Proinflammatory humoral factors and their role in the pathogenesis of left ventricular hypertrophy in hypertension (literature review)

Authors

DOI:

https://doi.org/10.15587/2519-4798.2026.361623

Keywords:

arterial hypertension, chronic low-grade systemic inflammation, pro-inflammatory humoral factors, left ventricular hypertrophy, diastolic dysfunction, myocardial fibrosis, prediction of cardiovascular complications

Abstract

The aim of the research was to consider the role of chronic low-grade systemic inflammation and a list of pro-inflammatory factors (interleukins, chemokines, tumor necrosis factor alpha, adipocytokines, metalloproteinases and their inhibitors, growth and inflammatory factors, etc.) as predictors of the onset and progression of left ventricular hypertrophy and myocardial fibrosis in individuals with hypertension

Materials and Methods: keywords search of native and foreign sources of literature from scientometric databases Google Scholar, Clarivate, Web of Science, Scopus, PubMed and its analysis, considering data from modern European and Ukrainian guidelines of recent years was performed.

Results and Discussion. Data on the conditional classification of pro-inflammatory and anti-inflammatory cytokines, their activity in hypertensive heart and diastolic dysfunction, a number of traditional pro-inflammatory factors from the superfamilies of interleukins, pentraxins and transforming growth factor beta 1 are considered, as well as new promising biomolecules that are used as indicators of chronic low-grade systemic inflammation, including the experiments on hypertensive animals. The question of the prospects of using a multi-indicator model of pro-inflammatory factors in individuals with arterial hypertension is considered, a brief description of promising targeted therapeutic approaches to inhibit pro-inflammatory mechanisms in patients with is given.

Conclusions. In the research works of the last 10 years, a high scientific interest in the pathogenetically significant role of chronic low-grade systemic inflammation, pro-inflammatory factors in the occurrence and progression of hypertensive heart disease and left ventricular hypertrophy has revealed, and the promise of using biomarkers as their indicators for further personalized treatment on this basis for this category of patients has proven

Author Biographies

Dmytro Myloslavskyi, L. T. Mala Therapy National Institute of the National Academy of Medical Sciences of Ukraine

Candidate of Medical Sciences, Senior Researcher

Department of Arterial Hypertension and Prevention of Its Complications

Sergiy Koval, L. T. Mala Therapy National Institute of the National Academy of Medical Sciences of Ukraine

Doctor of Medical Sciences, Professor, Head of Department

Department of Arterial Hypertension and Prevention of Its Complications

Olga Mysnychenko, L. T. Mala Therapy National Institute of the National Academy of Medical Sciences of Ukraine

Candidate of Medical Sciences, Senior Researcher

Department of Arterial Hypertension and Prevention of Its Complications

Olga Lytvynova, National University of Pharmacy

Doctor of Medical Sciences, Professor

Department of Laboratory Diagnostics

Olena Shcheniavska, L. T. Mala Therapy National Institute of the National Academy of Medical Sciences of Ukraine

