Graduate School of Technology, Industrial and Social Sciences, Tokushima University, Minami-Jyosanjima 1-1, Tokushima, 770-8502, Japan.
Department of Orthopaedic Surgery, National Hospital Organization Kochi National Hospital, Kochi, Japan.
BMC Musculoskelet Disord. 2022 Aug 25;23(1):811. doi: 10.1186/s12891-022-05762-3.
Severe frozen shoulder (FS) is often resistant to treatment and can thus result in long-term functional impairment. However, its etiology remains unknown. We hypothesized that gene expression of FS would vary by synovial location.
The synovial tissues of patients with FS were collected prospectively and analyzed for the expression of 19 genes. Synovial tissues from patients with rotator cuff tear (RCT) or shoulder instability (SI) were also analyzed as controls. A total of 10 samples were analyzed from each group. The specimens were arthroscopically taken from three different locations: rotator interval (RI), axillary recess (AX), and subacromial bursa (SAB). Total RNA was extracted from the collected tissues and was analyzed by real-time polymerase chain reaction for the following genes: matrix metalloproteinases (MMPs); tissue inhibitors of metalloproteinases (TIMPs); inflammatory cytokines (IL1B, TNF, and IL6); type I and II procollagen (COL1A1 and COL2A1); growth factors (IGF1 and TGFB1); neural factors (NGF and NGFR); SOX9; and ACTA2.
Site-specific analysis showed that MMP13, IL-6, SOX9, and COL1A1 were increased in all three sites. Four genes (MMP3, MMP9, COL2A1, and NGFR) were increased in the AX, MMP3 in the RI, and NGFR in the SAB were increased in the FS group than in the RCT and SI groups. In the FS group, there was a correlation between the expression of genes related to chondrogenesis (MMP2, IGF1, SOX9, COL2A1, NGF, and NGFR) or fibrosis (MMP9, TGFB1, and COL1A1).
The expression levels of numerous MMPs, pro-inflammatory cytokines, and collagen-related genes were increased in the FS group, suggesting that catabolic and anabolic changes have simultaneously occurred. In addition, genes related to chondrogenesis or fibrosis were highly expressed in the FS group, which might have affected the range of motion limitation of the shoulder. Compared to RI and SAB, the AX was the most common site of increased expression in FS. Analyzing the lower region of the shoulder joint may lead to the elucidation of the pathogenesis of FS.
重度冻结肩(FS)通常对治疗有抗性,因此会导致长期的功能障碍。然而,其病因仍然未知。我们假设 FS 的滑膜组织基因表达会因滑膜位置而异。
前瞻性收集 FS 患者的滑膜组织并分析 19 个基因的表达情况。同时还分析了肩袖撕裂(RCT)或肩不稳(SI)患者的滑膜组织作为对照。每组分析了 10 个样本。关节镜下从三个不同部位(肩袖间隙 RI、腋窝 AX 和肩峰下囊 SAB)采集标本。从收集的组织中提取总 RNA,通过实时聚合酶链反应分析以下基因:基质金属蛋白酶(MMPs);金属蛋白酶组织抑制剂(TIMPs);炎症细胞因子(IL1B、TNF 和 IL6);I 型和 II 型前胶原(COL1A1 和 COL2A1);生长因子(IGF1 和 TGFB1);神经因子(NGF 和 NGFR);SOX9;和 ACTA2。
部位特异性分析显示,MMP13、IL-6、SOX9 和 COL1A1 在所有三个部位均增加。四个基因(MMP3、MMP9、COL2A1 和 NGFR)在 AX 增加,MMP3 在 RI 增加,NGFR 在 SAB 增加,FS 组比 RCT 和 SI 组增加。在 FS 组中,与软骨生成(MMP2、IGF1、SOX9、COL2A1、NGF 和 NGFR)或纤维化(MMP9、TGFB1 和 COL1A1)相关的基因表达之间存在相关性。
FS 组中许多 MMPs、促炎细胞因子和胶原相关基因的表达水平增加,提示同时发生了分解代谢和合成代谢变化。此外,FS 组中与软骨生成或纤维化相关的基因高度表达,这可能影响了肩部的活动范围受限。与 RI 和 SAB 相比,AX 是 FS 中最常见的高表达部位。分析肩关节的下部区域可能有助于阐明 FS 的发病机制。