UOC di Neurochirurgia, Azienda Ospedaliera Sant'Andrea, Sapienza, Roma, Italy.
UOC di Ortopedia e Traumatologia, Università degli studi di Perugia, Perugia, Italy.
Eur Spine J. 2020 Jun;29(6):1410-1415. doi: 10.1007/s00586-020-06412-9. Epub 2020 Apr 16.
Degenerative disc disease (DDD) is a common condition causing low-back pain, disability and, eventually, neurological symptoms. This investigation aimed to investigate intervertebral disc DDD-related changes, evaluating histomorphology and cytokines secretion, and their clinical-radiological correlations.
This is a monocentric prospective observational study. A cohort of patients who underwent microdiscectomy for DDD, from June 2018 to January 2019, were enrolled. Discs samples were examined for histomorphology, chondrons count, immunohistochemistry for Hif-1α, Nf200 and Egr-1. Demographical and clinical data were also collected.
Twenty patients were finally included. MRI evaluation showed a Modic I alteration in nine patients and a Modic II in 11. The disability grade was low-moderate (ODI score was ≤ 40%) in eight patients and high (ODI score > 40%) in 12. The Modic I was associated with a low-moderate disability in two (22%) patients and to a high disability in seven (88%) (p < 0.01). In Modic I group and in ODI > 40% groups, there were a significative higher mean disability grade 48.4 (± 8.3)%, number of chondrons per section, cells per chondron, Nf200+ nerve fibers and Hif-1α expression, compared with Modic II and ODI ≤ 40% groups, respectively. There were no differences in terms of Egr-1 expression.
The discs with Modic I MRI signal could represent potential targets for medical treatments, whereas Modic II seems to be a more likely point of no return in a degenerative process. Therefore, further investigations are to better investigate inflammatory pathways and degenerative mechanisms in DDD.
退行性椎间盘疾病(DDD)是一种常见的引起下腰痛、残疾并最终导致神经症状的疾病。本研究旨在探讨与椎间盘退行性改变相关的变化,评估组织形态学和细胞因子分泌及其与临床影像学的相关性。
这是一项单中心前瞻性观察研究。我们纳入了 2018 年 6 月至 2019 年 1 月期间因 DDD 接受微创手术的患者队列。对椎间盘样本进行组织形态学、软骨细胞计数、缺氧诱导因子-1α(Hif-1α)、神经丝 200(Nf200)和早期生长反应因子-1(Egr-1)免疫组化染色检查。同时收集人口统计学和临床数据。
最终共有 20 例患者纳入本研究。MRI 评估显示 9 例患者存在 Modic I 改变,11 例患者存在 Modic II 改变。8 例患者的残疾程度为低中度(ODI 评分≤40%),12 例患者为高度(ODI 评分>40%)。Modic I 与 2 例(22%)患者的低中度残疾和 7 例(88%)患者的高度残疾相关(p<0.01)。在 Modic I 组和 ODI>40%组中,每个软骨细胞的软骨细胞数量、每个软骨细胞的细胞数量、Nf200+神经纤维和 Hif-1α表达均显著高于 Modic II 组和 ODI≤40%组,而 Egr-1 表达则无差异。
MRI 信号呈 Modic I 的椎间盘可能是药物治疗的潜在靶点,而 Modic II 似乎是退行性过程中不可逆转的一个点。因此,需要进一步研究来更好地探讨 DDD 中的炎症途径和退行性机制。