Molecular and Cellular Gastroenterology, Health Research Institute of Santiago de Compostela (IDIS), Santiago de Compostela, Spain.
SERGAS (Health Service from Galicia) and IDIS (Health Research Institute of Santiago de Compostela), The NEIRID Lab (Neuroendocrine Interactions in Rheumatology and Inflammatory Diseases), Research Laboratory 9, Santiago University Clinical Hospital, Santiago de Compostela, Spain.
Mediators Inflamm. 2024 Oct 7;2024:7264704. doi: 10.1155/2024/7264704. eCollection 2024.
Obesity is associated with an increased risk for different chronic diseases such as osteoarthritis (OA) or rheumatoid arthritis (RA). In fact, adipose tissue is now recognized as an endocrine organ able to secrete a wide variety of factors called adipokines, which have been demonstrated to participate in the pathophysiology of RA by regulating inflammation and immunity. LCN2 is one of these adipose tissue-derived factors. However, scarce information is available about the levels of this adipokine in different rheumatic diseases. Therefore, we aimed to analyze LCN2 serum levels in healthy, OA, and RA patients under different treatments.
Serum levels of LCN2, among other proinflammatory and chemotactic factors, have been measured by ELISA or Multiplex in the following four groups of individuals: healthy, OA, and RA patients treated with conventional treatment or adalimumab.
We found increased serum levels of LCN2 in OA and RA patients. Interestingly, LCN2 serum levels show a similar pattern to that observed for different proinflammatory and chemotactic factors, being increased in RA conventional treated patients in comparison to RA patients treated with adalimumab. Also, RA patients under conventional treatment revealed a positive and significant correlation between LCN2 and CCL2, CCL3, IL-8, IL-1, IL-6, and CRP. In patients with RA treated with adalimumab, only IL-6 and CRP correlated significantly with LCN2.
Our results clearly suggest that LCN2 is modulated and associated with inflammation in rheumatic diseases. Therefore, the serum levels of this adipokine might be used as an additional biomarker of the inflammatory/disease activity.
肥胖与多种慢性疾病(如骨关节炎[OA]或类风湿关节炎[RA])的风险增加有关。事实上,脂肪组织现在被认为是一种能够分泌多种被称为脂肪因子的内分泌器官,这些因子通过调节炎症和免疫参与 RA 的病理生理学。LCN2 就是这些脂肪组织来源的因子之一。然而,关于这种脂肪因子在不同风湿性疾病中的水平,信息仍然有限。因此,我们旨在分析健康人群、OA 和 RA 患者在不同治疗下的 LCN2 血清水平。
通过 ELISA 或 Multiplex 测量了 LCN2 等促炎和趋化因子在以下四组个体中的血清水平:健康人群、OA 和接受常规治疗或阿达木单抗治疗的 RA 患者。
我们发现 OA 和 RA 患者的血清 LCN2 水平升高。有趣的是,LCN2 血清水平呈现出与观察到的不同促炎和趋化因子相似的模式,与接受阿达木单抗治疗的 RA 患者相比,接受常规治疗的 RA 患者的 LCN2 血清水平升高。此外,接受常规治疗的 RA 患者的 LCN2 与 CCL2、CCL3、IL-8、IL-1、IL-6 和 CRP 之间呈正相关且具有统计学意义。在接受阿达木单抗治疗的 RA 患者中,只有 IL-6 和 CRP 与 LCN2 显著相关。
我们的结果清楚地表明,LCN2 在风湿性疾病中受到调节并与炎症相关。因此,这种脂肪因子的血清水平可能被用作炎症/疾病活动的额外生物标志物。