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阿那白滞素对比肿瘤坏死因子抑制剂治疗类风湿关节炎和 2 型糖尿病的获益:来自 TRACK 研究的长期随访结果,该研究是一项多中心、开放性标签、随机、对照试验。

Benefits of anakinra versus TNF inhibitors in rheumatoid arthritis and type 2 diabetes: long-term findings from participants furtherly followed-up in the TRACK study, a multicentre, open-label, randomised, controlled trial.

机构信息

Rheumatology, Department of Biotechnological and Applied Clinical Sciences, University of L'Aquila, Italy.

Rheumatology and Immunology Unit, Department of Medicine, University of Rome 'Campus Biomedico', Rome, Italy.

出版信息

Clin Exp Rheumatol. 2021 Mar-Apr;39(2):403-406. doi: 10.55563/clinexprheumatol/phsqg7. Epub 2021 Mar 3.

Abstract

OBJECTIVES

Interleukin (IL)-1β is considered a shared pathogenic mediator between rheumatoid arthritis (RA) and type 2 diabetes (T2D). In the TRACK study, participants with both diseases were randomised to an IL-1 inhibitor, anakinra, or a TNF inhibitor (TNFi). After 6 months, anakinra induced a such of improvement on metabolic and inflammatory parameters, leading to a premature stoppage of the study. Thus, we aimed to assess how long IL-1 inhibition benefits lasted.

METHODS

Since the TRACK was prematurely discontinued for "early benefit", we furtherly followed-up the enrolled participants to assess how long persisted the improvement of glycated haemoglobin (HbA1c%) and of RA disease activity.

RESULTS

After a mean follow-up of 18 months (15 participants in anakinra-group and 14 in TNFi-group), RA clinical response was retained in both groups (DAS28: 2.59±1.01 vs. 2.88±0.91; p=0.109). Concomitant glucocorticoids were reduced in both groups (2.01±0.71 vs. 3.01±0.87 mg/die; p=0.124), but a larger percentage of anakinra-treated participants discontinued such drugs (53.3% vs. 28.6%; p=0.004). There was no difference between anakinra and TNFi for HbA1c% (6.60±0.52 vs. 6.79±0.43; p=0.291), but a reduction of anti-diabetic drugs was observed in anakinra-treated participants (53.3% vs. 7.1%; p=0.008) whereas an increase of anti-diabetic therapies was needed in TNFi-treated ones. Significant correlations were also observed among HbA1c% with DAS28 and with C-reactive protein. Analysing the safety profile, only minor side effects were recorded.

CONCLUSIONS

Data deriving from the long-term extension of participants with RA and T2D, enrolled in the TRACK study, could suggest that the benefits of IL-1 inhibition on metabolic and inflammatory parameters could last longer than first 6 months of follow-up, but further studies are needed to confirm these findings.

摘要

目的

白细胞介素(IL)-1β被认为是类风湿关节炎(RA)和 2 型糖尿病(T2D)之间共同的致病介质。在 TRACK 研究中,患有这两种疾病的参与者被随机分配到白细胞介素-1 抑制剂(阿那白滞素)或肿瘤坏死因子抑制剂(TNFi)组。6 个月后,阿那白滞素诱导代谢和炎症参数的改善,导致研究提前停止。因此,我们旨在评估 IL-1 抑制作用持续的时间。

方法

由于 TRACK 因“早期获益”而提前停止,我们进一步随访入组患者,以评估糖化血红蛋白(HbA1c%)和 RA 疾病活动度改善持续的时间。

结果

在平均 18 个月的随访后(阿那白滞素组 15 例,TNFi 组 14 例),两组的 RA 临床缓解均得以维持(DAS28:2.59±1.01 vs. 2.88±0.91;p=0.109)。两组患者同时接受的糖皮质激素治疗均减少(2.01±0.71 vs. 3.01±0.87 mg/d;p=0.124),但阿那白滞素治疗组停药比例更高(53.3% vs. 28.6%;p=0.004)。阿那白滞素和 TNFi 对 HbA1c%的影响无差异(6.60±0.52 vs. 6.79±0.43;p=0.291),但阿那白滞素治疗组的降糖药物减少(53.3% vs. 7.1%;p=0.008),而 TNFi 治疗组需要增加降糖治疗。HbA1c%与 DAS28 和 C 反应蛋白之间也存在显著相关性。分析安全性概况,仅记录到轻微的副作用。

结论

从 TRACK 研究中入组的 RA 和 T2D 患者的长期随访中获得的数据提示,IL-1 抑制对代谢和炎症参数的获益可能持续时间长于 6 个月的随访期,但需要进一步研究来证实这些发现。

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