Scientific Researcher

Laboratory of Immuno-Biochemical and Molecular Genetic Research

References

  1. Mancia, G., Kreutz, R., Brunström, M., Burnier, M., Grassi, G., Januszewicz, A. et al. (2023). 2023 ESH Guidelines for the management of arterial hypertension The Task Force for the management of arterial hypertension of the European Society of Hypertension. Journal of Hypertension, 41 (12), 1874–2071. https://doi.org/10.1097/hjh.0000000000003480
  2. Cuspidi, C., Facchetti, R., Gherbesi, E., Quarti-Trevano, F., Vanoli, J., Mancia, G., Grassi, G. (2024). Ambulatory Blood Pressure Phenotypes, Arterial Stiffness, and Cardiac Remodeling. American Journal of Hypertension, 37 (12), 978–986. https://doi.org/10.1093/ajh/hpae106
  3. Chen, Y.-L., Wang, J.-G. (2023). Blood Pressure Variability and Left Ventricular Diastolic Dysfunction. American Journal of Hypertension, 37 (3), 163–164. https://doi.org/10.1093/ajh/hpad114
  4. Jansen van Vuren, E., Malan, L., Cockeran, M., Scheepers, J. D., Oosthuizen, W., Malan, N. T. (2016). Fibrosis and coronary perfusion – a cardiovascular disease risk in an African male cohort: The SABPA study. Clinical and Experimental Hypertension, 38 (5), 482–488. https://doi.org/10.3109/10641963.2016.1151524
  5. Ekström, M., Hellman, A., Hasselström, J., Hage, C., Kahan, T., Ugander, M. et al. (2020). The Transition from Hypertension to Hypertensive Heart Disease and Heart Failure: The Prefers Hypertension Study. ESC Heart Failure, 7 (2), 737–746. https://doi.org/10.1002/ehf2.12612
  6. Díez, J., Butler, J. (2023). Growing Heart Failure Burden of Hypertensive Heart Disease: A Call to Action. Hypertension, 80 (1), 13–21. https://doi.org/10.1161/hypertensionaha.122.19373
  7. Nwabuo, C. C., Vasan, R. S. (2020). Pathophysiology of Hypertensive Heart Disease: Beyond Left Ventricular Hypertrophy. Current Hypertension Reports, 22 (2). https://doi.org/10.1007/s11906-020-1017-9
  8. Shenasa, M., Shenasa, H. (2017). Hypertension, left ventricular hypertrophy, and sudden cardiac death. International Journal of Cardiology, 237, 60–63. https://doi.org/10.1016/j.ijcard.2017.03.002
  9. Hamo, C. E., DeJong, C., Hartshorne-Evans, N., Lund, L. H., Shah, S. J., Solomon, S., Lam, C. S. P. (2024). Heart failure with preserved ejection fraction. Nature Reviews Disease Primers, 10 (1). https://doi.org/10.1038/s41572-024-00540-y
  10. Moreno, M. U., Eiros, R., Gavira, J. J., Gallego, C., González, A., Ravassa, S. et al. (2017). The Hypertensive Myocardium. Medical Clinics of North America, 101 (1), 43–52. https://doi.org/10.1016/j.mcna.2016.08.002
  11. Seravalle, G., Mancia, G., Grassi, G. (2014). Role of the Sympathetic Nervous System in Hypertension and Hypertension-Related Cardiovascular Disease. High Blood Pressure & Cardiovascular Prevention, 21 (2), 89–105. https://doi.org/10.1007/s40292-014-0056-1
  12. te Riet, L., van Esch, J. H. M., Roks, A. J. M., van den Meiracker, A. H., Danser, A. H. J. (2015). Hypertension. Circulation Research, 116 (6), 960–975. https://doi.org/10.1161/circresaha.116.303587
  13. Guzik, T. J., Nosalski, R., Maffia, P., Drummond, G. R. (2024). Immune and inflammatory mechanisms in hypertension. Nature Reviews Cardiology, 21 (6), 396–416. https://doi.org/10.1038/s41569-023-00964-1
  14. Zhang, Z., Zhao, L., Zhou, X., Meng, X., Zhou, X. (2023). Role of inflammation, immunity, and oxidative stress in hypertension: New insights and potential therapeutic targets. Frontiers in Immunology, 13. https://doi.org/10.3389/fimmu.2022.1098725
