Establishing the relationship between the growth stage of a pituitary tumor and visual functions using the area of the zone of chiasmal pressure from the tumor

Authors

  • K. S. Iegorova SI “Romodanov Neurosurgery Institute, National Academy of Medical Sciences of Ukraine”, Kyiv, Ukraine https://orcid.org/0000-0003-2801-3658
  • M. O. Guk SI “Romodanov Neurosurgery Institute, National Academy of Medical Sciences of Ukraine”, Kyiv, Ukraine
  • O. V. Ukrainets

DOI:

https://doi.org/10.31288/Ukr.j.ophthalmol.202616370

Keywords:

mathematical modeling, 3D modeling, pituitary adenoma, compressive optic neuropathy, optic chiasm, surface pressure area, optic neuropathy

Abstract

Purpose: To develop a mathematical model of chiasmal compression using a computer model of the area of surface pressure from the tumor.
Material and Methods: We reviewed the medical records of 361 patients treated for compressive optic neuropathy due to pituitary adenoma (PA) at SI “Romodanov Neurosurgery Institute, NAMS of Ukraine” in 2018-2024. Patients underwent clinical neurological and ophthalmological examinations, magnetic resonance imaging (MRI), computed tomography (CT) and functional studies. Mathematical modeling was done in cooperation with the Department of Software Engineering in Energy Industry, National Technical University of Ukraine “Igor Sikorsky Kyiv Polytechnic Institute”. The study was based on modeling and statistical analysis.
Results: Patients (54.7% were women and 45.3% were men; mean age, 54.3 ± 12.5 years) were divided into 3 groups: group 1, early stage (small PAs, n = 115), group 2, moderately advanced stage (moderate-size PAs, n = 157), and group 3, advanced stage (giant PAs, n = 89). The difference between groups was statistically significant (p < 0.05). The study has confirmed the efficacy of using both CT and MRI for assessing tumor size. A mathematical model (z = 377.38 + 122.19x – 2.25y – 77.74x² – 2.91xy + 0,02y²) was developed for predicting the area of pressure zone from a PA. Critical thresholds of the area of the zone of chiasmal pressure from a PA were determined. An especially abrupt decline in retinal nerve fiber layer (RNFL) thickness was noted as pressure zone area (PZA) exceeded 200 conventional units (CU), and the worst visual acuity (VA; 0.42) and RNFL thickness (40 µm) values were noted for a PZA of 300 CU.
Conclusion: The model proposed has some substantial advantages compared to those developed previously. It is based on a complex approach that combines clinical data from various diagnostic modalities with mathematical modeling. This allows taking in account multiple parameters such as PZA, VA and RNFL thickness. High model fitness (R² = 0.9910) and clear correlations between parameters provide for a reliable prediction of the PZA. This has an important practical value for detecting the pathology and planning the treatment strategy early.

Author Biographies

K. S. Iegorova, SI “Romodanov Neurosurgery Institute, National Academy of Medical Sciences of Ukraine”, Kyiv, Ukraine

Kateryna S. Iegorova, Cand Sc (Med), Senior Researcher, Ophthalmologist, Neuro-Ophthalmology Unit, SI “Romodanov Neurosurgery Institute, National Academy of Medical Sciences of Ukraine”, Kyiv, Ukraine

M. O. Guk, SI “Romodanov Neurosurgery Institute, National Academy of Medical Sciences of Ukraine”, Kyiv, Ukraine

Mykola O. Guk ,Neurosurgeon, Dr Sc (Med), Prof., and Chief Researcher, Department for Endonasal Cranial Base Endosurgery, SI “Romodanov Neurosurgery Institute, National Academy of Medical Sciences of Ukraine”, National Academy of Medical Sciences of Ukraine”, 040050, 32 P. Maiboroda St., Kyiv, Ukraine

O. V. Ukrainets

Oleksii V. Ukrainets, Neurosurgeon, PhD and Researcher, Department for Endonasal Cranial Base Endosurgery, SI “Romodanov Neurosurgery Institute, National Academy of Medical Sciences of Ukraine”, National Academy of Medical Sciences of Ukraine”, 040050, 32 P. Maiboroda St., Kyiv, Ukraine

References

1. Wang EW, Gardner PA, Zanation AM. International consensus statement on endoscopic skull-base surgery: executive summary. Int Forum Allergy Rhinol. 2019;9(S3):S127-S144. https://doi.org/10.1002/alr.22327

