Experimental Rheumatology, Radboud University Medical Center, Geert Grooteplein Zuid 8, 6525 GA Nijmegen, The Netherlands.
Cells. 2023 Jul 22;12(14):1913. doi: 10.3390/cells12141913.
Joint pain severity in arthritic diseases differs between sexes and is often more pronounced in women. This disparity is thought to stem from biological mechanisms, particularly innate immunity, yet the understanding of sex-specific differences in arthritic pain remains incomplete. This study aims to investigate these disparities using an innate immunity-driven inflammation model induced by intra-articular injections of Streptococcus Cell Wall fragments to mimic both acute and pre-sensitized joint conditions. Nociceptive behavior was evaluated via gait analysis and static weight-bearing, and inflammation was evaluated via joint histology and the synovial gene expression involved in immune response. Although acute inflammation and pain severity were comparable between sexes, distinct associations between synovial inflammatory gene expression and static nociceptive behavior emerged. These associations delineated sex-specific relationships with pain, highlighting differential gene interactions ( versus on day 1 and versus on day 8) between sexes. In conclusion, our study found that, despite similar pain severity between sexes, the association of inflammatory synovial genes revealed sex-specific differences in the molecular inflammatory mechanisms underlying pain. These findings suggest a path towards more personalized treatment strategies for pain management in arthritis and other inflammatory joint diseases.
关节疼痛的严重程度在关节炎疾病中存在性别差异,且女性通常更为明显。这种差异被认为源于生物学机制,特别是先天免疫,但对关节炎疼痛的性别特异性差异的理解仍不完整。本研究旨在使用关节内注射链球菌细胞壁片段诱导的先天免疫驱动的炎症模型来研究这些差异,以模拟急性和预致敏关节状况。通过步态分析和静态负重评估伤害感受行为,通过关节组织学和参与免疫反应的滑膜基因表达评估炎症。尽管男女之间的急性炎症和疼痛严重程度相当,但滑膜炎症基因表达与静态伤害感受行为之间存在明显的关联。这些关联描绘了与疼痛的性别特异性关系,突出了性别之间的差异基因相互作用( 在第 1 天和 在第 8 天)。总之,我们的研究发现,尽管男女之间的疼痛严重程度相似,但炎症性滑膜基因的关联揭示了疼痛背后的分子炎症机制存在性别特异性差异。这些发现为关节炎和其他炎症性关节疾病的疼痛管理提供了更个性化的治疗策略的途径。