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RMD Open. 2017 Aug 9;3(2):e000458. doi: 10.1136/rmdopen-2017-000458. eCollection 2017.
2
Body mass index and clinical response to intravenous or subcutaneous abatacept in patients with rheumatoid arthritis.体重指数与静脉或皮下注射阿巴西普治疗类风湿关节炎患者的临床应答。
Clin Rheumatol. 2017 Dec;36(12):2655-2665. doi: 10.1007/s10067-017-3788-1. Epub 2017 Aug 18.
3
Pathogenetic insights from the treatment of rheumatoid arthritis.从类风湿关节炎治疗中获得的发病机制见解。
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Ann Rheum Dis. 2017 Jun;76(6):960-977. doi: 10.1136/annrheumdis-2016-210715. Epub 2017 Mar 6.
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The effect of body mass index on clinical response to abatacept as a first-line biologic for rheumatoid arthritis: 6-month results from the 2-year, observational, prospective ACTION study.体重指数对依那西普作为类风湿关节炎一线生物制剂的临床应答的影响:来自为期 2 年、观察性、前瞻性 ACTION 研究的 6 个月结果。
Joint Bone Spine. 2017 Oct;84(5):571-576. doi: 10.1016/j.jbspin.2016.10.011. Epub 2016 Dec 30.
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Body mass does not impact the clinical response to intravenous abatacept in patients with rheumatoid arthritis. Analysis from the "pan-European registry collaboration for abatacept (PANABA).体重并不影响类风湿关节炎患者对静脉注射阿巴西普的临床反应。来自“阿巴西普全欧洲注册协作组(PANABA)”的分析。
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Towards a multidisciplinary approach to understand and manage obesity and related diseases.迈向采用多学科方法理解和管理肥胖症及相关疾病。
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Body mass index and response to abatacept in rheumatoid arthritis.体重指数与类风湿关节炎中阿巴西普的应答反应。
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Rheumatoid arthritis.类风湿关节炎
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Clin Rheumatol. 2016 May;35(5):1129-36. doi: 10.1007/s10067-016-3220-2. Epub 2016 Mar 1.

类风湿关节炎患者的体重指数与托珠单抗的临床反应

Body Mass Index and Clinical Response to Tocilizumab in Patients With Rheumatoid Arthritis.

作者信息

Huang Hua, Cen Han, Zhou Li, Wang Ting-Hui, Qin Wen, Xie Bin-Hua, Xiao Dong-Mei, Wu Xiu-Di, Wu Hua-Xiang

机构信息

Department of Rheumatology, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.

Department of Preventive Medicine, Medical School of Ningbo University, Ningbo, China.

出版信息

Arch Rheumatol. 2019 Apr 22;34(4):406-413. doi: 10.5606/ArchRheumatol.2019.7146. eCollection 2019 Dec.

DOI:10.5606/ArchRheumatol.2019.7146
PMID:32010889
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6974388/
Abstract

OBJECTIVES

This study aims to determine whether baseline body mass index (BMI) affects clinical response to tocilizumab (TCZ) after six months of treatment in rheumatoid arthritis (RA) patients.

PATIENTS AND METHODS

In this prospective study, a total of 52 RA patients (10 males, 42 females; mean age 50.6±12.2 years; range, 23 to 73 years) receiving intravenous TCZ were consecutively recruited and followed-up for six months. BMI was calculated before initiation of TCZ treatment. The primary clinical response criterion was clinical disease activity index (CDAI) low disease activity (LDA) and the secondary clinical response criteria included CDAI remission, disease activity score based on 28 joints (DAS28)-erythrocyte sedimentation rate (ESR) LDA, DAS28-ESR remission, European League Against Rheumatism (EULAR) good response, and decreased DAS28-ESR (ΔDAS28-ESR)≥1.2.

RESULTS

The number of RA patients classified as normal weight, overweight, and obese according to baseline BMI was 38 (73.1%), eight (15.4%), and six (11.5%), respectively. Similar baseline BMI median levels were found between RA patients reaching CDAI LDA and non-LDA: 21.11 (18.94-23.72) versus 20.78 (20.03-22.29) (p=0.98), and non-significant difference in the proportion of responders between normal weight and overweight/obese RA patients was found (p=0.47). No significant difference was found when the secondary clinical response criteria were applied.

CONCLUSION

Our study demonstrates that BMI is not associated with clinical response to TCZ among RA patients and TCZ may be used to treat RA patients regardless of BMI levels.

摘要

目的

本研究旨在确定类风湿关节炎(RA)患者在接受托珠单抗(TCZ)治疗6个月后,基线体重指数(BMI)是否会影响临床反应。

患者与方法

在这项前瞻性研究中,连续招募了52例接受静脉注射TCZ的RA患者(10例男性,42例女性;平均年龄50.6±12.2岁;范围为23至73岁),并进行了6个月的随访。在开始TCZ治疗前计算BMI。主要临床反应标准为临床疾病活动指数(CDAI)低疾病活动度(LDA),次要临床反应标准包括CDAI缓解、基于28个关节的疾病活动评分(DAS28)-红细胞沉降率(ESR)LDA、DAS28-ESR缓解、欧洲抗风湿病联盟(EULAR)良好反应以及DAS28-ESR降低(ΔDAS28-ESR)≥1.2。

结果

根据基线BMI分类,体重正常、超重和肥胖的RA患者数量分别为38例(73.1%)、8例(15.4%)和6例(11.5%)。达到CDAI LDA和未达到CDAI LDA的RA患者之间的基线BMI中位数水平相似:21.11(18.94 - 23.72)与20.78(20.03 - 22.29)(p = 0.98),并且体重正常与超重/肥胖的RA患者之间的反应者比例无显著差异(p = 0.47)。应用次要临床反应标准时未发现显著差异。

结论

我们的研究表明,RA患者中BMI与对TCZ的临床反应无关,无论BMI水平如何,TCZ均可用于治疗RA患者。