  15. Drummond, G. R., Vinh, A., Guzik, T. J., Sobey, C. G. (2019). Immune mechanisms of hypertension. Nature Reviews Immunology, 19 (8), 517–532. https://doi.org/10.1038/s41577-019-0160-5
  16. Wang, L., Cheng, C. K., Yi, M., Lui, K. O., Huang, Y. (2022). Targeting endothelial dysfunction and inflammation. Journal of Molecular and Cellular Cardiology, 168, 58–67. https://doi.org/10.1016/j.yjmcc.2022.04.011
  17. Della Corte, V., Tuttolomondo, A., Pecoraro, R., Di Raimondo, D., Vassallo, V., Pinto, A. (2016). Inflammation, Endothelial Dysfunction and Arterial Stiffness as Therapeutic Targets in Cardiovascular Medicine. Current Pharmaceutical Design, 22 (30), 4658–4668. https://doi.org/10.2174/1381612822666160510124801
  18. Millar, S. R., Harrington, J. M., Perry, I. J., Phillips, C. M. (2021). Associations between a protective lifestyle behaviour score and biomarkers of chronic low-grade inflammation: a cross-sectional analysis in middle-to-older aged adults. International Journal of Obesity, 46 (3), 476–485. https://doi.org/10.1038/s41366-021-01012-z
  19. Li, X., Guo, X., Chang, Y., Zhang, N., Sun, Y. (2022). Analysis of alterations of serum inflammatory cytokines and fibrosis makers in patients with essential hypertension and left ventricular hypertrophy and the risk factors. American Journal of Translational Research, 14 (6), 4097–4103. Available at: https://pmc.ncbi.nlm.nih.gov/articles/PMC9274558/
  20. Zhu, L., Li, C., Liu, Q., Xu, W., Zhou, X. (2019). Molecular biomarkers in cardiac hypertrophy. Journal of Cellular and Molecular Medicine, 23 (3), 1671–1677. https://doi.org/10.1111/jcmm.14129
  21. Tang, Y., Shen, L., Bao, J.-h., Xu, D.-Y. (2023). Deficiency of Tregs in hypertension‐associated left ventricular hypertrophy. The Journal of Clinical Hypertension, 25 (6), 562–572. https://doi.org/10.1111/jch.14660
  22. Dziedzic-Jankowska, K., Pietrzak, R., Szyszka, M., Bujanowicz, A., Stelmaszczyk-Emmel, A., Werner, B., Skrzypczyk, P. (2025). Monocyte-to-Neutrophil Ratio as an Immunological Marker of Left Ventricular Hypertrophy in Children with Primary Hypertension. Journal of Clinical Medicine, 14 (11), 3896. https://doi.org/10.3390/jcm14113896
  23. Kain, D., Amit, U., Yagil, C., Landa, N., Naftali-Shani, N., Molotski, N. et al. (2016). Macrophages dictate the progression and manifestation of hypertensive heart disease. International Journal of Cardiology, 203, 381–395. https://doi.org/10.1016/j.ijcard.2015.10.126
  24. Schiffrin, E. L. (2013). Immune mechanisms in hypertension and vascular injury. Clinical Science, 126 (4), 267–274. https://doi.org/10.1042/cs20130407
  25. Gupta, J., Dominic, E. A., Fink, J. C., Ojo, A. O., Barrows, I. R., Reilly, M. P. et al. (2015). Association between Inflammation and Cardiac Geometry in Chronic Kidney Disease: Findings from the CRIC Study. Plos One, 10 (4), e0124772. https://doi.org/10.1371/journal.pone.0124772
  26. Adewuya, O. A., Ajayi, E. A., Adebayo, A. R., Ojo, O. E., Olaoye, O. B. (2020). Serum uric acid and left ventricular hypertrophy in hypertensive patients in Ado-Ekiti. Pan African Medical Journal, 36. https://doi.org/10.11604/pamj.2020.36.190.21072
  27. Uchinaka, A., Yoneda, M., Yamada, Y., Murohara, T., Nagata, K. (2017). Effects of mTOR inhibition on cardiac and adipose tissue pathology and glucose metabolism in rats with metabolic syndrome. Pharmacology Research & Perspectives, 5 (4). https://doi.org/10.1002/prp2.331
  28. Sriramula, S., Francis, J. (2015). Tumor Necrosis Factor – Alpha Is Essential for Angiotensin II-Induced Ventricular Remodeling: Role for Oxidative Stress. Plos One, 10 (9), e0138372. https://doi.org/10.1371/journal.pone.0138372
