Department of Orthopaedic Surgery, Stanford University, Palo Alto, CA, USA.
Spine (Phila Pa 1976). 2011 Aug 15;36(18):1464-9. doi: 10.1097/BRS.0b013e3181f40e88.
A single-center, prospective, consecutive case series of patients undergoing epidural lavage before the treatment of radiculopathy due to lumbar disc herniation.
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).
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.
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.
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.
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.
一项单中心、前瞻性、连续病例系列研究,纳入了在接受腰椎间盘突出症神经根病治疗前接受硬膜外灌洗的患者。
确定纤维连接蛋白和聚集蛋白聚糖的新型复合物是否可预测硬膜外类固醇注射(ESI)治疗腰椎间盘突出症引起的神经根病的临床反应。
尽管 ESI 对该适应证的疗效存在差异,但因其治疗腰椎神经根病的应用仍很广泛。随着对成本控制的关注增加,确定哪些患者可能从中受益将是有益的。目前,尚无准确的诊断测试可预测腰痛和坐骨神经痛综合征中 ESI 的反应。我们之前研究过与神经根病相关的椎间盘退变的生物标志物。
我们着手确定纤维连接蛋白和聚集蛋白聚糖的分子复合物是否可预测 ESI 治疗腰椎间盘突出症引起的神经根病的临床反应。这项前瞻性研究在一家单中心进行,纳入了 26 例有神经根痛且 MRI 显示阳性的腰椎间盘突出症患者,这些患者选择了 ESI。在 ESI 前立即进行硬膜外生理盐水灌洗。使用异质夹心酶联免疫吸附试验测定灌洗液中的纤维连接蛋白-聚集蛋白聚糖复合物(FAC)。将结果与基线时注射后医疗结局研究 36 项简明健康调查量表(SF-36)中物理成分综合评分(PCS)的间隔改善进行比较。
有 FAC 的患者的平均基线 PCS 改善为 22.9(SD,12.4),而无复合物的患者为 0.64(SD,3.97;P<0.001)。SF-36 总改善的差异也具有高度显著性(P<0.001)。通过受试者工作特征分析(曲线下面积=0.97;P<0.001),FAC 的存在可预测腰椎 ESI 后 PCS 有临床意义的增加。在有无标志物的组之间,年龄(P=0.25)、性别(P=0.84)、侧别(P=0.06)、腰椎节段(P=0.75)或支付类型(工人补偿与私人保险;P=0.90)无显著差异。
纤维连接蛋白和聚集蛋白聚糖的分子复合物可预测腰椎间盘突出症神经根病患者对腰椎 ESI 的反应。在本系列中,该生物标志物准确、客观,不受人口统计学或社会心理变量的影响。