Cytokines, Neuroplasticity Modulators, and Biomarkers in Spinal Canal Stenosis and Endoscopic Decompression

Spinal stenosis is a common musculoskeletal disorder that causes pain or disability in patients. However, the pathogenesis of this disease is complex and has not yet been fully elucidated. Lumbar spinal canal stenosis results from degenerative changes in structures located behind the spinal cord, such as hypertrophy of the ligamentum flavum (LF), as well as ligament calcification, degeneration and hypertrophy of the facet joints and/or herniation of intervertebral discs located anterior to the spinal cord. The pathology of LF hypertrophy includes fibrocartilaginous changes associated with type II collagen proliferation, ossification, calcium crystal deposition, degeneration of collagen and elastic fibers, and chondroid metaplasia of ligament fibroblasts. Numerous scientific studies have attempted to explore the etiology of hypertrophy and ossification of spinal ligaments, considering systemic, local, genetic, and environmental factors. However, the mechanism of degeneration development is still not fully understood. Besides mechanical stress and increased collagen synthesis (fibrosis) in the ligament, which make age a major risk factor, the presence of inflammation and macrophage infiltration is considered a significant contributor to degeneration development.

Therefore, it is reasonable to assume that the presence of inflammation associated with other health conditions-especially chronic ones-may, to an unknown extent, influence the course of spinal structure degeneration. Currently, obesity and sarcopenia are drawing particular attention as disorders affecting all systems of the human body. Since their prevalence is increasing, a thorough understanding of their consequences on individual organs has significant social and practical importance for prevention and health protection.

An increasing number of reports indicate that disturbances in lipid metabolism and the secretion of pro-inflammatory adipokines and cytokines are deeply involved in regulating cellular phenotypes and fates, extracellular matrix metabolism, and inflammation in the pathophysiological processes of degenerative spinal and joint diseases. Metabolic disorders can affect bone metabolism and lead to ectopic ossification and fat deposition not only in spinal ligaments but also in other spinal structures. Also noteworthy is the influence of the adipokinome on the development of musculoskeletal degenerative disorders. Even anatomically present epidural fat in the spinal canal may become inflamed and spontaneously secrete inflammatory cytokines, potentially modifying the function of adjacent tissues, such as paraspinal muscles and ligaments. It is worth mentioning that spinal epidural lipomatosis, characterized by an excess of fat tissue in the epidural space leading to spinal canal stenosis, is strongly associated with obesity.

So far, it has been confirmed that adipokines and their receptors, although primarily located in white adipose tissue, are also present in joint cartilage and spinal bone marrow. Adipokines may promote ligamentum flavum degeneration by stimulating inflammatory responses and promoting pathological changes. Leptin has been shown to significantly correlate with the number of vertebrae affected by ligamentous ossification. Fan et al. discovered that leptin markedly upregulates alkaline phosphatase and osteocalcin mRNA expression in ligamentum flavum cells. High levels of visfatin have also been found in the ligamenta flava of patients with confirmed ossification. There is no available data on the presence and role of other adipose tissue-derived cytokines such as adipsin, vaspin, resistin, lipocalin-2, progranulin, chemerin, omentin-1, or growth differentiation factor-15 (GDF-15) in the ligamentum flavum. It is highly likely that these cytokines are also involved in the development of spinal canal stenosis, which constitutes our research hypothesis. The presence and levels of these cytokines in epidural fat tissue in patients with stenosis, compared to those without spinal canal narrowing, have not been studied to date. Since studies confirm that chronic systemic inflammation affects various tissues and local inflammation significantly affects neighboring structures, we hypothesize that ligaments, paraspinal muscles, intervertebral discs, etc., may be particularly vulnerable to cytokines secreted by epidural fat tissue. Previous in vitro studies confirmed that a local environment rich in cytokines such as IL-6, IL-1α, nitric oxide donor (SNAP), and prostaglandin E2 changes the gene expression of collagens I, V, XI, and osteocalcin in ligamentum flavum cells. However, the impact of the mentioned adipokines on the development of ligamentum flavum degeneration has not yet been determined.

The study will involve examining the concentrations of cytokines (especially adipokines) and neuroplasticity modulators and their mRNA expression in tissues routinely removed from patients with spinal stenosis and disc herniation during surgery, as well as collecting blood from patients twice, before the procedure and during a follow-up visit two months after the procedure.

Objectives

1. To identify differences in selected biomarker concentrations in samples of ligamentum flavum, paraspinal muscles, and epidural fat collected from the lumbar region of patients with stenosis compared to those without spinal canal degeneration.
2. To determine whether the expression of selected biomarkers in tissues correlates with their presence in the patients' blood and whether they relate to the degree of degeneration, disability, pain intensity, and body mass.
3. To select potential biomarkers for monitoring the effectiveness of spinal canal decompression surgery by comparing biomarker levels before surgery and two months into recovery.
4. To identify potential proteins that modulate metabolism and inflammation in the ligamentum flavum.
5. To evaluate the impact of selected cytokines and adipokinome of epidural fat tissue on metabolism and inflammation in ligamentum flavum cell cultures.

Study Population Description

The study will involve 100 patients from the Orthopaedic-Rehabilitation Clinical Hospital of the Poznań University of Medical Sciences, including both men and women:

• 50 patients with lumbar spinal canal stenosis, aged 40-90 years
• 50 patients with intervertebral disc herniation, aged 18-40 years, requiring surgical treatment Participants will undergo surgery provided they give informed consent to use their tissues in scientific research.
• The study group will undergo endoscopic spinal canal decompression, involving the removal of tissues (bone, ligament, joint) compressing neural structures, and possibly removing a displaced intervertebral disc fragment.
• The control group will undergo isolated intervertebral disc herniation surgery, involving the removal of the displaced disc fragment.

Methods Before surgery (within 48h) and two months post-op, 20 ml of venous blood will be drawn from each patient.

During surgery, the following samples will be collected:

• Paraspinal muscle tissue
• Ligamentum flavum
• Epidural fat tissue

The study will use the following methods/tools:

1. Standardized questionnaires for disability and pain intensity
2. MRI of the lumbar spine (routinely performed before surgery)

3. Molecular testing

   1. mRNA expression of cytokines (GDF-15, adipsin, vaspin, resistin, lipocalin-2, progranulin, chemerin, omentin-1) will be measured using PCR.
   2. Immunoassays using commercial ELISA kits will be performed on tissue homogenates and serum to determine proteins concentrations (GDF-15, adipsin, vaspin, resistin, lipocalin-2, progranulin, chemerin, omentin-1)
4. Cell culture and stimulation of cells with cytokines and medium obtained from adipose tissue One-third of the biological material will be allocated for cell culture studies. Samples of the ligamentum flavum, paraspinal muscles, and epidural adipose tissue will be collected directly after surgery and placed in sterile containers with appropriate transport media.

All samples will be immediately transported to the cell culture laboratory under sterile conditions, in the shortest possible time from collection. Upon arrival at the laboratory, they will undergo appropriate, pre-established cell isolation protocols, tailored to the characteristics of each tissue type.

After the exposure period, the expression of mRNA and protein levels of cytokines, fibrosis markers, bone markers, extracellular matrix proteins, matrix degradation enzymes will be measured in the conditioned medium collected from the cultures of myocytes and ligamentum flavum fibroblasts.