Toussirot Eric
INSERM CIC-1431, CHU de Besançon, Centre d'Investigation Clinique Biothérapie, Pôle Recherche, 25000 Besançon, France.
Fédération Hospitalo-Universitaire INCREASE, CHU de Besançon, 25000 Besançon, France.
Metabolites. 2020 Mar 13;10(3):107. doi: 10.3390/metabo10030107.
Obesity is a comorbidity that plays a role in the development and severity of inflammatory joint diseases, including rheumatoid arthritis, psoriatic arthritis and axial spondyloarthritis. The relationships between obesity and adipose tissue and the treatments given for inflammatory joint diseases are bidirectional. In fact, biological agents (bDMARDs) and targeted synthetic agents (tsDMARDs) may influence body weight and body composition of treated patients, while obesity in turn may influence clinical response to these agents. Obesity is a prevalent comorbidity mainly affecting patients with rheumatoid arthritis (RA) and psoriatic arthritis (PsA) with specific phenotypes. Tumour necrosis factor alpha (TNFα) inhibitors have been associated with changes in body composition by improving lean mass, but also by significantly increasing fat mass, which localized toward the abdominal/visceral region. The IL-6 inhibitor tocilizumab is associated with an increase in lean mass without change in fat mass. The clinical response to TNFα inhibitors is attenuated by obesity, an effect that is less pronounced with IL-6 inhibitors and the B-cell depletion agent rituximab. Conversely, body weight has no influence on the response to the costimulation inhibitor abatacept. These effects may be of help to the physician in personalized medicine, and may guide the therapeutic choice in obese/overweight patients.
肥胖是一种合并症,在包括类风湿性关节炎、银屑病关节炎和轴性脊柱关节炎在内的炎症性关节疾病的发生和严重程度中起作用。肥胖与脂肪组织以及针对炎症性关节疾病的治疗之间的关系是双向的。事实上,生物制剂(bDMARDs)和靶向合成制剂(tsDMARDs)可能会影响接受治疗患者的体重和身体组成,而肥胖反过来可能会影响对这些制剂的临床反应。肥胖是一种普遍的合并症,主要影响具有特定表型的类风湿性关节炎(RA)和银屑病关节炎(PsA)患者。肿瘤坏死因子α(TNFα)抑制剂与身体组成的变化有关,这是通过改善瘦体重实现的,但也通过显著增加脂肪量来实现,脂肪量主要集中在腹部/内脏区域。白细胞介素-6抑制剂托珠单抗与瘦体重增加有关,而脂肪量没有变化。肥胖会减弱对TNFα抑制剂的临床反应,这种影响在白细胞介素-6抑制剂和B细胞清除剂利妥昔单抗中不太明显。相反,体重对共刺激抑制剂阿巴西普的反应没有影响。这些影响可能有助于医生进行个性化医疗,并指导肥胖/超重患者的治疗选择。