# Parametric Finite Element Evaluation of Load Redistribution Under Progressive Lumbar Disc Degeneration

**Authors:** Oleg Ardatov, Sofia Rita Fernandes, Artūras Kilikevičius, Vidmantas Alekna

PMC · DOI: 10.3390/bioengineering13020234 · Bioengineering · 2026-02-17

## TL;DR

This study uses computer models to understand how spinal disc degeneration affects load distribution in the lower back.

## Contribution

A parametric finite element model is introduced to simulate progressive lumbar disc degeneration and its biomechanical consequences.

## Key findings

- Severe disc degeneration increases annulus fibrosus stresses by up to 175%.
- Nucleus pulposus stress decreases by ~70% in severe degeneration.
- Model predictions align with cadaveric and in vivo data on intradiscal pressure changes.

## Abstract

This study presents a finite element (FE) investigation of intervertebral disc (IVD) degeneration in the human lumbar spine (L1–L3 segment). The model, based on CT-derived geometry and isotropic hyperelastic representation of disc tissues, incorporates controlled simplifications, detailed in the limitations section. Degenerative changes were parametrically simulated across healthy, mild, moderate, and severe stages by reducing disc height (up to 60%), nucleus pulposus volume (up to 70%), and adjusting tissue stiffness to reflect dehydration and fibrosis. Displacement-controlled compressive loading was applied to assess von Mises stress distributions, reaction forces, and load transfer mechanisms. Results indicate significant load redistribution: annulus fibrosus stresses increased by up to 175% in severe degeneration, while nucleus pulposus stresses decreased by ~70%, indicating a diminished compressive load-bearing contribution of the nucleus. Model predictions were validated against cadaveric and in vivo data, confirming trends in intradiscal pressure (IDP) reductions (40–70%) and stress elevations. The parametric framework elucidates interactions between geometric and material changes, providing clinicians with insights into degeneration progression and guiding biomedical engineers in implant design and interventions.

## Full-text entities

- **Genes:** IDH1 (isocitrate dehydrogenase (NADP(+)) 1) [NCBI Gene 3417] {aka HEL-216, HEL-S-26, IDCD, IDH, IDP, IDPC}
- **Diseases:** fibrosis (MESH:D005355), injury to (MESH:D014947), calcification (MESH:D002114), disc height (MESH:C000719188), sclerosis (MESH:D012598), cartilage loss (MESH:D002357), tears (MESH:D012167), nucleus pulposus (MESH:C537927), osteoarthritis (MESH:D010003), Lumbar Disc Degeneration (MESH:C535531), endplate damage (MESH:C566415), vertebral osteoporosis (MESH:D010024), dehydration (MESH:D003681), AF (OMIM:614822), Degeneration of the intervertebral disc (MESH:D055959), degenerated (MESH:D009410), kyphotic deformity (MESH:D009140), herniation (MESH:D004677)
- **Chemicals:** Water (MESH:D014867)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12938578/full.md

## References

47 references — full list in the complete paper: https://tomesphere.com/paper/PMC12938578/full.md

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Source: https://tomesphere.com/paper/PMC12938578