Department of Biology and Anatomy, Poznan University of Physical Education, Królowej Jadwigi 27/39, 61-871, Poznan, Poland.
Department of Physiology and Biochemistry, Poznan University of Physical Education, 61-871, Poznan, Poland.
BMC Musculoskelet Disord. 2023 Mar 16;24(1):196. doi: 10.1186/s12891-023-06300-5.
Apart from the positive effect of lumbar traction on structural changes within the spine in patients with low back pain, it is likely that therapeutic effects are correlated with pain biomarkers in the blood. Among them, systemic metabolic factors related to obesity may play an important role. This is the first study designed to examine the effectiveness of traction therapy in two experimental groups with considerably different BMI and to assess relationships between blood biomarkers and low back pain intensity.
In the prospective clinical trial, women suffering from chronic low back pain were allocated into the normal-weight or obesity groups. Patients in both groups underwent twenty sessions of lumbar traction therapy (30 min a day, continuous mode with a force level of 25-30% of body weight). Before and after therapy subjective assessments of pain (VAS and PPT) were performed, and serum concentrations of aggrecan chondroitin sulfate 846 epitope (CS-846), neuropeptide Y, leptin, adipsin and growth and differentiation factor 15 (GDF-15) were determined. The data were statistically evaluated for 28 women.
After therapy, the maximal low back pain decreased in both groups, GDF-15 concentration was reduced in the normal-weight group and increased in the obesity group, and CS-846 concentration decreased in the obesity group. The sensation of PPT in the lumbar spine and mean concentrations of neuropeptide Y, leptin and adipsin did not change in both groups. However, the relationships of GDF-15, leptin, and adipsin concentrations with the perception of pain were revealed.
Distinct differences between the normal-weight and obesity groups pointed on the role of excessive adipose tissue in aggravating the inflammatory processes and in the development of low back pain. Adipsin, CS-846 and GDF-15 aspire to be the low back pain biomarkers in women with obesity, but there is a need for further research to answer whether they might be considered reliable biomarkers for the prognosis and monitoring of chronic low back treatment.
NCT04507074, registered prospectively on July 6, 2020.
除了腰椎牵引对腰痛患者脊柱结构变化的积极影响外,治疗效果可能与血液中的疼痛生物标志物相关。其中,与肥胖相关的全身性代谢因素可能发挥重要作用。这是第一项旨在检查两种实验性分组中牵引治疗效果的研究,这两种分组的 BMI 差异很大,并评估血液生物标志物与腰痛强度之间的关系。
在这项前瞻性临床试验中,患有慢性腰痛的女性被分配到正常体重组或肥胖组。两组患者均接受 20 次腰椎牵引治疗(每天 30 分钟,连续模式,力水平为体重的 25-30%)。治疗前后进行主观疼痛评估(VAS 和 PPT),并测定血清中聚集蛋白聚糖硫酸软骨素 846 表位(CS-846)、神经肽 Y、瘦素、脂联素和生长分化因子 15(GDF-15)的浓度。对 28 名女性的数据进行了统计学评估。
治疗后,两组患者的最大腰痛均减轻,正常体重组的 GDF-15 浓度降低,肥胖组的 GDF-15 浓度升高,肥胖组的 CS-846 浓度降低。两组患者的腰椎 PPT 感觉和神经肽 Y、瘦素和脂联素的平均浓度均无变化。然而,揭示了 GDF-15、瘦素和脂联素浓度与疼痛感知之间的关系。
正常体重组和肥胖组之间的明显差异表明,过多的脂肪组织在加重炎症过程和腰痛发展中起作用。脂联素、CS-846 和 GDF-15 有望成为肥胖女性腰痛的生物标志物,但需要进一步研究以回答它们是否可以被认为是慢性腰痛治疗预后和监测的可靠生物标志物。
NCT04507074,于 2020 年 7 月 6 日前瞻性注册。