  29. Boarescu, P.-M., Boarescu, I., Pop, R. M., Roşian, Ş. H., Bocșan, I. C., Rus, V. et al. (2022). Evaluation of Oxidative Stress Biomarkers, Pro-Inflammatory Cytokines, and Histological Changes in Experimental Hypertension, Dyslipidemia, and Type 1 Diabetes Mellitus. International Journal of Molecular Sciences, 23 (3), 1438. https://doi.org/10.3390/ijms23031438
  30. Barbaro, N. R., Fontana, V., Sabbatini, A. R., Ritter, A. M., Faria, A. P., Correa, N. B. et al. (2015). Relationship of extracellular matrix biomarkers with left ventricular hypertrophy in resistant hypertension. Journal of the American Society of Hypertension, 9 (4), e2–e3. https://doi.org/10.1016/j.jash.2015.03.014
  31. Ribeiro Vitorino, T., Ferraz do Prado, A., Bruno de Assis Cau, S., Rizzi, E. (2023). MMP-2 and its implications on cardiac function and structure: Interplay with inflammation in hypertension. Biochemical Pharmacology, 215, 115684. https://doi.org/10.1016/j.bcp.2023.115684
  32. M. Ciulla, M., Paliotti, R., Carini, M., Magrini, F., Aldini, G. (2011). Fibrosis, Enzymatic and Non-Enzymatic Cross-Links in Hypertensive Heart Disease. Cardiovascular & Hematological Disorders-Drug Targets, 11 (2), 61–73. https://doi.org/10.2174/187152911798347025
  33. Sell, D. R., Monnier, V. M. (2012). Molecular Basis of Arterial Stiffening: Role of Glycation – A Mini-Review. Gerontology, 58 (3), 227–237. https://doi.org/10.1159/000334668
  34. Song, W., Zhang, C., Tang, J., Li, Y., Jiao, T., Lin, X. et al. (2023). Hypersensitive C-reactive protein as a potential indicator for predicting left ventricular hypertrophy in elderly community-dwelling patients with hypertension. BMC Cardiovascular Disorders, 23 (1). https://doi.org/10.1186/s12872-023-03509-z
  35. Koval, S. M., Mysnichenko, O. V., Penkova, M. Y. (2020). A highly sensitive C-reactive protein and its relationship with features of arterial hypertension in patients with abdominal obesity. Problems of Endocrine Pathology, 74 (4), 60–65. https://doi.org/10.21856/j-PEP.2020.4.07
  36. Koval, S., Snigurska, I., Bozhko, V., Miloslavsky, D. (2021). The problem of hypertensive heart disease regression in patients with arterial hypertension. Hypertension, 13 (6), 28–34. https://doi.org/10.22141/2224-1485.13.6.2020.223078
  37. Cortez, A. F., Muxfeldt, E. S., Cardoso, C. R. L., Salles, G. F. (2016). Prognostic Value of C-Reactive Protein in Resistant Hypertension. American Journal of Hypertension, 29 (8), 992–1000. https://doi.org/10.1093/ajh/hpw011
  38. Zlibut, A., Bocsan, I. C., Agoston-Coldea, L. (2019). Pentraxin-3 and endothelial dysfunction. Advances in Clinical Chemistry. Elsevier, 163–179. https://doi.org/10.1016/bs.acc.2019.03.005
  39. Mkhize, S. A., Manilall, A., Mokotedi, L., Gunter, S., Michel, F. S. (2024). Involvement of pentraxin‐3 in the development of hypertension but not left ventricular hypertrophy in male spontaneously hypertensive rats. Physiological Reports, 12 (20). https://doi.org/10.14814/phy2.70086
  40. Mocan, M., Mocan Hognogi, L. D., Anton, F. P., Chiorescu, R. M., Goidescu, C. M., Stoia, M. A., Farcas, A. D. (2019). Biomarkers of Inflammation in Left Ventricular Diastolic Dysfunction. Disease Markers, 2019, 1–14. https://doi.org/10.1155/2019/7583690
  41. Smykiewicz, P., Segiet, A., Keag, M., Żera, T. (2018). Proinflammatory cytokines and ageing of the cardiovascular-renal system. Mechanisms of Ageing and Development, 175, 35–45. https://doi.org/10.1016/j.mad.2018.07.006
