041). However, ORP values did not differ significantly between groups stratified by total FSH dose, estradiol levels on chorionic gonadotropin day, or total number of retrieved oocytes. Notably, patients achieving ≥ 12 mature oocytes had a significantly higher oocyte maturation rate (86.19% vs 77.78%, p < 0.001), although their median ORP values were not significantly different (84.17 mV vs 89.68 mV, p = 0.849).
Conclusions. ORP in FF reflects subtle endocrine influences but was not directly predictive of oocyte number or maturity. Stable ORP values together with optimal stimulation (≥ 12 mature oocytes) were associated with better oocyte maturation, suggesting ORP as a potential marker of follicular health in IVF.
Блок інформації про статтю

Ця робота ліцензується відповідно до Creative Commons Attribution 4.0 International License.
Автори зберігають авторське право, а також надають журналу право першого опублікування оригінальних наукових статей на умовах ліцензії Creative Commons Attribution 4.0 International License, що дозволяє іншим розповсюджувати роботу з визнанням авторства твору та першої публікації в цьому журналі.
Посилання
Chaika OO. Analysis of somatic and reproductive history in patients with prognostically poor response of the testicles to gonadotropin stimulation. Reprod HealhWoman. 2021;(9):42-7. doi: 10.30841/2708-8731.9-10.2021.252589.
Hood RB, Liang D, Tan Y, Ford JB, Souter I, Chavarro JE, et al. Serum and follicular fluid metabolome and markers of ovarian stimulation. Hum Reprod. 2023;38(11):2196-207. doi: 10.1093/humrep/dead189.
Ilhan G, Bacanakgil BH, Vuruşkan AK, Eken MK, Karasu AFG, Bilgiç BE, et al. The effect of individual oocyte matched follicular fluid oxidant, antioxidant status, and pro-and anti-inflammatory cytokines on IVF outcomes of patients with diminished ovarian reserve. Med (Baltimore). 2023;102(4):E32757. doi: 10.1097/MD.0000000000032757.
Safarova AF. The role of clinical and immunological factors in the outcomes of in vitro fertilization procedure in women. Reprod Healh Woman. 2023;(3):2023. doi: 10.30841/2708-8731.7.2023.292603.
Tumanova L, Kolomiets O. Therapeutic options for pre-gravidary training in women with a history of combined infertility. Reprod Healh Woman. 2022;(2):53-8. doi: 10.30841/2708-8731.2.2022.261808.
Berestovyy OO. The ovulation stimulation in women with breast pathology and menstrual disorders of endocrine genesis. Reprod Healh Woman. 2020;(4):31-5. doi: 10.30841/2708-8731.4.2020.222142.
Pacella L, Zander-Fox DL, Armstrong DT, Lane M. Women with reduced ovarian reserve or advanced maternal age have an altered follicular environment. Fertil Steril. 2012;98(4):986-94.e1-2. doi: 10.1016/j.fertnstert.2012.06.025.
Perkhulyn OM, Pakharenko LV. Cervical elastograhy in patients with cervical insufficiency and a history of anovulatory infertility. Reprod Healh Woman. 2021;(3):34-6. doi: 10.30841/2708-8731.3.2021.234240.
Zec I, Goldštajn MŠ, Kuna K, Mikuš M, Stabile G, Bianco B, et al. Oxidative homeostasis in follicular fluid and reproductive outcomes – from bench to bedside. Prz Menopauzalny. 2022;21(4):276-84. doi: 10.5114/pm.2022.124019.
Al-Saleh I, Coskun S, Al-Rouqi R, Al-Rajudi T, Eltabache C, Abduljabbar M, et al. Oxidative stress and DNA damage status in couples undergoing in vitro fertilization treatment. Reprod Fertil. 2021;2(2):117-39. doi: 10.1530/RAF-20-0062.
Kumar S, Mishra V, Thaker R, Gor M, Perumal S, Joshi P, et al. Role of environmental factors & oxidative stress with respect to in vitro fertilization outcome. Indian J Med Res. 2018;148:S125-33. doi: 10.4103/ijmr.IJMR_1864_17.
Yilmaz N, Uygur D, Dogan M, Ozgu E, Salman B, Mollamahmutoglu L. The effect of follicular antimullerian hormone levels of non-obese, non-hyperandrogenemic polycystic ovary syndrome patients on assisted reproduction outcome. Gynecol Endocrinol. 2012;28(3):162-5. doi: 10.3109/09513590.2011.593667.
