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血清 CCL5 水平升高与女性颞下颌关节退行性关节病的病理生理学的关系。

Association between an Increased Serum CCL5 Level and Pathophysiology of Degenerative Joint Disease in the Temporomandibular Joint in Females.

机构信息

Department of Oral Diagnosis and Medicine, Faculty and Graduate School of Dental Medicine, Hokkaido University, Sapporo 060-8586, Japan.

Department of Pharmacology, Faculty and Graduate School of Dental Medicine, Hokkaido University, Sapporo 060-8686, Japan.

出版信息

Int J Mol Sci. 2023 Feb 1;24(3):2775. doi: 10.3390/ijms24032775.

DOI:10.3390/ijms24032775
PMID:36769097
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9917489/
Abstract

Degenerative joint disease of the temporomandibular joints (DJD-TMJ) clinically manifests with symptoms such as orofacial pain, joint sounds and limited jaw movements. Our research group previously reported the functional necessity of a chemokine-chemokine receptor axis of CCL5-CCR5 in osteoclasts. Accumulated studies reported that this axis was involved in the pathogenesis of bone and joint destructive diseases, suggesting CCL5 as a potent biomarker. This study investigated whether or not the serum level of CCL5 can be a biomarker of DJD-TMJ and concomitantly analyzed changes in the serum and urine levels of bone markers to see whether or not changes in the rate of bone metabolism were predisposing. We enrolled 17 female subjects with diagnosed DJD-TMJ and sexually and age-matched 17 controls. The serum CCL5 level in DJD-TMJ subjects was significantly higher than that in the control subjects. Multivariate analyses indicated an association between an augmented CCL5 level and the rate of bone metabolism, especially in relatively young DJD-TMJ subjects without other systemic symptoms. A principal component analysis of serum markers and our pharmacological experiment using a postmenopausal model of ovariectomized rats suggested that an augmented serum CCL5 level specifically reflected DJD-TMJ and that covert changes in the rate of bone metabolism predisposed individuals to DJD-TMJ.

摘要

颞下颌关节退行性疾病(DJD-TMJ)临床上表现为口面疼痛、关节弹响和下颌运动受限等症状。我们的研究小组之前报道了趋化因子-趋化因子受体轴 CCL5-CCR5 在破骨细胞中的功能必要性。积累的研究报告表明,该轴参与了骨和关节破坏性疾病的发病机制,提示 CCL5 作为一种潜在的生物标志物。本研究旨在探讨血清 CCL5 水平是否可作为 DJD-TMJ 的生物标志物,并同时分析骨标志物的血清和尿液水平的变化,以观察骨代谢率的变化是否具有倾向性。我们招募了 17 名女性 DJD-TMJ 患者和 17 名年龄和性别匹配的对照者。DJD-TMJ 患者的血清 CCL5 水平明显高于对照组。多变量分析表明,CCL5 水平升高与骨代谢率之间存在关联,尤其是在没有其他全身症状的相对年轻的 DJD-TMJ 患者中。对血清标志物的主成分分析以及我们使用绝经后去卵巢大鼠模型的药理学实验表明,血清 CCL5 水平升高可特异性反映 DJD-TMJ,而骨代谢率的隐匿性变化可使个体易患 DJD-TMJ。

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