  42. Wen, Y., Crowley, S. D. (2019). Renal Effects of Cytokines in Hypertension. Renal Fibrosis: Mechanisms and Therapies. Singapore: Springer, 443–454. https://doi.org/10.1007/978-981-13-8871-2_21
  43. Tanase, D. M., Gosav, E. M., Radu, S., Ouatu, A., Rezus, C., Ciocoiu, M. et al. (2019). Arterial Hypertension and Interleukins: Potential Therapeutic Target or Future Diagnostic Marker? International Journal of Hypertension, 2019, 1–17. https://doi.org/10.1155/2019/3159283
  44. Bonaventura, A., Moroni, F., Golino, M., Del Buono, M. G., Vecchié, A., Potere, N., Abbate, A. (2024). IL-1 blockade in cardiovascular disease: an appraisal of the evidence across different inflammatory paradigms. Minerva Cardiology and Angiology, 72 (5), 477–488. https://doi.org/10.23736/s2724-5683.23.06390-1
  45. Zan, Y., Wang, J., Wang, W., Cui, T., Xu, K., Li, Y. (2022). Inflammatory cytokines and their correlations with different left ventricular geometries and functions in PHT patients. Echocardiography, 39 (12), 1589–1600. https://doi.org/10.1111/echo.15495
  46. Chou, C.-H., Hung, C.-S., Liao, C.-W., Wei, L.-H., Chen, C.-W., Shun, C.-T. et al. (2018). IL-6 trans-signalling contributes to aldosterone-induced cardiac fibrosis. Cardiovascular Research, 114 (5), 690–702. https://doi.org/10.1093/cvr/cvy013
  47. Hasanah, U., Rejeki, P. S., Wungu, C. D. K., Pranoto, A., Izzatunnisa, N., Rahmanto, I., Halim, S. (2024). High-intensity combination exercise has the highest effect on increasing serum irisin and interleukin 6 levels in women with obesity. Journal of Basic and Clinical Physiology and Pharmacology, 35 (1-2), 71–78. https://doi.org/10.1515/jbcpp-2023-0150
  48. Stawski, L., Trojanowska, M. (2018). Oncostatin M and its role in fibrosis. Connective Tissue Research, 60 (1), 40–49. https://doi.org/10.1080/03008207.2018.1500558
  49. Jengelley, D. H. A., Wang, M., Narasimhan, A., Rupert, J. E., Young, A. R., Zhong, X. et al. (2022). Exogenous Oncostatin M induces Cardiac Dysfunction, Musculoskeletal Atrophy, and Fibrosis. Cytokine, 159, 155972. https://doi.org/10.1016/j.cyto.2022.155972
  50. González, A., López, B., Ravassa, S., Beaumont, J., Zudaire, A., Gallego, I. et al. (2012). Cardiotrophin-1 in hypertensive heart disease. Endocrine, 42 (1), 9–17. https://doi.org/10.1007/s12020-012-9649-4
  51. Ravassa, S., Beloqui, O., Varo, N., Barba, J., López, B., Beaumont, J. et al. (2013). Association of cardiotrophin-1 with left ventricular systolic properties in asymptomatic hypertensive patients. Journal of Hypertension, 31 (3), 587–594. https://doi.org/10.1097/hjh.0b013e32835ca903
  52. Hou, X., Hu, Z., Huang, X., Chen, Y., He, X., Xu, H., Wang, N. (2013). Serum osteopontin, but not OPN gene polymorphism, is associated with LVH in essential hypertensive patients. Journal of Molecular Medicine, 92 (5), 487–495. https://doi.org/10.1007/s00109-013-1099-9
  53. Zhuang, T., Chen, M.-H., Wu, R.-X., Wang, J., Hu, X.-D., Meng, T. et al. (2024). ALKBH5-mediated m6A modification of IL-11 drives macrophage-to-myofibroblast transition and pathological cardiac fibrosis in mice. Nature Communications, 15 (1). https://doi.org/10.1038/s41467-024-46357-x
  54. Bhattarai, U., He, X., Xu, R., Liu, X., Pan, L., Sun, Y. et al. (2023). IL-12α deficiency attenuates pressure overload-induced cardiac inflammation, hypertrophy, dysfunction, and heart failure progression. Frontiers in Immunology, 14. https://doi.org/10.3389/fimmu.2023.1105664
  55. Huang, L. (2024). The role of IL-17 family cytokines in cardiac fibrosis. Frontiers in Cardiovascular Medicine, 11. https://doi.org/10.3389/fcvm.2024.1470362
