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IFN-γ Correlations with Pain Assessment, Radiological Findings, and Clinical Intercourse in Patient after Lumbar
Piotr Kamieniak1, Joanna M Bielewicz2, Cezary Grochowski1,3
1Department of Neurosurgery, Medical University of Lublin, Poland.
Disease Markers
|October 28, 2020
Summary
Reduced back pain after lumbar microdiscectomy correlates with lower serum interferon gamma (IFN-γ) levels. This finding suggests a role for IFN-γ in sciatica pain mechanisms and offers insights into radicular pain development.
Area of Science:
- Neuroscience
- Immunology
- Orthopedic Surgery
Background:
- Sciatica pain, often caused by lumbar disc herniations, is frequently treated with microdiscectomy.
- Interferon gamma (IFN-γ), a pro-inflammatory cytokine, has been implicated in pain development, but its specific role in radicular pain remains unclear.
Purpose of the Study:
- To investigate the relationship between pain reduction following lumbar microdiscectomy and serum levels of interferon gamma (IFN-γ).
- To explore the potential role of IFN-γ in the pathophysiology of sciatica and radicular pain.
Main Methods:
- Clinical and immunoenzymatic assessments were conducted on 27 patients before and 3 months after lumbar microdiscectomy.
- Pain was evaluated using the Numeric Rating Scale (NRS), McGill Pain Questionnaire (SF-MPQ), Oswestry Disability Index (ODI), and Beck Depression Inventory (BDI).
- Plasma concentrations of IFN-γ were measured using an immunoenzymatic method.
Main Results:
- Significant positive correlations were observed between pain scores (NRS, PRI) and IFN-γ levels both before and after surgery, indicating that lower pain is associated with lower IFN-γ.
- Patients with nerve compression showed significantly lower IFN-γ levels before and after surgery compared to those without nerve compression.
Conclusions:
- A decrease in pain after lumbar microdiscectomy is correlated with reduced serum IFN-γ levels.
- Elevated IFN-γ levels were observed in patients without significant nerve compression, suggesting a complex role in radicular pain mechanisms.

