Study of tear VEGF levels in glaucoma and hypertensive disorders of pregnancy
https://doi.org/10.53432/2078-4104-2026-25-1-3-9
Abstract
PURPOSE. To study the tear levels of vascular endothelial growth factor (VEGF) in glaucoma and hypertensive disorders of pregnancy.
METHODS. The study included 44 participants: 7 pregnant women with an uncomplicated physiological pregnancy, 12 patients diagnosed with moderate (8 women) and severe (4 women) preeclampsia, 19 pregnant patients with stage I–II chronic arterial hypertension; the comparison group consisting of 6 patients with advanced primary open-angle glaucoma hospitalized for surgical treatment due to uncompensated intraocular pressure. After standard ophthalmologic and obstetric examinations, tear samples were collected using an original sampling technique for analysis.
RESULTS. Tear VEGF levels were significantly higher in the preeclampsia group, in pregnant women with chronic arterial hypertension, and in patients with glaucoma compared with those with physiological pregnancy. Moreover, the indicator was higher in preeclampsia than in arterial hypertension. No statistically significant differences were found when comparing the preeclampsia and glaucoma groups.
CONCLUSION. Tear VEGF levels are significantly elevated in preeclampsia and glaucoma. Tear VEGF level shows significant differences between physiological pregnancy and pregnancy complicated by chronic arterial hypertension. Investigation of tear VEGF levels appears promising for both ocular and systemic pathology.
About the Authors
T. Yu. MatnenkoRussian Federation
Matnenko T.Yu., Cand. Sci. (Med.), Associate Professor, Associate Professor at the Academic Department of Ophthalmology
12 Lenina St., Omsk, 644099
O. I. Lebedev
Russian Federation
Lebedev O.I., Dr. Sci. (Med.), Professor, Dean of the Faculty of General Medicine, Head of the Academic Department of Ophthalmology
12 Lenina St., Omsk, 644099
S. V. Barinov
Russian Federation
Barinov S.V., Dr. Sci. (Med.), Professor, Head of the Academic Department of Obstetrics and Gynecology № 2
12 Lenina St., Omsk, 644099
A. N. Zolotov
Russian Federation
Zolotov A.N., Cand. Sci. (Med.), Associate Professor, Senior Researcher at the Central Research Laboratory,
Associate Professor at the Academic Department of Pathophysiology
12 Lenina St., Omsk, 644099
Yu. I. Chulovsky
Russian Federation
Chulovsky Yu.I., Cand. Sci. (Med.), Associate Professor, Associate Professor at the Academic Department of Obstetrics and Gynecology № 2
12 Lenina St., Omsk, 644099
D. G. Novikov
Russian Federation
Novikov D.G., Cand. Sci. (Med.), Associate Professor, Associate Professor of the Academic Department of Clinical Laboratory Diagnostics of Additional Professional Education, Head of the Central Research Laboratory
12 Lenina St., Omsk, 644099
N. A. Kirichenko
Russian Federation
Kirichenko N.A., Assistant Professor at the Academic Department of Clinical Laboratory Diagnostics of Additional Professional Education, junior researcher at the Central Research Laboratory
12 Lenina St., Omsk, 644099
I. V. Petrovskaya
Russian Federation
Petrovskaya I.V., resident physician at the Academic Department of Ophthalmology
12 Lenina St., Omsk, 644099
References
1. Vlasov T.D., Nesterovich I.I., Shimanski D.A. Endothelial dysfunction: from the particular to the general. Return to the "old paradigm"? Regional blood circulation and microcirculation 2019; 18(2):19-27. https://doi.org/10.24884/1682-6655-2019-18-2-19-27
2. Apte R.S., Chen D.S., Ferrara N. VEGF in Signaling and Disease: Beyond Discovery and Development. Cell 2019; 176(6):1248-1264. https://doi.org/10.1016/j.cell.2019.01.021
3. Brash J.T., Ruhrberg C., Fantin A. Evaluating VEGF-Induced Vascular Leakage Using the Miles Assay. Methods Mol Biol 2022; 2475:289-295. https://doi.org/10.1007/978-1-0716-2217-9_21.
4. Nawaz M., Heydarkhan-Hagvall S., Tangruksa B., González-King Garibotti H. et al. Lipid Nanoparticles Deliver the Therapeutic VEGFA mRNA In Vitro and In Vivo and Transform Extracellular Vesicles for Their Functional Extensions. Adv Sci (Weinh) 2023; 10(12):e2206187. https://doi.org/10.1002/advs.202206187.
5. Islamgaleeva Z.M., Khusainova L.N., Mingazetdinova L.N., Mutalova E.G. Evaluation of endothelial dysfunction and angiogenesis in hypertensive patients with metabolic syndrome. Modern problems of science and education 2015; 5:123.
6. Ba J., Peng R.S., Xu D., Li Y.H. et al. Intravitreal anti-VEGF injections for treating wet agerelated macular degeneration: a systematic review and meta-analysis. Drug Des Devel Ther 2015; 9:5397-5405. https://doi.org/10.2147/DDDT.S86269.
7. Tikhonovich M.V., Iojleva E.E. The role of vascular endothelial growth factor in retinal physiology. Vestnik of the Orenburg State University 2015; 12(187):244-249.
8. Kirilenko M.Y., Tikunova E.V., Sirotina S.S., Polonikov A.V. et al. Studying the association between genetic polymorphism of growth factors and the development of primary open-angle glaucoma. Russian Annals of Ophthalmology 2017; 133(3):9-15. https://doi.org/0.17116/oftalma201713339-15
9. Tul'tseva S.N., Titarenko A.I., Rukhovets A.G. Hemodynamic changes in ischemic venous occlusion in young adults. Current issues in medicine in modern conditions: a collection of scientific papers from an international scientific and practical conference. Nizhnii Novgorod, 2016:34-36.
