Characteristics of the psoas minor muscle in modeling lateral interbody spondylodesis of the lumbar spine

Cover Page

Cite item

Full Text

Abstract

ВACKGROUND: For the treatment of degenerative diseases of the spine, various deformities, a minimally invasive technique of lateral lumbar interbody fusion is used, which minimizes the risks of spinal cord injury. In the development of these pathologies, the most important role is assigned to the paraspinal muscles, the histological features of which are insufficiently elucidated in the relevant literature when modeling spondylodesis.

АIM: To investigate the effect of lateral interbody vertebral fusion (spondylodesis) when introducing titanium implants on the histostructure of the psoas minor muscle.

МATERIALS AND METHODS: Experiments were performed in 14 mongrel dogs, 3 individuals — the control group (norm). The аnimals underwent discectomy at the level of L4–5, L5–6 vertebrae through the lateral approach on the right, and interbody titanium implants were installed. The lumbar spine was stabilized with an external fixator for 30 days. Paraffin muscle sections were stained with hematoxylin-eosin, according to Masson.

RESULTS: During the experiment, an increased variety of myosymplast diameters, loss of polygonality of their profiles, fibrosis of the interstitial space, and sclerotization of the vascular membranes were observed in the psoas minor muscle. The volume density of endomysium in both muscles increased 1.5 times relative to the norm after 6 months Other parameters decreased: the volume of myosymplasts was 95%, that of microvessels — 73% on the left, 83% on the right. On the other hand, the degree of fatty infiltration increased, amounting to 276% on the left and 394% — on the right of the normal parameters. After 18 months, the bulk density of muscle fibers on the left was restored to the value in the control, on the right it was only 95%. The degree of sclerotization in the muscle on the left is 133%, on the right — 161% of the norm; the index of fatty infiltration was 146% on the left and 339% on the right of the normal parameter.

CONCLUSION: pathohistological changes in the psoas minor during lateral interbody fusion are more pronounced on the side of the operative approach, which necessitates minimizing trauma to the paravertebral muscles during operations in order to prevent sclerotization and fatty involution of muscle tissue.

About the authors

Galina N. Filimonova

Russian Ilisarov Medical Research Center for Traumatology and Orthopedics

Author for correspondence.
Email: galnik.kurgan@yandex.ru
ORCID iD: 0000-0002-8929-8784
SPIN-code: 3007-1309
Scopus Author ID: 57196004532

Cand. Sci. (Biol.), senior researcher

Russian Federation, Kurgan

Olga V. Diuriagina

Russian Ilisarov Medical Research Center for Traumatology and Orthopedics

Email: diuriagina@mail.ru
ORCID iD: 0000-0001-9974-2204
SPIN-code: 8301-1475

Cand. Sci. (Vet.), head of the experimental laboratory

Russian Federation, Kurgan

Nikolai I. Antonov

Russian Ilisarov Medical Research Center for Traumatology and Orthopedics

Email: aniv-niko@mail.ru
ORCID iD: 0000-0002-8627-2749
SPIN-code: 3754-7508
Scopus Author ID: 55207639900

Cand. Sci. (Biol.), researcher

Russian Federation, Kurgan

Sergei O. Ryabykh

N.N. Priorov Russian Scientific Research Institute of Traumatology and Orthopedics

Email: ryabykhco@cito-priorov.ru
ORCID iD: 0000-0002-8293-0521
SPIN-code: 6382-1107
Scopus Author ID: 54941390600

