Comparison of Insulin-Like Growth Factor-1 (IGF-1) and Transforming Growth Factor-β1 (TGF-β1) Protein Expression Between Patients with Pelvic Organ Prolapse With and Without Cervical Elongation
Abstract
Objective: Pelvic organ prolapse (POP) is a condition caused by weakened pelvic support structures and is often associated with cervical elongation. The role of growth factors, particularly insulin-like growth factor-1 (IGF-1) and transforming growth factor-β1 (TGF-β1), in the pathogenesis of cervical elongation remains unclear.
Methods: This study was conducted at Dr. Hasan Sadikin General Hospital, Bandung, involving patients with pelvic organ prolapse with or without cervical elongation selected by consecutive sampling. Cervical IGF-1 and TGF-β1 expression was assessed by immunohistochemistry, and prolapse severity by POP-Q. Each group included 23 subjects. Data were analyzed using the Shapiro–Wilk and Mann–Whitney U tests.
Results: Most participants were ≥ 50 years old, and the POP without cervical elongation group had a significantly higher proportion of postmenopausal women (95.7% vs. 65.2%; p = 0.02). IGF-1 expression did not differ significantly between the two groups (mean 6.39 vs. 7.01; p>0.05). In contrast, TGF-β1 expression was significantly lower in the POP with cervical elongation group than in the POP without cervical elongation group (2.62 ± 1.08 vs. 5.48 ± 2.41; p < 0.001).
Conclusion: Decreased TGF-β1 expression may contribute to cervical elongation in POP through impaired extracellular matrix remodeling, while IGF-1 does not clearly distinguish this phenotype. These findings suggest cervical elongation as a distinct biological entity within the POP spectrum, with implications for its pathophysiology and surgical management.
Perbandingan Ekspresi Protein Insulin-Like Growth Factor-1 (IGF-1) dan Transforming Growth Factor-β1 (TGF-β1) antara Pasien Prolaps Organ Panggul dan tanpa Elongasi Serviks
Abstrak
Tujuan: Prolaps organ panggul (POP) merupakan kondisi akibat kelemahan jaringan penunjang pelvis yang sering disertai elongasi serviks. Peran growth factor, khususnya insulin-like growth factor-1 (IGF-1) dan transforming growth factor-β1 (TGF-β) dalam patogenesis elongasi serviks belum sepenuhnya dipahami.
Metode: Penelitian ini dilakukan di RSUP Dr. Hasan Sadikin Bandung dengan melibatkan pasien prolaps organ panggul dengan atau tanpa elongasi serviks yang dipilih secara consecutive sampling. Ekspresi IGF-1 dan TGF-β1 pada jaringan serviks dinilai menggunakan imunohistokimia, sedangkan derajat prolaps dinilai dengan sistem POP-Q. Masing-masing kelompok terdiri dari 23 subjek. Data dianalisis menggunakan uji Shapiro–Wilk dan Mann–Whitney U.
Hasil: Sebagian besar subjek berusia ≥50 tahun, dengan proporsi menopause lebih tinggi pada kelompok POP tanpa elongasi serviks dibandingkan kelompok POP dengan elongasi serviks (95,7% vs. 65,2%; p=0,02). Tidak terdapat perbedaan bermakna pada ekspresi IGF-1 antara kedua kelompok (6,39 vs. 7,01; p>0,05). Sebaliknya, ekspresi TGF-β1 secara signifikan lebih rendah pada kelompok POP dengan elongasi serviks dibandingkan dengan kelompok POP tanpa elongasi serviks (2,62 ± 1,08 vs. 5,48 ± 2,41; p < 0,001).
Kesimpulan: Penurunan ekspresi TGF-β1 dapat berkontribusi terhadap elongasi serviks pada POP melalui gangguan remodeling matriks ekstraseluler, sedangkan IGF-1 tidak secara jelas membedakan fenotipe ini. Temuan ini menunjukkan bahwa elongasi serviks merupakan entitas biologis tersendiri dalam spektrum POP, dengan implikasi terhadap patofisiologi dan tata laksana bedah.
Keywords
Full Text:
PDFReferences
Hadizadeh-Talasaz Z, Khadivzadeh T, Mohajeri T, Sadeghi M. Worldwide Prevalence of Pelvic Organ Prolapse: A Systematic Review and Meta-Analysis.
Nosti PA, Gutman RE, Iglesia CB, Park AJ, Tefera E, Sokol AI. Defining Cervical Elongation: A Prospective Observational Study. J Obstet Gynaecol Can. 2017;39(4):223–8.
Pb H, Bansal N, Hiremath R. Extreme cervical elongation. Int J Reprod Contracept Obstet Gynecol. 2014;777–9.
Yoshida K, Jayyosi C, Lee N, Mahendroo M, Myers KM. Mechanics of cervical remodelling: insights from rodent models of pregnancy. Interface Focus. 2019 Oct 6;9(5):20190026.
Hao J, Yao W, Harris WBR, Vink JY, Myers KM, Donnelly E. Characterization of the collagen microstructural organization of human cervical tissue. Reproduction. 2018 Jul;156(1):71–9.
