PMID- 31659847 OWN - NLM STAT- MEDLINE DCOM- 20210802 LR - 20210802 IS - 1934-1563 (Electronic) IS - 1934-1482 (Linking) VI - 12 IP - 7 DP - 2020 Jul TI - Predicting Response to Epidural Steroid Injections for Lumbar Spinal Stenosis with Biomarkers and Electromyography. PG - 663-670 LID - 10.1002/pmrj.12272 [doi] AB - BACKGROUND: Epidural steroid injections (ESIs) may be beneficial for lumbar spinal stenosis (LSS) symptoms. Past studies found interferon-gamma, fibronectin-aggrecan complex, and electromyography (EMG) to predict patients' response to ESIs for other spinal pathologies, but no similar studies have been done for LSS. OBJECTIVE: To explore the ability of biomarkers and EMG to help predict outcome after ESI in LSS. DESIGN: Prospective observational cohort. SETTING: The physical medicine & rehabilitation spine clinic at a tertiary care center. PARTICIPANTS: Eleven patients with LSS were recruited from the spine clinic at a Veterans Affairs Medical Center. INTERVENTIONS: Participants underwent one interlaminar ESI. Before ESI, the following data were collected: pain intensity on visual analog scale (VAS), disability via the Pain Disability Questionnaire (PDQ) and LSS symptoms via the Swiss Spinal Stenosis Questionnaire (SSSQ), serum high-sensitivity C-reactive protein level, standard diagnostic EMG, assay of epidural lavasate (epidural saline lavage performed immediately prior to ESI) and serum cytokine biomarkers indicative of inflammation. OUTCOME MEASURES: Leg pain intensity (VAS), disability (PDQ), LSS symptoms (SSSQ) and satisfaction (SSSQ satisfaction subscale) were assessed at 1 and 2 months following ESI. Pearson correlational coefficients were calculated between independent variables and outcome measures. RESULTS: Serum monocyte chemoattractant protein-1 (MCP-1) level positively correlated with improvement on 2-month satisfaction. Abnormal EMG finding of radiculopathy positively correlated with improvement in PDQ score at 1 month. Epidural cytokine levels were not detectable in most samples, except for scattered marginally elevated levels in a few cytokines such as MCP-1, RANTES (Regulated on Activation, Normal T Cell Expressed and Secreted) and interleukin-1b. CONCLUSIONS: This exploratory pilot study revealed that some biomarkers and EMG findings indicative of inflammation and nerve root injury may be predictive of improvement following ESI in patients with LSS. The results of this study will be used to inform a fully powered study to further evaluate these relationships in LSS patients. CI - (c) 2019 American Academy of Physical Medicine and Rehabilitation. This article has been contributed to by US Government employees and their work is in the public domain in the USA. FAU - Lin, Chung-Kuang AU - Lin CK AD - UT Southwestern Medical Center, Dallas, TX. FAU - Borresen, Aleksander AU - Borresen A AD - Department of Physical Medicine & Rehabilitation, University of Alabama at Birmingham, Birmingham, AL. FAU - Kroll, Mitchell AU - Kroll M AD - Dallas VA Research Corporation, VA North Texas Health Care System, Dallas, TX. FAU - Annaswamy, Thiru M AU - Annaswamy TM AUID- ORCID: 0000-0002-3969-9221 AD - Dallas VA Research Corporation, VA North Texas Health Care System, Dallas VA Medical Center, Dallas, TX. AD - Department of PM&R, UT Southwestern Medical Center, Dallas, TX. LA - eng SI - ClinicalTrials.gov/NCT03511053 PT - Journal Article PT - Observational Study PT - Research Support, Non-U.S. Gov't DEP - 20191228 PL - United States TA - PM R JT - PM & R : the journal of injury, function, and rehabilitation JID - 101491319 RN - 0 (Biomarkers) RN - 0 (Cytokines) RN - 0 (Steroids) SB - IM MH - Biomarkers/blood MH - Cytokines/blood MH - Electromyography MH - Humans MH - *Injections, Epidural MH - Lumbosacral Region MH - Patient Satisfaction MH - Pilot Projects MH - Prospective Studies MH - Rehabilitation Centers MH - *Spinal Stenosis/complications/drug therapy MH - *Steroids/therapeutic use MH - Tertiary Care Centers MH - Treatment Outcome EDAT- 2019/10/30 06:00 MHDA- 2021/08/03 06:00 CRDT- 2019/10/30 06:00 PHST- 2019/04/23 00:00 [received] PHST- 2019/10/21 00:00 [accepted] PHST- 2019/10/30 06:00 [pubmed] PHST- 2021/08/03 06:00 [medline] PHST- 2019/10/30 06:00 [entrez] AID - 10.1002/pmrj.12272 [doi] PST - ppublish SO - PM R. 2020 Jul;12(7):663-670. doi: 10.1002/pmrj.12272. Epub 2019 Dec 28.