Corrado Ada, Guadagni Ilaria, Picarelli Giovanna, Variola Angela
Department of Medical and Surgical Sciences, Rheumatology Clinic, University of Foggia, Foggia, Italy.
Medical Department, Pfizer Italy, Rome, Italy.
Immun Inflamm Dis. 2025 Jan;13(1):e70080. doi: 10.1002/iid3.70080.
Immune-mediated inflammatory diseases (IMIDs) are a group of chronic conditions characterized by dysregulated immune responses and persistent inflammation. Rheumatoid arthritis (RA), spondyloarthritis (SpA), and ulcerative colitis (UC) exemplify prominent IMIDs, each presenting unique challenges for their management, that impact patient's quality of life (QoL). Obesity, marked by persistent low-grade inflammation, influences the progression, response to treatment, and clinical management of patients with RA, SpA, and UC. Besides, the emerging role of sarcopenic obesity, a special subtype of obesity with malnutrition, should be considered in the definition of the appropriated therapeutic interventions.
This narrative literature review summarizes recent evidence on the interplay between obesity-induced inflammation and IMIDs.
Obesity contributes to elevated levels of proinflammatory cytokines, influencing the inflammatory pathways common to IMIDs. White adipose tissue, acting as an endocrine organ, produces cytokines like TNF-α and IL-6, fueling chronic inflammation. The dysregulation of adipokines, such as leptin and adiponectin, further complicates this interplay, impacting immune responses and metabolic processes.
Understanding the cross-talk between inflammatory pathways in obesity and IMIDs can provide insight into potential targets for intervention. This includes lifestyle modifications aimed to regulate weight gain, paving the way for comprehensive strategies to manage IMIDs in the context of obesity.
免疫介导的炎症性疾病(IMIDs)是一组以免疫反应失调和持续性炎症为特征的慢性疾病。类风湿性关节炎(RA)、脊柱关节炎(SpA)和溃疡性结肠炎(UC)是典型的IMIDs,它们各自的管理都面临独特挑战,影响患者的生活质量(QoL)。以持续性低度炎症为特征的肥胖会影响RA、SpA和UC患者的病情进展、对治疗的反应及临床管理。此外,在确定适当的治疗干预措施时,应考虑肌少性肥胖这一伴有营养不良的肥胖特殊亚型的新作用。
本叙述性文献综述总结了关于肥胖诱导的炎症与IMIDs之间相互作用的最新证据。
肥胖导致促炎细胞因子水平升高,影响IMIDs常见的炎症途径。白色脂肪组织作为一个内分泌器官,产生如肿瘤坏死因子-α和白细胞介素-6等细胞因子,加剧慢性炎症。瘦素和脂联素等脂肪因子的失调使这种相互作用更加复杂,影响免疫反应和代谢过程。
了解肥胖和IMIDs炎症途径之间的相互作用可以为潜在的干预靶点提供见解。这包括旨在控制体重增加的生活方式改变,为在肥胖背景下管理IMIDs的综合策略铺平道路。