10. Fateeva V.V., Vorob'eva O.V. Cerebral markers of endothelial dysfunction in chronic brain ischemia. S.S. Korsakov’s Journal of Neurology and Psychiatry 2017; 117(4):107-111. https://doi.org/10.17116/jnevro201711741107-111
11. Mandić J.J., Kozmar A., Kusačić-Kuna S., Jazbec A. et al. The levels of 12 cytokines and growth factors in tears: hyperthyreosis vs euthyreosis. Graefes Arch Clin Exp Ophthalmol 2018; 256(4):845-852. https://doi.org/10.1007/s00417-017-3892-6.
12. Tomečková V., Tkáčiková S., Talian I., Fabriciová G. et al. Experimental Analysis of Tear Fluid and Its Processing for the Diagnosis of Multiple Sclerosis. Sensors (Basel) 2023; 23(11):5251. https://doi.org/10.3390/s23115251.
13. Khanna R.K., Catanese S., Emond P., Corcia P. et. al. Metabolomics and lipidomics approaches in human tears: A systematic review. Surv Ophthalmol 2022; 67(4):1229-1243. https://doi.org/10.1016/j.survophthal.2022.01.010.
14. Shabrov A.V., Apresyan A.G., Dobkes A.L., Ermolov S.U. et al. Current methods of endothelial dysfunction assessment and their possible use in the practical medicine. Rational Pharmacotherapy in Cardiology 2016; 12(6):733-742.
15. Neroev V.V., Zaytseva O.V., Balatskaya N.V., Kurchaeva Z.V. Local and systemic VEGF-А production in complicated proliferative diabetic retinopathy. Medical Immunology (Russia) 2016; 18(4):357-364.
16. Budzinskaya M.V., Lipatov D.V., Pavlov V.G., Petrachkov D.V. Biomarkers for diabetic retinopathy. Diabetes Mellitus (Russia) 2020; 23(1):88-94. https://doi.org/10.14341/DM10045
17. Shahidatul-Adha M., Zunaina E., Aini-Amalina M.N. Evaluation of vascular endothelial growth factor (VEGF) level in the tears and serum of age-related macular degeneration patients. Sci Rep 2022; 12(1):4423.
18. Hang H., Yuan S., Yang Q., Yuan D. et al. Multiplex bead array assay of plasma cytokines in type 2 diabetes mellitus with diabetic retinopathy. Mol Vis 2014; 20:1137-1145.
19. Chen Y., Zhang Z. Placenta related pathogenic factors for preeclampsia. Open J Obstet Gynecol 2012; 2(4):340-345.
20. Sakvarelidze N.Y., Tsakhilovа S.G., Muradova V.S., Zharkov N.V. et al. Fetoplacental Angiogenesis in Preeclampsia. Clinical and Morphological Aspects. Effective pharmacotherapy 2020; 16(28):6-11.
21. Fomin N.E., Kuroyedov A.V. Markers of vascular autoregulation in primary open-angle glaucoma. Russian Journal of Clinical Ophthalmology 2019; 19(4):218-223.
22. Drozdova E.A., Khokhlova D.Y., Mezentseva E.A., Nikushkina K.V. Studies of systemic and local cytokine level in retinal vein occlusion associated with antiangiogenic therapy. Medical Immunology (Russia) 2018; 3(20):365-372.
23. Dzhidzhikhiya K.M., Sinyavtseva V.K., Dzhidzhikhiya Z.M., Vekua D.G. et al. Endothelial dysfunction in pathogenesis of arterial hypertension in metabolic syndrome. Mezhdunarodnyi zhurnal eksperimental'nogo obrazovaniya 2013; 11-3:261-262.
24. Hussain N., Sher S.F., Lin X., Adil M. Association of VEGF Gene Polymorphism (rs699947) with Glaucoma and In-Silico Study of Antiglaucoma Bioactive Compounds. Appl Biochem Biotechnol 2022; 194:5185-5195. https://doi.org/10.1007/s12010-022-04014-3.
25. Dimtsas G.S., Tsiogka A., Moschos M.M. VEGF levels in the aqueous humor of patients with primary open angle glaucoma: A systematic review and a meta-analysis. Eur J Ophthalmol 2023; 33(6):2228-2235. https://doi.org/10.1177/11206721231168146.
26. Zhang Q., Gu L., Xu Y. Analysis of the relationship between VEGF, NLRP3 inflammatory complex, EPO levels, and ocular hemodynamics in patients with primary open-angle glaucoma. BMC Ophthalmol 2024; 24(1):331. https://doi.org/10.1186/s12886-024-03600-9.
27. Malisheva J.V., Iureva T.N., Volkova N.V., Kursakova J.V. et al. Prospective assessment of cytokines and regulatory proteins concentration in the tear fluid of POAG patients with various hypotensive effects after non-penetrating deep sclerectomy. Acta Biomedica Scientifica 2023; 8(2):170-178.
Review
For citations:
Matnenko T.Yu., Lebedev O.I., Barinov S.V., Zolotov A.N., Chulovsky Yu.I., Novikov D.G., Kirichenko N.A., Petrovskaya I.V. Study of tear VEGF levels in glaucoma and hypertensive disorders of pregnancy. National Journal glaucoma. 2026;25(1):3-19. (In Russ.) https://doi.org/10.53432/2078-4104-2026-25-1-3-9
JATS XML

















