Ligament flavum

黄韧带
  • 文章类型: Journal Article
    目的:分析肥大黄韧带(HLF)与正常韧带相比的差异转录组表达。
    方法:进行了一项病例对照研究,包括15例LF肥大患者和15例对照。通过腰椎椎板切除术获得LF样品,并通过DNA微阵列和组织学进行分析。失调的生物过程,信号通路,使用生物信息学工具鉴定HLF中的病理标记物。
    结果:HLF有明显的组织学改变,包括透明病,白细胞浸润,和胶原纤维的排列。转录组分析表明,上调基因与RhoGTPases的信号通路有关,受体酪氨酸激酶(RTK),成纤维细胞生长因子(FGF),WNT,血管内皮生长因子,磷酸肌醇3-激酶(PIK3),丝裂原活化蛋白激酶,和免疫系统。PIK3R1,RHOA,RPS27A,CDC42、VAV1和FGF5、9、18和19被突出显示为HLF中的关键标志物。HLF中的低表达基因与RNA和蛋白质的代谢有关。
    结论:我们的结果表明,肥大型LF的异常过程是由RhoGTP酶的相互作用介导的,RTK,和PI3K通路,以前在HLF中没有描述过,但目前有治疗建议。需要更多的研究来证实我们结果中描述的途径和介质的治疗潜力。
    To analyze the differential transcriptome expression in hypertrophic ligaments flavum (HLF) compared to normal ligaments.
    A case-control study was conducted that included 15 patients with hypertrophy of LF and 15 controls. Samples of LF were obtained through a lumbar laminectomy and analyzed by DNA microarrays and histology. The dysregulated biological processes, signaling pathways, and pathological markers in the HLF were identified using bioinformatics tools.
    The HLF had notable histological alterations, including hyalinosis, leukocyte infiltration, and disarrangement of collagen fibers. Transcriptomic analysis showed that up-regulated genes were associated with the signaling pathways of Rho GTPases, receptor tyrosine kinases (RTK), fibroblast growth factors (FGF), WNT, vascular endothelial growth factor, phosphoinositide 3-kinase (PIK3), mitogen-activated protein kinases, and immune system. The genes PIK3R1, RHOA, RPS27A, CDC42, VAV1, and FGF5, 9, 18, and 19 were highlighted as crucial markers in HLF. The down-expressed genes in the HLF had associations with the metabolism of RNA and proteins.
    Our results suggest that abnormal processes in hypertrophied LF are mediated by the interaction of the Rho GTPase, RTK, and PI3K pathways, which have not been previously described in the HLF, but for which there are currently therapeutic proposals. More studies are required to confirm the therapeutic potential of the pathways and mediators described in our results.
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  • 文章类型: Journal Article
    目的:斜向腰椎椎间融合术(OLIF)包括将大笼插入椎间椎间盘间隙。这通过拉伸黄韧带和释放小关节来扩大椎管和神经孔,导致间接神经减压。我们的目的是研究OLIF后椎管和黄韧带随时间的变化。
    方法:这是一项前瞻性观察性研究,涉及2015年至2018年期间接受OLIFL4-5治疗的30例患者。总的来说,30例患者中有27例接受术前检查,早期随访(<5天),和后期随访(10-14个月)磁共振成像测量椎管和黄韧带的面积。根据结果,将患者分为沉降组和非沉降组进行进一步分析.
    结果:在OLIF之后,术前椎管面积逐渐增大,术后早期,和术后后期(p<0.001)。黄韧带的厚度和面积在相同时期内逐渐减少(p<0.001)。低度沉降(2-4.4mm)不会影响对椎管和韧带的影响。
    结论:在OLIF之后,椎管和黄韧带逐渐改变,这是有效的间接神经减压。此外,低度沉降对椎管和黄韧带重塑的影响不明显。
    OBJECTIVE: Oblique lumbar interbody fusion (OLIF) involves inserting large cages into the interbody disc space. This expands the spinal canal and neural foramen by stretching the ligament flavum and releasing the facet joint, resulting in indirect neural decompression. Our objective was to investigate the changes in the spinal canal and ligament flavum over time after OLIF.