MD, Dr. Sci. (Med.), traumatologist-ortopedist, pediatric and spinal surgeon

Russian Federation, Moscow

References

  1. Liang C, Sun J, Cui X, et al. Spinal sagittal imbalance in patients with lumbar disc herniation: its spinopelvic characteristics, strength changes of the spinal musculature and natural history after lumbar discectomy. BMC Musculoskelet Disord. 2016;17:305. doi: 10.1186/s12891-016-1164-y
  2. Jun HS, Kim JH, Ahn JH, et al. The effect of lumbar spinal muscle on spinal sagittal alignment: evaluating muscle quantity and quality. Neurosurgery. 2016;79(6):847–855. doi: 10.1227/NEU.0000000000001269
  3. Hori Y, Hoshino M, Inage K, et al. Clinical importance of trunk muscle mass for low back pain, spinal balance, and quality of life– a multicenter cross-sectional study. Eur Spine J. 2019;28(5):914–921. doi: 10.1007/s00586-019-05904-7
  4. Hiyama A, Katoh H, Sakai D, et al. The correlation analysis between sagittal alignment and cross-sectional area of paraspinal muscle in patients with lumbar spinal stenosis and degenerative spondylolisthesis. BMC Musculoskelet Disord. 2019;20(1):352. doi: 10.1186/s12891-019-2733-7
  5. He K, Head J, Mouchtouris N, et al. The implications of paraspinal muscle atrophy in low back pain, thoracolumbar pathology, and clinical outcomes after spine surgery: a review of the literature. Global Spine J. 2020;10(5):657–666. doi: 10.1177/2192568219879087
  6. Shchurova EN, Filimonova GN, Ryabykh SO. Magnitude of thoracic spine deformity affecting morphological characteristics of paraspinal muscles in patients with severe idiopathic scoliosis. Genij ortopedii. 2021;27(1):68–73. (In Russ). doi: 10.18019/1028-4427-2021-27-1-68-73
  7. Shahidi B, Fisch KM, Gibbons MC, Ward SR. Increased fibrogenic gene expression in multifidus muscles of patients with chronic versus acute lumbar spine pathology. Spine (Phila Pa 1976). 2020;45(4):E189–E195. doi: 10.1097/BRS.0000000000003243
  8. Xia W, Fu H, Zhu Z, et al. Association between back muscle degeneration and spinal-pelvic parameters in patients with degenerative spinal kyphosis. BMC Musculoskelet Disord. 2019;20(1):454. doi: 10.1186/s12891-019-2837-0
  9. Park MS, Moon SH, Kim TH, et al. Paraspinal muscles of patients with lumbar diseases. J Neurol Surg A Cent Eur Neurosurg. 2018;79(4):323–329. doi: 10.1055/s-0038-1639332
  10. Lee JC, Cha JG, Kim Y, et al. Quantitative analysis of back muscle degeneration in the patients with the degenerative lumbar flat back using a digital image analysis: comparison with the normal controls. Spine (Phila Pa 1976). 2008;33(3):318–325. doi: 10.1097/BRS.0b013e318162458f
  11. Storheim K, Berg L, Hellum C, et al. Fat in the lumbar multifidus muscles - predictive value and change following disc prosthesis surgery and multidisciplinary rehabilitation in patients with chronic low back pain and degenerative disc: 2-year follow-up of a randomized trial. BMC Musculoskelet Disord. 2017;18(1):145. doi: 10.1186/s12891-017-1505-5
  12. Baykov ES, Verner NYu. Key points of interbody fusion following surgical decompression and stabilization of the lumbosacral spine: literature review. Genij ortopedii. 2020;26(3):426–431. (In Russ). doi: 10.18019/1028-4427-2020-26-3-426-431
  13. Klimov VS, Vasilenko II, Evsyukov AV, et al. The use of LLIF technology in adult patients with degenerative scoliosis: retrospective cohort analysis and literature review. Genij ortopedii. 2018;24(3):393–403. (In Russ). doi: 10.18019/1028-4427-2018-24-3-393-403
  14. Taba HA, Williams SK. Lateral lumbar interbody fusion. Neurosurg Clin N Am. 2020;31(1):33–42. doi: 10.1016/j.nec.2019.08.004
  15. Shihata S. Indirect decompression of the neural elements utilizing direct lateral interbody fusion procedure. Med Arch. 2020;74(2):126–130. doi: 10.5455/medarh.2020.74.126-130
  16. Shimizu T, Fujibayashi S, Otsuki B, et al. Indirect decompression with lateral interbody fusion for severe degenerative lumbar spinal stenosis: minimum 1-year MRI follow-up. J Neurosurg Spine. 2020;1–8. doi: 10.3171/2020.1.SPINE191412
  17. Pourtaheri S, Issa K, Lord E, et al. Paraspinal muscle atrophy after lumbar spine surgery. Orthopedics. 2016;39(2):e209–e214. doi: 10.3928/01477447-20160129-07
  18. Kirsanov KP, Timofeev VN, Menshchikova IA. Methods and technical means for external fixation of the lumbar spine. Veterinariia. 2001;(8):36–40. (In Russ).
  19. Gaidyshev IP. Modelirovanie stokhasticheskikh i determinirovannykh sistem. Rukovodstvo pol’zovatelya programmy AtteStat. Kurgan; 2015. 484 p. (In Russ).
  20. Scott HW, McKee WM. Laminectomy for 34 dogs with thoracolumbar intervertebral disc disease and loss of deep pain perception. J Small Anim Pract. 1999;40(9):417–422. doi: 10.1111/j.1748-5827.1999.tb03114.x
  21. Sousa-Victor P, Gutarra S, García-Prat L, et al. Geriatric muscle stem cells switch reversible quiescence into senescence. Nature. 2014;506(7488):316–321. doi: 10.1038/nature13013
  22. Bok DH, Kim J, Kim TH. Comparison of MRI-defined back muscles volume between patients with ankylosing spondylitis and control patients with chronic back pain: age and spinopelvic alignment matched study. Eur Spine J. 2017;26(2):528–537. doi: 10.1007/s00586-016-4889-2
  23. Khan AB, Weiss EH, Khan AW, et al. Back muscle morphometry: effects on outcomes of spine surgery. World Neurosurg. 2017;103:174–179. doi: 10.1016/j.wneu.2017.03.097
  24. Russian National Standard (GOST) R 33044-2014 No. 71-P. “Principles of Good Laboratory Practice” dated October 20, 2014. Available from: https://docs.cntd.ru/document/1200115791 (In Russ).
  25. Russian National Standard (GOST) 33215-2014 No. 73-P “Guidelines for the maintenance and care of laboratory animals. Rules for equipping premises and organizing procedures” dated December 22, 2014. Available from: https://docs.cntd.ru/document/1200127789 (In Russ).
  26. Russian National Standard (GOST) 33217-2014 No. 73-P “Guidelines for the maintenance and care of laboratory animals. Rules for the maintenance and care of laboratory predatory mammals” dated December 22, 2014. Available from: https://docs.cntd.ru/document/1200127290 (In Russ).
  27. Sanitary Rules 2.2.1.3218-14 No. 34547 “Sanitary and epidemiological requirements for the arrangement, equipment and maintenance of experimental biological clinics (vivariums)” dated October 31, 2014. Available from: https://docs.cntd.ru/document/420219460 (In Russ).

