Background Inflammatory markers play an important role in the pathophysiology of Lumbar disc herniation (LDH). This study presents a comprehensive multi-assessment of the inflammatory landscape by combining serum inflammatory cytokines quantification, their diagnostic performance, associations with radiological features, and integrating the experimental findings into an in-silico protein–protein interaction network.
Methods A multifaceted study design was utilized to quantify and compare the distribution of selected inflammatory cytokines in patients with LDH and control subjects. The diagnostic ability of these cytokines was assessed using receiver operating characteristic curve analysis. The cytokines values were correlated with selected radiological findings including disc herniation subtypes (protrusion, extrusion, and sequestration), and further categorized as contained and non-contained in patients using a Spearman’s rank correlation test. Additionally, computational analysis was performed to identify the central hubs and functionally enriched pathways.
Results In patients with LDH, IL-6 and IL-1β showed statistically significant (IL-6: p < 0.001; IL-1β: p = 0.001) rise, but IL-6 showed high diagnostic and discriminative power (AUC = 0.99; cut-off: 19.99 pg/mL). Further IL-1β exhibited a positive correlation with non-contained disc herniation (extrusion and sequestration), while displaying a significant (p < 0.05) negative correlation with protrusion. In silico analysis identified IL-1β, IL-8, TNF-α, IL-6, IL-1α, CSF2, CSF3, and IL-10 as central hubs, with IL-1β being the top ranked hub in determining functionally enriched cytokine-cytokine receptor interaction.
Conclusions Study confirmed IL-6 as a powerful diagnostic marker for LDH, while IL-1β aids in determining contained and non-contained disc herniation. Further, IL-1β was identified as the central hub, triggering functionally enriched pathways in the pathogenesis of LDH.
Competing Interest StatementThe authors have declared no competing interest.
Funding StatementYes
Author DeclarationsI confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.
Yes
The details of the IRB/oversight body that provided approval or exemption for the research described are given below:
Ethical approval was obtained Ethics review committee of Faculty of Medical Sciences, University of Sri Jayewardenepura and written informed consent was obtained. Patient details will be maintained at high confidentiality, etc
I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.
Yes
I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).
Yes
I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.
Yes
Data AvailabilityAll relevant data are within the manuscript and its Supporting Information files. Additional data underlying the findings of this study are available from the corresponding author upon reasonable request with limitations, however no individual identifiers will be provided. Data cannot be made publicly available due to ethical restrictions involving human participants, as imposed by the Ethics Review Committee of the University of Sri Jayewardenepura.
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