Division of Immunology and Rheumatology, Stanford University Medical Center, 1000 Welch Road, Suite 203, Palo Alto, CA, 94304, USA.
Charité University Medicine, Free University and Humboldt University of Berlin, Berlin, Germany.
Arthritis Res Ther. 2020 Sep 9;22(1):206. doi: 10.1186/s13075-020-02229-5.
Diabetes is common in patients with rheumatoid arthritis (RA). Interleukin (IL)-6 is implicated in both the pathogenesis of RA and in glucose homeostasis; this post hoc analysis investigated the effects of IL-6 receptor vs. tumour necrosis factor inhibition on glycosylated haemoglobin (HbA1c) in patients with RA with or without diabetes.
Data were from two placebo-controlled phase III studies of subcutaneous sarilumab 150/200 mg q2w + methotrexate or conventional synthetic disease-modifying antirheumatic drugs (csDMARDs) and a phase III monotherapy study of sarilumab 200 mg q2w vs. adalimumab 40 mg q2w. Patients with diabetes were identified by medical history or use of antidiabetic medication (patients with HbA1c ≥ 9% were excluded from all three studies). HbA1c was measured at baseline and weeks 12/24. Safety and efficacy were assessed in RA patients with or without diabetes.
Patients with diabetes (n = 184) were older, weighed more and exhibited higher RA disease activity than patients without diabetes (n = 1928). Regardless of diabetes status, in patients on background csDMARDs, least squares (LS) mean difference (95% CI) in change from baseline in HbA1c for sarilumab 150 mg/200 mg vs. placebo at week 24 was - 0.28 (- 0.40, - 0.16; nominal p < 0.0001) and - 0.42 (- 0.54, - 0.31; nominal p < 0.0001), respectively. Without csDMARDs, LS mean difference for sarilumab 200 mg vs. adalimumab 40 mg at week 24 was - 0.13 (- 0.22, - 0.04; nominal p = 0.0043). Greater reduction in HbA1c than placebo or adalimumab was observed at week 24 with sarilumab in patients with diabetes and/or baseline HbA1c ≥ 7%. There was no correlation between baseline/change from baseline in HbA1c and baseline/change from baseline in C-reactive protein, 28-joint Disease Activity Score, or haemoglobin, nor between HbA1c change from baseline and baseline glucocorticoid use. Medical history of diabetes or use of diabetes treatments had limited impact on safety and efficacy of sarilumab and was consistent with overall phase III findings in patients with RA.
In post hoc analyses, sarilumab was associated with a greater reduction in HbA1c than csDMARDs or adalimumab, independent of sarilumab anti-inflammatory effects. Prospective studies are required to further assess these preliminary findings.
ClinTrials.gov NCT01061736: date of registration February 03, 2010; ClinTrials.gov NCT01709578: date of registration October 18, 2012; ClinTrials.gov NCT02332590: date of registration January 07, 2015.
糖尿病在类风湿关节炎(RA)患者中很常见。白细胞介素(IL)-6 既参与 RA 的发病机制,也参与葡萄糖稳态;本事后分析研究了 IL-6 受体与肿瘤坏死因子抑制对合并或不合并糖尿病的 RA 患者糖化血红蛋白(HbA1c)的影响。
数据来自皮下注射 sarilumab 150/200mg q2w+甲氨蝶呤或传统合成疾病修饰抗风湿药物(csDMARDs)的两项安慰剂对照 III 期研究,以及 sarilumab 200mg q2w 与阿达木单抗 40mg q2w 的 III 期单药研究。通过病史或使用抗糖尿病药物确定糖尿病患者(所有三项研究均排除 HbA1c≥9%的患者)。在合并或不合并糖尿病的 RA 患者中评估 HbA1c 的基线和第 12/24 周的变化。
合并糖尿病的患者(n=184)年龄较大,体重较重,且 RA 疾病活动度高于不合并糖尿病的患者(n=1928)。无论糖尿病状态如何,在接受背景 csDMARDs 的患者中,与安慰剂相比,sarilumab 150mg/200mg 在第 24 周时 HbA1c 的 LS 均值差值(95%CI)为-0.28(-0.40,-0.16;名义 p<0.0001)和-0.42(-0.54,-0.31;名义 p<0.0001)。无 csDMARDs 时,第 24 周时 sarilumab 与阿达木单抗的 LS 均值差值为-0.13(-0.22,-0.04;名义 p=0.0043)。与安慰剂或阿达木单抗相比,在合并或不合并糖尿病以及基线 HbA1c≥7%的患者中,在第 24 周时,sarilumab 可更显著地降低 HbA1c。在基线和从基线的变化中,HbA1c 与 C 反应蛋白、28 关节疾病活动度或血红蛋白无相关性,且 HbA1c 从基线的变化与基线糖皮质激素使用无相关性。糖尿病病史或糖尿病治疗对 sarilumab 的安全性和疗效的影响有限,与 RA 患者的整体 III 期研究结果一致。
事后分析显示,sarilumab 与 csDMARDs 或阿达木单抗相比,能更显著地降低 HbA1c,且独立于 sarilumab 的抗炎作用。需要前瞻性研究进一步评估这些初步发现。
ClinicalTrials.gov NCT01061736:注册日期 2010 年 2 月 3 日;ClinicalTrials.gov NCT01709578:注册日期 2012 年 10 月 18 日;ClinicalTrials.gov NCT02332590:注册日期 2015 年 1 月 7 日。