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肥胖对炎症性肠病患者生物治疗反应的影响。

Impact of Obesity on Response to Biologic Therapies in Patients with Inflammatory Bowel Diseases.

机构信息

Department of Medicine, Rutgers Biomedical and Health Sciences, Newark, NJ, USA.

Division of Gastroenterology, Department of Medicine, University of California San Diego, ACTRI 1W501, 9452 Medical Center Dr., La Jolla, CA, 92093, USA.

出版信息

BioDrugs. 2022 Mar;36(2):197-203. doi: 10.1007/s40259-022-00522-0. Epub 2022 Mar 23.

Abstract

Approximately 20-40% of patients with inflammatory bowel disease (IBD) are obese. Obesity is associated with inferior outcomes in patients with IBD, with lower rates of achieving remission, poor quality of life, and higher burden of unplanned healthcare utilization. Multiple cohort studies in patients with immune-mediated inflammatory diseases, including IBD, treated with biologic agents like tumor necrosis factor-α antagonists have suggested that obesity is associated with inferior response to biologic therapy. This may be related to the negative impact of obesity on the pharmacokinetics of biologic agents. Pharmacokinetic studies of multiple biologic agents have demonstrated that high body weight is associated with more rapid clearance and a higher volume of distribution of biologic agents, which leads to low trough concentrations. Randomized trials in patients with psoriasis and psoriatic arthritis treated with biologic agents suggest that diet- or lifestyle-induced weight loss is associated with improved response to therapy. This provides an opportunity to explore intentional weight loss as adjunctive therapy in obese patients with IBD. However, diet and lifestyle interventions for weight loss are hard to implement in patients with IBD; hence, long-term therapy with weight-loss agents (such as with phentermine-topiramate, naltrexone-bupropion) is attractive as adjunctive therapy in obese patients with IBD.

摘要

大约 20-40% 的炎症性肠病 (IBD) 患者肥胖。肥胖与 IBD 患者的不良结局相关,这些患者缓解率较低、生活质量较差、非计划性医疗保健利用率较高。包括 IBD 在内的免疫介导的炎症性疾病患者的多项队列研究表明,肥胖与生物治疗反应不佳相关。这可能与肥胖对生物制剂药代动力学的负面影响有关。多项生物制剂的药代动力学研究表明,体重较高与生物制剂的清除率加快和分布容积更高相关,这会导致药物浓度低谷降低。接受生物制剂治疗的银屑病和银屑病关节炎患者的随机试验表明,饮食或生活方式引起的体重减轻与治疗反应的改善相关。这为肥胖的 IBD 患者探索将体重减轻作为辅助治疗提供了机会。然而,饮食和生活方式干预措施对于减轻体重来说很难在 IBD 患者中实施;因此,对于肥胖的 IBD 患者,长期使用减肥药物(如安非他酮-纳曲酮、苯丁胺-托吡酯)作为辅助治疗具有吸引力。

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