2. Asa SL, Mete O, Perry A, Osamura RY. Overview of the 2022 WHO Classification of Pituitary Tumors. Endocr Pathol. 2022;33(1):6-26. https://doi.org/10.1007/s12022-022-09703-7

3. Rutkowski MJ, Chang KE, Cardinal T, et al. Development and clinical validation of a grading system for pituitary adenoma consistency. J Neurosurg. 2020;134(6):1800-1807. Published 2020 Jun 5. https://doi.org/10.3171/2020.4.JNS193288

4. Westall SJ, Aung ET, Kejem H, Daousi C, Thondam SK. Management of pituitary incidentalomas. Clin Med (Lond). 2023;23(2):129-134.https://doi.org/10.7861/clinmed.2023-0020

5. Mete O, Cintosun A, Pressman I, Asa SL. Epidemiology and biomarker profile of pituitary adenohypophysial tumors. Mod Pathol. 2018;31(6):900-909. https://doi.org/10.1038/s41379-018-0016-8

6. Fleseriu M, Biller BMK, Freda PU, et al. A Pituitary Society update to acromegaly management guidelines. Pituitary. 2021;24(1):1-13. https://doi.org/10.1007/s11102-020-01091-7

7. Ntali G, Wass JA. Epidemiology, clinical presentation and diagnosis of non-functioning pituitary adenomas. Pituitary. 2018;21(2):111-118. https://doi.org/10.1007/s11102-018-0869-3

8. Mooney MA, Hardesty DA, Sheehy JP, et al. Rater Reliability of the Hardy Classification for Pituitary Adenomas in the Magnetic Resonance Imaging Era. J Neurol Surg B Skull Base. 2017;78(5):413-418. https://doi.org/10.1055/s-0037-1603649

9. Mattogno PP, Zoli M, D'Alessandris QG, et al. Ultra-Early Treatment of Neurosurgical Emergencies with Endoscopic Endonasal Approach: Experience from Three Italian Referral Centers. J Clin Med. 2023;12(17):5471. Published 2023 Aug 23. https://doi.org/10.3390/jcm12175471

10. Danesh-Meyer HV, Yoon JJ, Lawlor M, Savino PJ. Visual loss and recovery in chiasmal compression. Prog Retin Eye Res. 2019;73:100765. https://doi.org/10.1016/j.preteyeres.2019.06.001

11. McIlwaine GG, Carrim ZI, Lueck CJ, Chrisp TM. A mechanical theory to account for bitemporal hemianopia from chiasmal compression. J Neuroophthalmol. 2005;25(1):40-43. https://doi.org/10.1097/00041327-200503000-00011

12. Kosmorsky GS, Dupps WJ Jr, Drake RL. Nonuniform pressure generation in the optic chiasm may explain bitemporal hemianopsia. Ophthalmology. 2008;115(3):560-565. https://doi.org/10.1016/j.ophtha.2007.07.004

13. Wang X, Neely AJ, McIlwaine GG, Lueck CJ. Multi-scale analysis of optic chiasmal compression by finite element modelling. J Biomech. 2014;47(10):2292-2299. https://doi.org/10.1016/j.jbiomech.2014.04.040

14. Wang X, Neely AJ, McIlwaine GG, Tahtali M, Lillicrap TP, Lueck CJ. Finite element modeling of optic chiasmal compression. J Neuroophthalmol. 2014;34(4):324-330. https://doi.org/10.1097/WNO.0000000000000145

15. Wang X, Neely AJ, McIlwaine GG, Lueck CJ. Biomechanics of chiasmal compression: sensitivity of the mechanical behaviors of nerve fibers to variations in material property and geometry. Int J Comput Methods Eng Sci Mech 2016;17: 165-71. https://doi.org/10.1080/15502287.2015.1084069

16. Wang X, Neely AJ, Neeranjali S. Jain, Swaranjali V. Jain, Sanjiv Jain, Murat Tahtali, Gawn G. McIlwaine, Lueck CJ. Biomechanics of human optic chiasmal compression: ex vivo experiment and finite element modelling. Medicine in Novel Technology and Devices. 2022; 13:100113. https://doi.org/10.1016/j.medntd.2021.100113

Published

2026-02-26

How to Cite

[1]
Iegorova, K.S. et al. 2026. Establishing the relationship between the growth stage of a pituitary tumor and visual functions using the area of the zone of chiasmal pressure from the tumor. Ukrainian Journal of Ophthalmology . 1 (Feb. 2026), 63–70. DOI:https://doi.org/10.31288/Ukr.j.ophthalmol.202616370.

Issue

Section

Clinical Ophthalmology

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