  56. ÖZzbïçer, S., Uluçam, Z. M. (2017). Association Between Interleukin-18 Level and Left Ventricular Mass Index in Hypertensive Patients. Korean Circulation Journal, 47 (2), 238. https://doi.org/10.4070/kcj.2016.0351
  57. Jiang, C., Jin, X., Li, C., Wen, L., Wang, Y., Li, X. et al. (2023). Roles of IL-33 in the Pathogenesis of Cardiac Disorders. Experimental Biology and Medicine, 248, 2167–2174. https://doi.org/10.1177/15353702231198075
  58. Wang, X., Han, S.-J., Wang, X.-L., Xu, Y.-F., Wang, H.-C., Peng, J.-Y. et al. (2024). Soluble ST2 Is a Biomarker Associated With Left Ventricular Hypertrophy and Concentric Hypertrophy in Patients With Essential Hypertension. American Journal of Hypertension, 37 (12), 987–994. https://doi.org/10.1093/ajh/hpae105
  59. Therrien, F. J., Agharazii, M., Lebel, M., Larivière, R. (2012). Neutralization of Tumor Necrosis Factor-Alpha Reduces Renal Fibrosis and Hypertension in Rats with Renal Failure. American Journal of Nephrology, 36 (2), 151–161. https://doi.org/10.1159/000340033
  60. Kumar, V., Bansal, S. S. (2025). Immunological Regulation of Fibrosis During Heart Failure: It Takes Two to Tango. Biomolecules, 15 (1), 58. https://doi.org/10.3390/biom15010058
  61. Wang, X., Han, W., Han, L., Yang, J., Li, K., Fan, Y. (2021). Levels of Serum sST2, MMP-3, and Gal-3 in Patients with Essential Hypertension and Their Correlation with Left Ventricular Hypertrophy. Evidence-Based Complementary and Alternative Medicine, 2021, 1–6. https://doi.org/10.1155/2021/7262776
  62. Rothman, A. M., MacFadyen, J., Thuren, T., Webb, A., Harrison, D. G., Guzik, T. J. et al. (2020). Effects of Interleukin-1β Inhibition on Blood Pressure, Incident Hypertension, and Residual Inflammatory Risk. Hypertension, 75 (2), 477–482. https://doi.org/10.1161/hypertensionaha.119.13642
  63. Krishnan, S. M., Sobey, C. G., Latz, E., Mansell, A., Drummond, G. R. (2014). IL‐1β and IL‐18: inflammatory markers or mediators of hypertension? British Journal of Pharmacology, 171 (24), 5589–5602. https://doi.org/10.1111/bph.12876
  64. Matsushita, N., Ishida, N., Ibi, M., Saito, M., Takahashi, M., Taniguchi, S. et al. (2019). IL-1β Plays an Important Role in Pressure Overload-Induced Atrial Fibrillation in Mice. Biological and Pharmaceutical Bulletin, 42 (4), 543–546. https://doi.org/10.1248/bpb.b18-00363
  65. Tsioufis, C., Konstantinidis, D., Nikolakopoulos, I., Vemmou, E., Kalos, T., Georgiopoulos, G. et al. (2019). Biomarkers of Atrial Fibrillation in Hypertension. Current Medicinal Chemistry, 26 (5), 888–897. https://doi.org/10.2174/0929867324666171006155516
  66. Wang, H., Hou, L., Kwak, D., Fassett, J., Xu, X., Chen, A. et al. (2016). Increasing Regulatory T Cells With Interleukin-2 and Interleukin-2 Antibody Complexes Attenuates Lung Inflammation and Heart Failure Progression. Hypertension, 68 (1), 114–122. https://doi.org/10.1161/hypertensionaha.116.07084
  67. Wenzel, U. O., Bode, M., Kurts, C., Ehmke, H. (2018). Salt, inflammation, IL‐17 and hypertension. British Journal of Pharmacology, 176 (12), 1853–1863. https://doi.org/10.1111/bph.14359
  68. Higaki, A., Mahmoud, A. U. M., Paradis, P., Schiffrin, E. L. (2020). Role of interleukin-23/interleukin-17 axis in T-cell-mediated actions in hypertension. Cardiovascular Research, 117 (5), 1274–1283. https://doi.org/10.1093/cvr/cvaa257
  69. Xiang, L., Yin, G., Gong, Z., Lv, X., Feng, C., Liu, L. et al. (2025). IL-22 Attenuates Pressure Overload-Induced Heart Failure and Inflammation. Journal of Cardiovascular Translational Research, 18 (3), 471–483. https://doi.org/10.1007/s12265-025-10613-2
