Sobański Dawid, Staszkiewicz Rafał, Sobańska Małgorzata, Strojny Damian, Grabarek Beniamin Oskar
Department of Neurosurgery, Szpital sw. Rafala in Cracow, Cracow, Poland.
Collegium Medicum, WSB University, Dabrowa Gornicza, Poland.
Mol Pain. 2025 Jan-Dec;21:17448069241309001. doi: 10.1177/17448069241309001.
This study investigated the role of brain-derived neurotrophic factor (BDNF) in patients with degenerative lumbar stenosis, focusing on its expression and correlation with pain intensity. The study examined 96 patients with lumbar stenosis and 85 control participants. BDNF levels in the yellow ligamentum flavum were measured using reverse transcription quantitative polymerase chain reaction (RT-qPCR), enzyme-linked immunosorbent assay (ELISA), and western blot analysis. The results showed significantly higher BDNF expression at both messenger ribonucleic acid (mRNA; fold change = +1.35 ± 0.23; < 0.05) and protein levels in patients (28.98 ± 6.40 pg/mg) compared to controls (4.56 ± 1.98 pg/mg; < 0.05). Furthermore, BDNF levels correlated positively with pain intensity reported by patients, with higher expression observed in those experiencing more severe pain. The study also explored the influence of lifestyle factors, such as smoking and alcohol consumption, and related diseases, such as diabetes, on BDNF expression. Smoking, alcohol use, and diabetes were associated with significantly elevated BDNF levels ( < 0.05). These findings suggest that BDNF could serve as a biomarker for pain severity in degenerative lumbar stenosis at the protein level, although this was not consistently observed at the mRNA level; this highlights the potential for BDNF-targeted therapies in managing pain. Future research should involve larger longitudinal studies to validate these findings and explore therapeutic interventions. This study underscores the importance of considering molecular and lifestyle factors in the treatment of degenerative lumbar stenosis, aiming to improve patient outcomes through comprehensive, targeted approaches.
本研究调查了脑源性神经营养因子(BDNF)在退行性腰椎管狭窄症患者中的作用,重点关注其表达以及与疼痛强度的相关性。该研究检查了96例腰椎管狭窄症患者和85名对照参与者。使用逆转录定量聚合酶链反应(RT-qPCR)、酶联免疫吸附测定(ELISA)和蛋白质印迹分析来测量黄韧带中的BDNF水平。结果显示,与对照组(4.56±1.98 pg/mg;<0.05)相比,患者的信使核糖核酸(mRNA;倍数变化=+1.35±0.23;<0.05)和蛋白质水平上的BDNF表达均显著更高(28.98±6.40 pg/mg)。此外,BDNF水平与患者报告的疼痛强度呈正相关,在经历更严重疼痛的患者中观察到更高的表达。该研究还探讨了生活方式因素(如吸烟和饮酒)以及相关疾病(如糖尿病)对BDNF表达的影响。吸烟、饮酒和糖尿病与BDNF水平显著升高相关(<0.05)。这些发现表明,BDNF在蛋白质水平上可作为退行性腰椎管狭窄症疼痛严重程度的生物标志物,尽管在mRNA水平上并非始终如此;这突出了针对BDNF的疗法在管理疼痛方面的潜力。未来的研究应包括更大规模的纵向研究,以验证这些发现并探索治疗干预措施。本研究强调了在退行性腰椎管狭窄症治疗中考虑分子和生活方式因素的重要性,旨在通过全面、有针对性的方法改善患者预后。