    METHODS: This was a prospective observational study involving 30 patients who underwent OLIF L4-5 between 2015 and 2018. In total, 27 of the 30 patients underwent preoperative, early follow-up ( < 5 days), and late follow-up (10-14 months) magnetic resonance imaging to measure the area of the spinal canal and ligament flavum. Based on the results, the patients were divided into subsidence and nonsubsidence groups for further analysis.
    RESULTS: After OLIF, the spinal canal area gradually increased during the preoperative, early postoperative, and late postoperative periods (p < 0.001). The thickness and area of the ligament flavum decreased gradually over the same periods (p < 0.001). Low-grade subsidence (2-4.4 mm) did not influence the effects on the spinal canal and ligament.
    CONCLUSIONS: After OLIF, the spinal canal and ligament flavum gradually change, which is effective for indirect neural decompression. In addition, the effects of low-grade subsidence on the remodeling of the spinal canal and ligament flavum are insignificant.
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  • 文章类型: Journal Article
    Ligamentum flavum (LF) hypertrophy plays a dominant role in lumbar spinal stenosis (LSS). A previous study found that fibroblast growth factor 9 (FGF9) was upregulated with mechanical stress in rabbit LF. However, the expression and function of FGF9 are not well understood in human LF.
    To evaluate FGF9 expression and function in human LF with and without hypertrophy.
    This study employed a basic research study design utilizing human LF tissue for histological analyses.
    Hypertrophied LF tissue sample from patients with LSS, and nonhypertrophied (control) LFs from patients with lumbar disc herniation or other diseases were obtained during surgery.
    LF specimens were histologically analyzed for FGF9 and vascular endothelial growth factor A (VEGF-A) by immunohistochemistry. The number of total and FGF9 immuno-positive cells and blood vessels were counted and compared between LF with and without hypertrophy. For functional analysis, the effect of FGF9 on cell proliferation and migration was examined using a primary cell culture of human LF.
    Histological studies revealed that the total cell number was significantly higher in the LF of patients with LSS than in the LF of control patients. Immunohistochemistry showed that the percentage of FGF9-positive cells was significantly higher in the LF of patients with LSS than in the controls, and it positively correlated with patients\' age, regardless of disease. Double immune-positive cells for FGF9 and VEGF-A were often observed in vascular endothelial cells and fibroblasts in the fibrotic area of hypertrophied LF, and the number of double positive vessels was significantly higher in LF of LSS patients than in the LF of controls. Primary cell culture of human LF revealed that FGF9 promoted the proliferation and migration of LF cells.
    The present study demonstrated that FGF9 expression is highly upregulated in hypertrophied human LF. FGF9 potentially plays a pivotal role in the process of hypertrophy of LF, which is associated with mechanical stress, through cell proliferation and migration.
    The results from this study partially reveal the molecular mechanisms of LF hypertrophy and suggest that FGF9 may be involved in the process of LF degeneration in elderly patients.
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  • 文章类型: Journal Article
    OBJECTIVE: A prospective, randomized, controlled clinical study was conducted with surgery performed by the same surgeon. The aim was to present a new technique for preserving the ligament flavum during lumbar microdiscectomy, and to evaluate whether this helps prevent postoperative fibrosis and improve outcome.
    METHODS: From January to December 2017, 251 patients with indication for microdiscectomy were randomly divided into test group using ligament flavum preservation technique and control group using conventional procedures. Visual analogue scale (VAS) scores and Oswestry Disability Index (ODI) were assessed before the surgery, and 3 days, 1 month, 6 months, 1 year and 2 years after the operation respectively. The grade of epidural fibrosis on MRI after 6 months was evaluated by two radiologists independently and double-blindly.
    RESULTS: Both groups\' VAS and ODI were significantly improved after surgery, but there was no significant difference between two groups at 3d and 1 month after operation. The grade of epidural fibrosis in test group was significantly lower than that in control group at 6 months postoperative. The VAS and ODI were significantly lower in test group than that in control group at 6 months,1 year and 2 years after operation.
    CONCLUSIONS: Preservation of more ligament flavum is practicable during the procedure of microdiscectomy. It can prevent postoperative epidural fibrosis, and is helpful to achieve a better clinical outcome.
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