  70. Frangogiannis, N. G. (2020). Transforming growth factor–β in tissue fibrosis. Journal of Experimental Medicine, 217 (3). https://doi.org/10.1084/jem.20190103
  71. Zhao, M., Zheng, S., Yang, J., Wu, Y., Ren, Y., Kong, X. et al. (2015). Suppression of TGF-β1/Smad Signaling Pathway by Sesamin Contributes to the Attenuation of Myocardial Fibrosis in Spontaneously Hypertensive Rats. Plos One, 10 (3), e0121312. https://doi.org/10.1371/journal.pone.0121312
  72. Frohlich, J., Vinciguerra, M. (2020). Candidate rejuvenating factor GDF11 and tissue fibrosis: friend or foe? GeroScience, 42 (6), 1475–1498. https://doi.org/10.1007/s11357-020-00279-w
  73. Machelak, W., Szczepaniak, A., Jacenik, D., Zielińska, M. (2023). The role of GDF11 during inflammation – An overview. Life Sciences, 322, 121650. https://doi.org/10.1016/j.lfs.2023.121650
  74. Koval, S., Miloslavsky, D., Snihurskaya, I., Bozhko, V., Penkova, M., Shchenyavskaya, E. (2018). Growth differentiation factor 11: general biological properties, metabolic effects and possible pathophysiological role in arterial hypertension, obesity, diabetes mellitus and age-dependent pathology (literature review). International Journal of Endocrinology (Ukraine), 14 (6), 621–635. https://doi.org/10.22141/2224-0721.14.6.2018.146077
  75. Kou, H., Jin, X., Gao, D., Ma, R., Dong, X., Wei, J., Wang, X. (2017). Association between growth differentiation factor 15 and left ventricular hypertrophy in hypertensive patients and healthy adults. Clinical and Experimental Hypertension, 40 (1), 8–15. https://doi.org/10.1080/10641963.2016.1273948
  76. Rudemiller, N. P., Crowley, S. D. (2017). The role of chemokines in hypertension and consequent target organ damage. Pharmacological Research, 119, 404–411. https://doi.org/10.1016/j.phrs.2017.02.026
  77. Bettink, S. I., Werner, C., Chen, C.-H., Müller, P., Schirmer, S. H., Walenta, K. L. et al. (2010). Integrin-linked kinase is a central mediator in angiotensin II type 1- and chemokine receptor CXCR4 signaling in myocardial hypertrophy. Biochemical and Biophysical Research Communications, 397 (2), 208–213. https://doi.org/10.1016/j.bbrc.2010.05.086
  78. Hogas, S., Bilha, S. C., Branisteanu, D., Hogas, M., Gaipov, A., Kanbay, M., Covic, A. (2017). Potential novel biomarkers of cardiovascular dysfunction and disease: cardiotrophin-1, adipokines and galectin-3. Archives of Medical Science, 4, 897–913. https://doi.org/10.5114/aoms.2016.58664
  79. Peer, M., Mashavi, M., Matas, Z., Harpaz, D., Shargorodsky, M. (2014). Adiponectin as an Independent Predictor of Left Ventricular Hypertrophy in Nondiabetic Patients With Hypertension. Angiology, 66 (3), 219–224. https://doi.org/10.1177/0003319714523332
  80. Chen, K., Zhou, M., Wang, X., Li, S., Yang, D. (2019). The Role of Myokines and Adipokines in Hypertension and Hypertension-related Complications. Hypertension Research, 42 (10), 1544–1551. https://doi.org/10.1038/s41440-019-0266-y
  81. Ho, M.-Y., Wang, C.-Y. (2021). Role of Irisin in Myocardial Infarction, Heart Failure, and Cardiac Hypertrophy. Cells, 10 (8), 2103. https://doi.org/10.3390/cells10082103
  82. Palao, T., Medzikovic, L., Rippe, C., Wanga, S., Al-Mardini, C., van Weert, A. et al. (2018). Thrombospondin-4 mediates cardiovascular remodelling in angiotensin II-induced hypertension. Cardiovascular Pathology, 35, 12–19. https://doi.org/10.1016/j.carpath.2018.03.003
  83. Cao, M., Yuan, W., Peng, M., Mao, Z., Zhao, Q., Sun, X., Yan, J. (2019). Role of CyPA in cardiac hypertrophy and remodeling. Bioscience Reports, 39 (12). https://doi.org/10.1042/bsr20193190
