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