Role of Inflammatory Mediators, Growth Factors, and Osteodystrophy in Recurrent Lumbar Disk Herniation
- Authors: Chekhonatskiy V.A.1, Dreval O.N.1, Kuznetsov A.V.1, Chekhonatskiy A.A.2, Zakharova N.B.2, Grishina E.A.1, Gorozhanin A.V.3, Volna V.V.3
-
Affiliations:
- Russian Medical Academy of Continuous Professional Education
- Saratov State Medical University named after V.I. Razumovsky
- S.P. Botkin City Clinical Hospital
- Issue: Vol 17, No 2 (2023)
- Pages: 36-42
- Section: Original articles
- URL: https://journals.rcsi.science/2075-5473/article/view/131727
- DOI: https://doi.org/10.54101/ACEN.2023.2.5
- ID: 131727
Cite item
Full Text
Abstract
Introduction. Reintervention in patients with spinal disk herniation is shown to significantly decrease likelihood of favorable outcomes in the postoperative period. Thus, it is important to individually assess risk factors for and likelihood of spinal disk herniation recurrence for each patient, and choose a suitable surgical option.
Objective: to evaluate changes in the levels of immunoregulatory mediators in the blood serum and extracted spinal disc tissue of allegedly healthy individuals and patients with lumbar disk herniation relapses.
Materials and methods. We examined 60 patients. The control group included 19 patients with traumatic spinal cord injuries at the lumbar level. The main group included 41 patients with spinal disk herniation. Twenty-two individuals had primary herniation while 11 patients presented with single clinical and neurological relapses at the pre-operated lumbar level and 8 patients presented with recurrent relapses. Solid-phase enzyme immunoassay detected proinflammatory cytokines (interleukin-6, tumor necrosis factor-α), chemokines (interleukin-8, monocyte chemoattractant protein-1), growth factors (vascular endothelial growth factor, transforming growth factor-β1), and osteodestruction markers (osteoprogesterin, matrix metalloproteinase-8) in the blood serum and the extracted spinal disc tissue.
Results. We found that spinal disk destruction and chronic inflammation developed with both locally and generally elevating levels of proinflammatory cytokines/chemokines, growth factors, and matrix metalloproteinase 8.
Conclusion. The results emphasize the significance of local changes in the studied parameters to choose and plan personalized surgical treatment in patients with spinal disk herniation.
Full Text
##article.viewOnOriginalSite##About the authors
Vladimir A. Chekhonatskiy
Russian Medical Academy of Continuous Professional Education
Author for correspondence.
Email: fax-1@yandex.ru
ORCID iD: 0000-0001-6155-1154
postgraduate student, Department of neurosurgery
Russian Federation, MoscowOleg N. Dreval
Russian Medical Academy of Continuous Professional Education
Email: odreval@nsi.ru
ORCID iD: 0000-0002-8944-9837
D. Sci. (Med.), Professor, Head, Department of neurosurgery
Russian Federation, MoscowAleksei V. Kuznetsov
Russian Medical Academy of Continuous Professional Education
Email: akuznetsov@nsi.ru
ORCID iD: 0000-0002-9487-6008
Cand. Sci. (Med.), Associate Professor, Department of neurosurgery
Russian Federation, MoscowAndrey A. Chekhonatskiy
Saratov State Medical University named after V.I. Razumovsky
Email: fax-1@yandex.ru
ORCID iD: 0000-0003-3327-1483
D. Sci. (Med.), Head, Department of neurosurgery
Russian Federation, SaratovNatalya B. Zakharova
Saratov State Medical University named after V.I. Razumovsky
Email: lipidgormon@mail.ru
ORCID iD: 0000-0003-0289-3562
D. Sci. (Med.), Professor, Department of clinical laboratory diagnostics
Russian Federation, SaratovElena A. Grishina
Russian Medical Academy of Continuous Professional Education
Email: ncmu@almazovcentre.ru
ORCID iD: 0000-0002-5621-8266
D. Sci. (Med.), Professor, Director, Research Institute of Molecular and Personalized Medicine
Russian Federation, MoscowAleksandr V. Gorozhanin
S.P. Botkin City Clinical Hospital
Email: agorozhanin@list.ru
ORCID iD: 0000-0002-3593-7034
Cand. Sci. (Med.), Head, Neurosurgery department No. 19
Russian Federation, MoscowVera V. Volna
S.P. Botkin City Clinical Hospital
Email: neurosurgeon-sidorenko@mail.ru
neurosurgeon, Neurosurgery department No. 19
Russian Federation, MoscowReferences
- Древаль О.Н., Кузнецов А.В., Чехонацкий В.А. и др. Патогенетические аспекты и факторы риска развития рецидива грыжи диска поясничного отдела позвоночника: обзор литературы. Хирургия позвоночника. 2021;18(1):47–52. Dreval O.N., Kuznetsov A.V., Chekhonatskiy V.A. et al. Pathogenetic aspects and risk factors of lumbar disc herniation recurrence (review of the literature). Journal of Spine Surgery. 2021;18(1):47–52. doi: 10.14531/ss2021.1.47-52
- Чехонацкий В.А., Древаль О.Н., Кузнецов А.В. и др. Современные принципы лечения рецидивов грыж межпозвонкового диска поясничного отдела позвоночника. Саратовский научно-медицинский журнал. 2020;16(3):769–772. Chekhonatskiy V.A., Dreval O.N., Kuznetsov A.V. et al. Modern principles of treatment of recurrent herniation of the intervertebral disc of the lumbar spine. Saratov Journal of Medical Scientific Research. 2020;16(3):769–772.
- Nicholas S., Woojin Cho. Recurrent lumbar disc herniation: a review. Global Spine J. 2019;9(2):202–209. doi: 10.1177/2192568217745063
- Wang J., Markova D., Anderson D.G. et al. TNF-α and IL-1β promote a disintegrin-like and metalloprotease with thrombospondin type I motif-5-mediated aggrecan degradation through syndecan-4 in intervertebral disc. J. Biol. Chem. 2011;286:39738–39749. doi: 10.1074/jbc.M111.264549
- Bachmeier B.E., Nerlich A., Mittermaier N. et al. Matrix metalloproteinase expression levels suggest distinct enzyme roles during lumbar disc herniation and degeneration. Eur. Spine J. 2009;18:1573–1586. doi: 10.1007/s00586-009-1031-8
- Tchetina E.V., Markova G.A. Regulation of energy metabolism in the growth plate and osteoarthritic chondrocytes. Rheumatol. Int. 2018;38(11):1963–1974. doi: 10.1007/s00296-018-4103-4
- Altun I. Cytokine profile in degenerated painful intervertebral disc: variability with respect to duration of symptoms and type of disease. Spine J. 2016;16(7):857–861. doi: 10.1016/j.spinee.2016.03.019
- Bian Q., Ma L., Jain A. et al. Mechanosignaling activation of TGF-P maintains intervertebral disc homeostasis. Bone Res. 2017;5:1–14. doi: 10.1038/boneres.2017.8
- Zheng L., Cao Y., Ni S. et al. Ciliary parathyroid hormone signaling activates transforming growth factor-β to maintain intervertebral disc homeostasis during aging. Bone Res. 2018;6:21. doi: 10.1038/s41413-018-0022-y