Chengdu medical college, No. 783 XinDu Road, Chengdu, 610500 Sichuan Province, PR China.
West China Hospital, Sichuan University, Chengdu, 610041 Sichuan Province, PR China.
Joint Bone Spine. 2019 Mar;86(2):173-183. doi: 10.1016/j.jbspin.2018.03.007. Epub 2018 Apr 7.
Obesity is a worldwide epidemic and a growing body of evidence suggests that it may affect the body's response to biologic agents. We investigated the influence of obesity on the efficacy of different biologic agents used to treat inflammatory diseases.
Medline, EMBASE and the Cochrane Database were searched using relevant MeSH and keyword terms for obesity and bDMARDs. Articles were selected if they reported a clinical response in obese subjects relative to other BMI categories. Response and remission outcomes were assessed using meta-analysis and all other reported outcomes were summarized.
Among the 3850 records retrieved, 24 articles met the inclusion criteria, including 10 on rheumatoid arthritis (RA), 4 on axial spondyloarthritis (axSpA), 4 on Crohn's disease (CD), 4 on psoriasis (Ps) and 2 on psoriasic arthritis (PsA). Four biological disease-modifying anti-rheumatic drugs (bDMARDs) - anti-TNF agents, T cell co-stimulation inhibitor (abatacept), IL-6 inhibitor (tocilizumab), and B-cell depletion therapy (rituximab) - were involved. The meta-analysis showed that the odds to reach a good response or achieve remission were lower in obese (BMI>30kg/m) than non-obese (BMI≤30kg/m) patients who were treated with anti-TNF agents (good responder % in RA: OR 0.34, 95% CI 0.18-0.64; remission% in RA: OR 0.36, 95% CI 0.21-0.59; BASDAI50% in axSpA: OR 0.41, 95% CI 0.21-0.83), but no significant difference between obese and non-obese was found in patients treated with abatacept (good responder % in RA: OR 0.75, 95% CI 0.42-1.36; remission% in RA: OR 0.84, 95% CI 0.65-1.09) and tocilizumab (good responder % in RA: OR 1.08, 95% CI 0.44-2.63; remission% in RA: OR 0.91, 95% CI 0.50-1.66).
Obesity hampered the effect of anti-TNF agents, but not those of abatacept and tocilizumab, suggesting that a personalized treatment strategy should be considered for obese patients with inflammatory diseases.
肥胖是一种全球性的流行疾病,越来越多的证据表明,它可能会影响人体对生物制剂的反应。我们研究了肥胖对用于治疗炎症性疾病的不同生物制剂疗效的影响。
使用肥胖和生物 DMARDs 的相关 MeSH 和关键词在 Medline、EMBASE 和 Cochrane 数据库中进行检索。如果报告了肥胖受试者相对于其他 BMI 类别在临床反应方面的研究,则选择这些文章。使用荟萃分析评估反应和缓解结果,总结所有其他报告的结果。
在检索到的 3850 条记录中,有 24 篇文章符合纳入标准,其中 10 篇关于类风湿关节炎(RA),4 篇关于中轴型脊柱关节炎(axSpA),4 篇关于克罗恩病(CD),4 篇关于银屑病(Ps)和 2 篇关于银屑病关节炎(PsA)。涉及 4 种生物疾病修饰抗风湿药物(bDMARDs)-抗 TNF 制剂、T 细胞共刺激抑制剂(阿巴西普)、IL-6 抑制剂(托珠单抗)和 B 细胞耗竭治疗(利妥昔单抗)。荟萃分析表明,与非肥胖(BMI≤30kg/m)患者相比,接受抗 TNF 制剂治疗的肥胖(BMI>30kg/m)患者达到良好反应或缓解的几率较低(RA 中的良好反应%:OR 0.34,95%CI 0.18-0.64;RA 中的缓解%:OR 0.36,95%CI 0.21-0.59;axSpA 中的 BASDAI50%:OR 0.41,95%CI 0.21-0.83),但在接受阿巴西普治疗的患者中,肥胖与非肥胖之间无显著差异(RA 中的良好反应%:OR 0.75,95%CI 0.42-1.36;RA 中的缓解%:OR 0.84,95%CI 0.65-1.09)和托珠单抗(RA 中的良好反应%:OR 1.08,95%CI 0.44-2.63;RA 中的缓解%:OR 0.91,95%CI 0.50-1.66)。
肥胖阻碍了抗 TNF 制剂的疗效,但不影响阿巴西普和托珠单抗的疗效,这表明对于患有炎症性疾病的肥胖患者,应考虑采用个性化治疗策略。