Kesari KK, Roychoudhury S, editors. Oxidative stress and toxicity in reproductive biology and medicine: A comprehensive update on male infertility. Vol. 1358. In: Advances in Experimental Medicine and Biology. Springer International Publishing; 2022. 379 p.
Sallam N, Hegab M, Mohamed F, El-Kaffash D. Effect of oxidative stress in semen, follicular fluid and embryo culture medium on the outcome of assisted reproduction. Al-Azhar Int Med J. 2021;2(7):59-65. doi: 10.21608/aimj.2021.79536.1495.
Nishihara T, Matsumoto K, Hosoi Y, Morimoto Y. Evaluation of antioxidant status and oxidative stress markers in follicular fluid for human in vitro fertilization outcome. Reprod Med Biol. 2018;17(4):481-6. doi: 10.1002/rmb2.12229.
Lin N, van Zomeren KC, Plosch T, Hofsink N, van Veen T, Li HT, et al. Follicle-stimulating hormone stimulates free radical generation without inducing substantial oxidative stress in human granulosa cells. Hum Reprod Open. 2025;2025(2):hoaf007. doi: 10.1093/hropen/hoaf007.
ESHRE Special Interest Group of Embryology and Alpha Scientists in Reproductive Medicine. The Vienna consensus: report of an expert meeting on the development of ART laboratory performance indicators. Reprod Biomed Online. 2017;35(5):494-510. doi: 10.1016/j.rbmo.2017.06.015.
Yu L, Liu M, Xu S, Wang Z, Liu T, Zhou J, et al. Follicular fluid steroid and gonadotropic hormone levels and mitochondrial function from exosomes predict embryonic development. Front Endocrinol (Lausanne). 2022;13:1025523. doi: 10.3389/fendo.2022.1025523.
Pizarro BM, Cordeiro A, Reginatto MW, Campos SPC, Mancebo ACA, Areas PCF, et al. Estradiol and progesterone levels are related to redox status in the follicular fluid during in vitro fertilization. J Endocr Soc. 2020;4(7):bvaa064. doi: 10.1210/jendso/bvaa064.
Pakharenko LV, Zhylka NY, Shcherbinska OS, Kravchuk IV, Lasytchuk OM, Zhurakivskyi VM, et al. The modern pathogenetic challenges of polycystic ovary syndrome. Reprod Healh Woman. 2024;(2):75-80. doi: 10.30841/2708-8731.2.2024.304662.
Duraker R, Guvendag Guven ES, Dilbaz S, Mentese A, Aydın S, Guven S. Oxidative stress status in severe OHSS patients who underwent long agonist protocol intracytoplasmic sperm injection cycles. Clin Exp Obstet Gynecol. 2021;48(2):312-6. doi: 10.31083/j.ceog.2021.02.5507.
Artini PG, Scarfò G, Marzi I, Fusi J, Obino ME, Franzoni F, et al. Oxidative stress-related signaling pathways predict oocytes’ fertilization in vitro and embryo quality. Int J Mol Sci. 2022;23(21):13442. doi: 10.3390/ijms232113442.
Ruan LL, Lv XY, Hu YL, Chen MX, Jing-Tang, Zhong ZH, et al. Metabolic landscape and pathogenic insights: a comprehensive analysis of high ovarian response in infertile women undergoing in vitro fertilization. J Ovarian Res. 2024;17(1):105. doi: 10.1186/s13048-024-01411-6.
Wang Y, Yi YC, Guu HF, Chen YF, Kung HF, Chang JC, et al. GnRH agonist-only trigger, compared to dual trigger, reduces oocyte retrieval rate in high responders without affecting cumulative live birth rate. Front Endocrinol (Lausanne). 2024;15:1-8. doi: 10.3389/fendo.2024.1461317.
Babayev E, Duncan FE. Age-associated changes in cumulus cells and follicular fluid: the local oocyte microenvironment as a determinant of gamete quality. Biol Reprod. 2022;106(2):351-65. doi: 10.1093/biolre/ioab241.
Becatti M, Fucci R, Mannucci A, Barygina V, Mugnaini M, Criscuoli L, et al. A biochemical approach to detect oxidative stress in infertile women undergoing assisted reproductive technology procedures. Int J Mol Sci. 2018;19(2):592. doi: 10.3390/ijms19020592.
Zaha I, Muresan M, Tulcan C, Huniadi A, Naghi P, Sandor M, et al. The role of oxidative stress in infertility. J Pers Med. 2023;13(8):1264. doi: 10.3390/jpm13081264.