  84. Duman, H., Bahçeci, I., Çinier, G., Duman, H., Bakırcı, E. M., Çetin, M. (2018). Left ventricular hypertrophy is associated with increased sirtuin level in newly diagnosed hypertensive patients. Clinical and Experimental Hypertension, 41 (6), 511–515. https://doi.org/10.1080/10641963.2018.1510946
  85. Ritter, A. M. V., Faria, A. P. C. d., Sabbatini, A., Corrêa, N. B., Brunelli, V., Modolo, R., Moreno, H. (2017). MCP-1 Levels are Associated with Cardiac Remodeling but not with Resistant Hypertension. Arquivos Brasileiros de Cardiologia, 108 (4). https://doi.org/10.5935/abc.20170033
  86. Chi, H., Feng, H., Shang, X., Jiao, J., Sun, L., Jiang, W. et al. (2019). Circulating Connective Tissue Growth Factor Is Associated with Diastolic Dysfunction in Patients with Diastolic Heart Failure. Cardiology, 143 (3-4), 77–84. https://doi.org/10.1159/000499179
  87. Zhou, X., Jeong, E.-M., Liu, H., Kaseer, B., Liu, M., Shrestha, S. et al. (2022). Circulating S‐Glutathionylated cMyBP‐C as a Biomarker for Cardiac Diastolic Dysfunction. Journal of the American Heart Association, 11 (11). https://doi.org/10.1161/jaha.122.025295
  88. Xu, X., Hua, Y., Nair, S., Bucala, R., Ren, J. (2014). Macrophage Migration Inhibitory Factor Deletion Exacerbates Pressure Overload–Induced Cardiac Hypertrophy Through Mitigating Autophagy. Hypertension, 63 (3), 490–499. https://doi.org/10.1161/hypertensionaha.113.02219
  89. Zhang, J., Yang, L., Ding, Y. (2021). Effects of irbesartan on phenotypic alterations in monocytes and the inflammatory status of hypertensive patients with left ventricular hypertrophy. BMC Cardiovascular Disorders, 21 (1). https://doi.org/10.1186/s12872-021-02004-7
  90. Lin, M., Heizati, M., Wang, L., Nurula, M., Yang, Z., Wang, Z. et al. (2021). A systematic review and meta-analysis of effects of spironolactone on blood pressure, glucose, lipids, renal function, fibrosis and inflammation in patients with hypertension and diabetes. Blood Pressure, 30 (3), 145–153. https://doi.org/10.1080/08037051.2021.1880881
  91. Fang, T., Guo, B., Xue, L., Wang, L. (2019). Atorvastatin Prevents Myocardial Fibrosis in Spontaneous Hypertension via Interleukin-6 (IL-6)/Signal Transducer and Activator of Transcription 3 (STAT3)/Endothelin-1 (ET-1) Pathway. Medical Science Monitor, 25, 318–323. https://doi.org/10.12659/msm.912032
  92. Kim, H.-L., Lee, J. P., An, J. N., Kim, J. H., Lim, W.-H., Seo, J.-B. et al. (2016). Soluble Tumor Necrosis Factor Receptors and Arterial Stiffness in Patients With Coronary Atherosclerosis. American Journal of Hypertension, 30 (3), 313–318. https://doi.org/10.1093/ajh/hpw134
  93. Duerrschmid, C., Crawford, J. R., Reineke, E., Taffet, G. E., Trial, J., Entman, M. L., Haudek, S. B. (2013). TNF receptor 1 signaling is critically involved in mediating angiotensin-II-induced cardiac fibrosis. Journal of Molecular and Cellular Cardiology, 57, 59–67. https://doi.org/10.1016/j.yjmcc.2013.01.006
Proinflammatory humoral factors and their role in the pathogenesis of left ventricular hypertrophy in hypertension (literature review)

Downloads

Published

2026-05-29

How to Cite

Myloslavskyi, D., Koval, S., Mysnychenko, O., Lytvynova, O., & Shcheniavska, O. (2026). Proinflammatory humoral factors and their role in the pathogenesis of left ventricular hypertrophy in hypertension (literature review). ScienceRise: Medical Science, (1 (66), 10–19. https://doi.org/10.15587/2519-4798.2026.361623

Issue

Section

Medical Science