Carroll L, O’ Sullivan C, Doody C, Perrotta C, Fullen B. Pelvic organ prolapse: The lived experience. Laganà AS, editor. PLoS ONE. 2022 Nov 2;17(11):e0276788.
Yin Y, Han Y, Shi C, Xia Z. IGF-1 regulates the growth of fibroblasts and extracellular matrix deposition in pelvic organ prolapse. Open Med (Wars). 2020 Sep 2;15(1):833–40.
Alvilusia A, Fauzi A, Azhari A, Wresnindyatsih W, Saleh I. Transforming Growth Factor β1 and Tropoelastin Expression in Uterine Prolapse. Indones J Obstet Gynecol. 2016 Oct 14;70.
Zhao Y, Xia Z, Lin T, Qin M. Transforming Growth Factor Beta 1 and p44/42 Expression in Cardinal Ligament Tissues of Patients with Pelvic Organ Prolapse. Med Sci Monit. 2021 Mar 24;27.
Praharsini K, Sasotya S, Suakarsa MRA. Comparison of IGF-1 protein expression as a Marker for Type I Collagen production in the Uterosacral ligament of patients with uterine prolapse and without uterine prolaps to prevent uterine prolaps. Ind Journal of Obstetrics and Gynecology Science. 2025 Mar 74-81.
Brown HW, Hegde A, Huebner M, Neels H, Barnes HC, Marquini GV, et al. International urogynecology consultation chapter 1 committee 2: Epidemiology of pelvic organ prolapse: prevalence, incidence, natural history, and service needs. Int Urogynecol J. 2022;33:173–87.
Liu YY, Wang CL, Loo ZX, Lin KL, Long CY. Clinical Risk Factors for Uterine Cervical Elongation among Women with Pelvic Organ Prolapse. Int J Environ Res Public Health. 2021 Sep 2;18(17):9255.
Tondro Anamag F, Noshad Iran L, Mousavi S, Salehi‐Pourmehr H, Bastani P. Comparison of cervical length measured by pelvic organ prolapse quantification system and sonography. Sonography. 2025;12:54–9.
Xie X, Shen J. Analysis of Risk Factors of Pelvic Organ Prolapse in Postmenopausal Women and Construction of Prediction Model. Altern Ther Health Med. 2024;30:265–9.
Rui B, Rui G, Yang Y. Unveiling pathogenesis of pelvic organ prolapse through transcriptomic and bioinformatic analyses in uterosacral ligament tissues of postmenopausal women. Front Genet. 2025;16:1588278.
Wu X, Liu X, Li T. Potential molecular targets for intervention in pelvic organ prolapse. Front Med. 2023 Sep 5;10:1158907.
Kong L, Wei L, Wang L, Geng M, Wang W, Liu X. IGF-1 regulates LARP6-mediated collagen metabolism in vaginal fibroblasts of POP patients via the PI3K/AKT pathway. Sci Rep. 2025;15:21977.
Xu H, Wang G, Li Q, Wang X, Xu D. Expressions of IGF-1, pAKT, and pS6 in Uterosacral Ligaments of Patients with Pelvic Organ Prolapse. Int Urogynecol J. 2025;36:1523–31.
Zhou Q, Li G, Kiley JX, Ogola B, Danso EK, Baiamonte LB, et al. Vaginal biomechanical function in premenopausal and postmenopausal women with and without pelvic organ prolapse. Sci Rep. 2025;15:27039.
Guler Z, Roovers JP. Role of Fibroblasts and Myofibroblasts on the Pathogenesis and Treatment of Pelvic Organ Prolapse. Biomolecules. 2022;12:94.
Liu C, Wang Y, Li BS, Yang Q, Tang JM, Min J, et al. Role of transforming growth factor β-1 in the pathogenesis of pelvic organ prolapse: A potential therapeutic target. International Journal of Molecular Medicine. 2017;40:347–56.
Sugaya K, Kadekawa K, Ashitomi K, Nishijima S, Matsumoto S. Plasma Levels of Transforming Growth Factor-Beta 1 in Women with Pelvic Organ Prolapse. OJU. 2023;13:133–42.
Du H, Yang M, Qi X, Yang L, Wang Z, Yang T, et al. Comprehensive Analysis of the Biomechanical Research of Pelvic Organ Prolapse: A Scientometric Approach. JMDH. 2025;Volume 18:1249–68.
Jameson SA, Swaminathan G, Dahal S, Couri B, Kuang M, Rietsch A, et al. Elastin homeostasis is altered with pelvic organ prolapse in cultures of vaginal cells from a lysyl oxidase‐like 1 knockout mouse model. Physiol Rep. 2020 Jun;8(11).
DOI: http://dx.doi.org/10.24198/obgynia.v9i2.1164
Refbacks
- There are currently no refbacks.

This work is licensed under a Creative Commons Attribution-ShareAlike 4.0 International License.
_CROSREF22.jpg)









