Enzymatic denaturation versus excessive fatigue loading degeneration: Effects on the time-dependent response of the intervertebral disc

• Published in: Journal of biomechanics Vol. 171; p. 112159
• Main Authors: Nikkhoo, Mohammad, Wang, Jaw-Lin, Cheng, Chih-Hsiu, Parnianpour, Mohamad, Khalaf, Kinda
• Format: Journal Article
• Language: English
• Published: United States Elsevier Ltd 01.06.2024; Elsevier Limited
• Subjects: Cyclic loads; Deformation resistance; Degeneration; Degeneration animal models; Degenerative disc disease; Degenerative diseases; Denaturation; Enzymatic denaturation; Extracellular matrix; Fatigue; Finite element modeling; Frequency dependence; In-vitro experiments; Intervertebral disc; Intervertebral discs; Low back pain; Materials fatigue; Mechanical properties; Phenotypes; Physiology; Proteoglycans; Software; Swine; Thorax; Time dependence; Trypsin; United States > US; Enzymatic denaturation; Fatigue; Degeneration animal models; Finite element modeling; In-vitro experiments; Intervertebral disc
• ISSN: 0021-9290; 1873-2380; 1873-2380
• DOI: 10.1016/j.jbiomech.2024.112159

Degenerative disc disease (DDD), regardless of its phenotype and clinical grade, is widely associated with low back pain (LBP), which remains the single leading cause of disability worldwide. This work provides a quantitative methodology for comparatively investigating artificial IVD degeneration via two popular approaches: enzymatic denaturation and fatigue loading. An in-vitro animal study was used to study the time-dependent responses of forty fresh juvenile porcine thoracic IVDs in conjunction with inverse and forward finite element (FE) simulations. The IVDs were dissected from 6-month-old-juvenile pigs and equally assigned to 5 groups (intact, denatured, low-level, medium-level, high-level fatigue loading). Upon preloading, a sinusoid cyclic load (Peak-to-peak/0.1-to-0.8 MPa) was applied (0.01–10 Hz), and dynamic-mechanical-analyses (DMA) was performed. The DMA outcomes were integrated with a robust meta-model analysis to quantify the poroelastic IVD characteristics, while specimen-specific FE models were developed to study the detailed responses. The results demonstrated that enzymatic denaturation had a more significantly pronounced effect on the resistive strength and shock attenuation capabilities of the intervertebral discs. This can be attributed to the simultaneous disruption of the collagen fibers and water-proteoglycan bonds induced by trypsin digestion. Fatigue loading, on the other hand, primarily influenced the disc’s resistance to deformation in a frequency-dependent pattern, where alterations were most noticeable at low loading frequencies. This study confirms the intricate interplay between the biochemical changes induced by enzymatic processes and the mechanical behavior stemming from fatigue loading, suggesting the need for a comprehensive approach to closely mimic the interrelated multifaceted processes of human disc degeneration.