Evaluation of the Neuropathic Component of Chronic Low Back Pain
Language English Country United States Media print
Document type Journal Article, Observational Study, Research Support, Non-U.S. Gov't
- MeSH
- Biopsy MeSH
- Adult MeSH
- Spinal Cord Compression complications MeSH
- Skin pathology MeSH
- Middle Aged MeSH
- Humans MeSH
- Low Back Pain complications diagnosis pathology MeSH
- Pain Measurement MeSH
- Spinal Nerve Roots pathology MeSH
- Young Adult MeSH
- Nerve Fibers pathology MeSH
- Neuralgia complications diagnosis pathology MeSH
- Neurologic Examination MeSH
- Sensation Disorders diagnosis etiology MeSH
- Cross-Sectional Studies MeSH
- Radiculopathy etiology pathology MeSH
- Aged MeSH
- Spinal Stenosis complications MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Young Adult MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Observational Study MeSH
- Research Support, Non-U.S. Gov't MeSH
OBJECTIVES: Assessment of neuropathic pain in chronic low back syndromes is important. However, there is currently no gold standard for its diagnosis. The aim of this observational cross-sectional study was to assess the neuropathic component of pain in various chronic low back pain syndromes using a range of diagnostic tests. MATERIALS AND METHODS: Included in this study were 63 patients with chronic axial low back pain (ALBP), 48 patients with chronic radicular syndromes (CRS) comprising 23 with discogenic compression (CDRS) and 25 with lumbar spinal stenosis (LSS), and 74 controls. PainDETECT questionnaire (PDQ), quantitative sensory testing (QST), and skin biopsy with evaluation of intraepidermal nerve fiber density (IENFD) were used to assess the neuropathic pain component. RESULTS: Positive PDQ (≥19) was obtained more frequently in patients with CDRS and LSS (26.1% and 12.0%, respectively) compared with patients with ALBP (1.6%, P<0.001). The proportion of patients with sensory loss confirmed by QST was lowest in the ALBP subgroup (23.8%) compared with CDRS (47.8%), and LSS (68.0%) subgroups (P<0.001). A reduction in IENFD was disclosed in a proportion of up to 52.0% of affected roots in patients with CRS. DISCUSSION: Neuropathic pain is quite frequent in CRS, and QST reveals sensory loss as a frequent abnormality in patients with CRS. Using a cut-off value of 19, PDQ identified a neuropathic component in a relatively low proportion of patients with CRS. CRS may be associated with a reduction in IENFD.
CEITEC Central European Institute of Technology
Department of Neurology University Hospital and Masaryk University Brno
Institute of Biostatistics and Analyses Faculty of Medicine Masaryk University Brno Czech Republic
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