Neuropeptide-Mediated Crosstalk between Subchondral Bone and Articular Cartilage in Ankle Osteoarthritis: A Cross-Sectional Histologic Study of 17 Ankles.

IF 2.2
Saori Ishibashi, Tomoyuki Nakasa, Yasunari Ikuta, Satoru Sakurai, Dan Moriwaki, Taro Chujo, Nobuo Adachi
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Abstract

Background: This study aimed to investigate the expression patterns of the neuropeptides, calcitonin gene-related peptide (CGRP), and substance P (SP), in the subchondral bone of patients with ankle osteoarthritis (OA) and examine their association with subchondral bone changes and cartilage degeneration. We hypothesized that neuropeptides were expressed in sclerotic subchondral bone and that this expression was associated with the progression of cartilage degeneration. This study investigated neuropeptide expression and its relationship with subchondral bone changes and cartilage degeneration in ankle OA.

Methods: Seventeen ankles of 16 patients who underwent total ankle arthroplasty for ankle OA were analyzed. Radiographic, histologic, and CT evaluations were conducted, including the measurement of Hounsfield unit (HU) values, subchondral bone plate thickness, trabecular bone area, and modified Mankin scores. Immunohistochemistry for CGRP; SP; collagen types I, II, and X; and TRAP staining for osteoclasts were performed.

Results: Subchondral bone sclerosis and cartilage degeneration progressed concurrently with increased thickness and trabecular area beneath the degenerated cartilage. CGRP and SP expression were significantly upregulated in the sclerotic subchondral bone, showing strong positive correlations with HU values, subchondral bone thickness, and Mankin scores. CGRP expression appeared earlier than SP expression in moderate degeneration stages. The number of TRAP-positive osteoclasts increased with degeneration and followed a distribution pattern similar to that of CGRP and SP.

Conclusion: CGRP and SP expression in the subchondral bone was closely linked to structural bone changes and cartilage degradation in ankle OA. Their early expression and association with osteoclast activity support a potential role in OA pathogenesis; however, causation cannot be inferred from this cross-sectional study.

踝关节骨性关节炎中软骨下骨和关节软骨间神经肽介导的串扰:17个踝关节的横断面组织学研究。
背景:本研究旨在探讨降钙素基因相关肽(CGRP)和P物质(SP)在踝关节骨关节炎(OA)患者软骨下骨中的表达模式,并探讨其与软骨下骨变化和软骨退变的关系。我们假设神经肽在硬化软骨下骨中表达,并且这种表达与软骨退变的进展有关。本研究探讨了踝关节骨性关节炎中神经肽的表达及其与软骨下骨变化和软骨退变的关系。方法:对16例全踝关节置换术治疗踝关节骨性关节炎患者的17只踝关节进行分析。进行影像学、组织学和CT评估,包括测量Hounsfield单位(HU)值、软骨下钢板厚度、骨小梁面积和修正的Mankin评分。CGRP免疫组化;SP;I、II、X型胶原蛋白;进行破骨细胞TRAP染色。结果:软骨下骨硬化和软骨退变同时发生,退变软骨下的软骨厚度和小梁面积增加。CGRP和SP在硬化软骨下骨中的表达显著上调,与HU值、软骨下骨厚度、Mankin评分呈强正相关。在中度退行性变阶段,CGRP表达早于SP表达。trap阳性破骨细胞数量随骨性变性而增加,其分布规律与CGRP和SP相似。结论:CGRP和SP在软骨下骨中的表达与踝关节骨性关节炎的骨结构改变和软骨退化密切相关。它们的早期表达和与破骨细胞活性的关联支持OA发病机制的潜在作用;然而,不能从这个横断面研究中推断出因果关系。
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