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Outcome of lumbar epidural steroid injection is predicted by assay of a complex of fibronectin and aggrecan from epidural lavage.

机译:通过测定硬膜外灌洗液中纤连蛋白和聚集蛋白聚糖的复合物可预测腰椎硬膜外类固醇注射的结果。

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STUDY DESIGN: A single-center, prospective, consecutive case series of patients undergoing epidural lavage before the treatment of radiculopathy due to lumbar disc herniation. OBJECTIVE: To determine whether a novel complex of fibronectin and aggrecan predicts clinical response to epidural steroid injection (ESI) for the indication of radiculopathy from lumbar herniated nucleus pulposus (HNP). SUMMARY OF BACKGROUND DATA: ESI for lumbar radiculopathy due to HNP is widely used despite variable effectiveness for this indication. With increased attention aimed at cost containment, it would be beneficial to identify those in whom ESI may be helpful. There are currently no accurate diagnostic tests to predict response to ESI in back pain and sciatica syndromes. We have previously investigated biomarkers of disc degeneration associated with radiculopathy. METHODS: We embarked to determine whether a molecular complex of fibronectin and aggrecan predicts clinical response to ESI for the indication of radiculopathy from HNP. This prospective study was conducted at a single center and included 26 patients with radiculopathic pain and magnetic resonance imaging positive for HNP, who elected ESI. Epidural lavage with physiologic saline was performed immediately before ESI. The lavage fluid was assayed for the fibronectin-aggrecan complex (FAC) by using a heterogeneous sandwich enzyme-linked immunosorbent assay. The results were compared with the interval improvement in the physical component summary (PCS) score of the Medical Outcomes Study Short Form-36 instrument (SF-36) after injection compared with baseline. RESULTS: The mean improvement from baseline PCS in patients with the FAC was 22.9 (SD, 12.4) and without the complex was 0.64 (SD, 3.97; P < 0.001). Differences in total SF-36 improvement were also highly significant (P < 0.001). The presence of the FAC predicts a clinically significant increase in PCS after lumbar ESI by receiver-operating-characteristic analysis (area under the curve = 0.97; P < 0.001). There was no significant difference in age (P = 0.25), sex (P = 0.84), laterality (P = 0.06), lumbar spinal level (P = 0.75), or payer type (worker's compensation vs. private insurance; P = 0.90) between groups with and without the marker. CONCLUSION: A molecular complex of fibronectin and aggrecan predicts response to lumbar ESI for radiculopathy with HNP. The biomarker is accurate, objective, and not affected by demographic or psychosocial variables in this series.
机译:研究设计:单中心,前瞻性,连续病例系列患者,由于腰椎间盘突出症在神经根病治疗之前接受硬膜外灌洗。目的:确定纤连蛋白和聚集蛋白聚糖的新型复合物能否预测硬膜外类固醇注射(ESI)的临床反应,以指示腰椎间盘髓核(HNP)神经根病变。背景数据概述:尽管针对该适应症的疗效存在差异,但由于HNP引起的腰神经根病的ESI被广泛使用。随着越来越多的人关注控制成本,确定那些可能对ESI有所帮助的人将是有益的。当前尚无准确的诊断测试可预测背痛和坐骨神经痛综合征对ESI的反应。我们之前已经研究了与神经根疾病相关的椎间盘退变的生物标志物。方法:我们着手确定纤连蛋白和聚集蛋白聚糖的分子复合物是否可预测ESI的临床反应,以指示HNP引起的神经根病。这项前瞻性研究在单个中心进行,纳入了26名放射神经性疼痛和HNP阳性的磁共振成像患者,他们选择了ESI。在ESI之前立即用生理盐水进行硬膜外灌洗。通过使用异质夹心酶联免疫吸附测定法测定灌洗液中的纤连蛋白-aggrecan复合物(FAC)。将结果与注射后与基线相比医学结果研究简短表格36器械(SF-36)的物理成分摘要(PCS)评分的间隔改善进行比较。结果:FAC患者基线PCS的平均改善为22.9(SD,12.4),无复合物的患者为0.64(SD,3.97; P <0.001)。 SF-36总改善的差异也非常显着(P <0.001)。 FAC的存在通过接受者操作特征分析预测腰椎ESI后PCS的临床显着增加(曲线下面积= 0.97; P <0.001)。年龄(P = 0.25),性别(P = 0.84),侧卧感(P = 0.06),腰椎水平(P = 0.75)或付款人类型(工人的报酬与私人保险; P = 0.90)没有显着差异。 )在带有和不带有标记的组之间。结论:纤连蛋白和聚集蛋白聚糖的分子复合物可预测HNP致神经根病对腰椎ESI的反应。该生物标志物准确,客观,不受本系列人口统计学或社会心理变量的影响。

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