Association of denosumab with serum cytokines, chemokines, and bone-related factors in patients with rheumatoid arthritis: A post hoc analysis of a multicentre, open-label, randomised, parallel-group study.

IF 1.8 4区 医学 Q3 RHEUMATOLOGY
Naoki Iwamoto, Shuntaro Sato, Kaori Furukawa, Toru Michitsuji, Kazuteru Shiraishi, Kounosuke Watanabe, Ko Chiba, Makoto Osaki, Atsushi Kawakami
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Abstract

Objectives: To clarify changes in serum cytokines, chemokines, and bone-related factors during denosumab treatment in rheumatoid arthritis (RA) patients.

Methods: This was a post hoc analysis of a multicentre, open-label, randomised, parallel-group study. Patients were randomly assigned to continue treatment with conventional synthetic disease-modifying anti-rheumatic drugs (csDMARDs) plus receive treatment with denosumab (csDMARDs plus denosumab group) or to continue treatment with csDMARD therapy alone for 12 months. Serum biomarker levels were measured at baseline and at 6 and 12 months.

Results: Baseline and 6-month data from the csDMARDs plus denosumab (n = 22) and csDMARD therapy alone (n = 22) groups were analysed. Statistically significant changes from baseline were seen: Dickkopf-related protein 1 decreased at 6 and 12 months (both groups); osteopontin decreased at 6 months in the csDMARDs plus denosumab group; osteopontin and soluble CD40 ligand increased at 6 and 12 months in the csDMARD therapy alone group; osteocalcin decreased at 6 and 12 months, epidermal growth factor decreased at 12 months, and macrophage-derived chemokine decreased at 6 months in the csDMARDs plus denosumab group; and interferon gamma-induced protein-10 increased at 12 months in the csDMARD therapy alone group.

Conclusions: Denosumab may inhibit bone destruction by suppressing bone-related factors/chemokines.

地诺单抗与类风湿性关节炎患者血清细胞因子、趋化因子和骨相关因子的关系:一项多中心、开放标签、随机、平行组研究的事后分析。
目的:明确类风湿关节炎(RA)患者在接受地诺单抗治疗期间血清细胞因子、趋化因子和骨相关因子的变化:明确类风湿性关节炎(RA)患者在接受地诺单抗治疗期间血清细胞因子、趋化因子和骨相关因子的变化:这是一项多中心、开放标签、随机、平行组研究的事后分析。患者被随机分配到继续接受传统合成改善病情抗风湿药(csDMARDs)治疗并接受地诺单抗治疗(csDMARDs加地诺单抗组),或继续接受为期12个月的单纯csDMARD治疗。在基线、6个月和12个月时测量血清生物标志物水平:对csDMARDs加denosumab组(22人)和单纯csDMARD治疗组(22人)的基线和6个月数据进行了分析。与基线相比,两组数据均出现了统计学意义上的重大变化:在 6 个月和 12 个月时(两组),与 dickkopf 相关的蛋白 1 均有所下降;在 csDMARDs+Denosumab 组中,6 个月时骨桥蛋白有所下降;在单独使用 csDMARD 治疗组中,6 个月和 12 个月时骨桥蛋白和可溶性 CD40 配体均有所上升;骨钙素在6个月和12个月时减少,表皮生长因子在12个月时减少,巨噬细胞衍生趋化因子在6个月时减少;干扰素γ诱导蛋白-10在12个月时增加。结论地诺单抗可通过抑制骨相关因子/趋化因子来抑制骨破坏。
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来源期刊
Modern Rheumatology
Modern Rheumatology RHEUMATOLOGY-
CiteScore
4.90
自引率
9.10%
发文量
146
审稿时长
1.5 months
期刊介绍: Modern Rheumatology publishes original papers in English on research pertinent to rheumatology and associated areas such as pathology, physiology, clinical immunology, microbiology, biochemistry, experimental animal models, pharmacology, and orthopedic surgery. Occasional reviews of topics which may be of wide interest to the readership will be accepted. In addition, concise papers of special scientific importance that represent definitive and original studies will be considered. Modern Rheumatology is currently indexed in Science Citation Index Expanded (SciSearch), Journal Citation Reports/Science Edition, PubMed/Medline, SCOPUS, EMBASE, Chemical Abstracts Service (CAS), Google Scholar, EBSCO, CSA, Academic OneFile, Current Abstracts, Elsevier Biobase, Gale, Health Reference Center Academic, OCLC, SCImago, Summon by Serial Solutions
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