Supplementary files

Supplementary Files
Action
1. JATS XML
2. Fig. 1. Operating field. View of the implant after insertion into the interbody space.

Download (204KB)
3. Fig. 2. The appearance of the ventral surface of the canine lumbar region six months after surgery. Right — m. psoas minor on the right, Left — the muscle on the left; L4–5, L5–6 — level of interbody implant placement.

Download (200KB)
4. Fig. 3. Histostructure of m. psoas minor in control: a — polygonal profiles of fibers, minimum endomysium; b — nerve trunk without pathology. Fragments of paraffin sections, stained with hematoxylin-eosin, magnification: а — ×400; b — ×200.

Download (350KB)
5. Fig. 4. Histostructure of m. psoas minor after six months of the experiment on the left (a) and on the right (b): a — various profiles and diameters of myosymplasts; b — a vessel of the arterial unit link with signs of adventitial fibrosis and thickened t. media, smooth muscle cells are disoriented. The fragments of paraffin sections, stained with hematoxylin-eosin, magnification — ×400.

Download (352KB)
6. Fig. 5. Histostructure of m. psoas minor after 12 (a, b), 18 (c–e) months of the experiment to the left (a, c) and to the right (b, d, e) of the spine: a, b — polygonal profiles of muscle fibers, normostructure of vessels and neuromuscular spindles, accumulations of adipocytes in the perimysial space; c — fibrosis of the endomysium, single adipocytes in bundles of myosymplasts, in the enlarged perimysium of accumulations of fat cells; d — fragment of muscle tissue fibrosis with myocytes of various profiles; e — spasmodic vessels are immersed in accumulations of adipocytes that have replaced muscle fibers. Fragments of paraffin sections, stained with hematoxylin-eosin, magnification: ×400; c — ×200.

Download (752KB)

Copyright (c) 2022 Eco-Vector



This website uses cookies

You consent to our cookies if you continue to use our website.

About Cookies