Home Philip, Lauand Felipe, Djaballah Khier, Li Xuan-Tony, Hafidh Khadija, Mehta Roopa, Faraoun Khadra, Anaforoğlu İnan, Serafini Paul, Pourrahmat Mir-Masoud
Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.
Sanofi, Paris, France.
Diabetes Obes Metab. 2025 Jun;27(6):3410-3418. doi: 10.1111/dom.16360. Epub 2025 Apr 2.
To estimate the relative treatment effect of iGlarLixi (a fixed-ratio combination of insulin glargine 100 U/mL plus lixisenatide) versus premixed insulin IDegAsp (insulin degludec plus insulin aspart) in people with type 2 diabetes (T2D) who advanced from basal insulin to iGlarLixi or IDegAsp in non-Asian studies.
Randomized controlled trials (RCTs) were identified in a systematic review by searching Embase (including congress abstracts from 2021 to 2023), MEDLINE® and CENTRAL on 10 October 2023. Treatment outcomes from non-Asian RCTs for people with T2D previously treated with basal insulin, who switched to iGlarLixi or IDegAsp, were compared using a network meta-analysis (NMA). Data analysis was performed using R, version 4.0.2.
The NMA included four RCTs (N = 2535). The results of the NMA showed that iGlarLixi (n = 810) was associated with a significantly greater reduction in HbA1c versus IDegAsp (n = 454) (mean difference [MD]: -0.39 [95% credible interval, CrI: -0.58, -0.21] %-units). iGlarLixi was also associated with a significantly greater likelihood of achieving an HbA1c of <7.0% (risk ratio: 1.42, 95% CrI: 1.18, 1.71). A greater reduction in postprandial glucose was observed with iGlarLixi versus IDegAsp (MD: -1.38 [95% CrI: -2.15, -0.63] mmol/L). A body weight benefit that favoured iGlarLixi versus IDegAsp was documented (MD: -1.54 [95% CrI: -2.26, -0.84] kg). Hypoglycaemia evaluation was inconclusive due to definitional differences between trials.
Once-daily iGlarLixi was associated with superior blood glucose control and body weight benefit compared with IDegAsp in insulin-experienced populations with T2D in non-Asian RCTs.
在非亚洲研究中,评估甘精胰岛素利司那肽固定比例复方制剂(甘精胰岛素100U/mL加利司那肽)与预混胰岛素德谷门冬胰岛素(德谷胰岛素加门冬胰岛素)相比,对从基础胰岛素转换为甘精胰岛素利司那肽或德谷门冬胰岛素的2型糖尿病(T2D)患者的相对治疗效果。
于2023年10月10日通过检索Embase(包括2021年至2023年的会议摘要)、MEDLINE®和CENTRAL进行系统评价,以识别随机对照试验(RCT)。使用网状Meta分析(NMA)比较非亚洲RCT中既往接受基础胰岛素治疗、转而使用甘精胰岛素利司那肽或德谷门冬胰岛素的T2D患者的治疗结局。使用R 4.0.2版本进行数据分析。
NMA纳入了4项RCT(N = 2535)。NMA结果显示,与德谷门冬胰岛素(n = 454)相比,甘精胰岛素利司那肽(n = 810)与糖化血红蛋白(HbA1c)的显著更大降幅相关(平均差值[MD]:-0.39[95%可信区间,CrI:-0.58,-0.21]%-单位)。甘精胰岛素利司那肽还与HbA1c<7.0%的显著更高可能性相关(风险比:1.42,95%CrI:1.18,1.71)。与德谷门冬胰岛素相比,甘精胰岛素利司那肽使餐后血糖有更大降幅(MD:-1.38[95%CrI:-2.15,-0.63]mmol/L)。记录到与德谷门冬胰岛素相比,甘精胰岛素利司那肽有体重获益(MD:-1.54[95%CrI:-2.26,-0.84]kg)。由于各试验之间的定义差异,低血糖评估尚无定论。
在非亚洲RCT中,对于有胰岛素治疗经验的T2D人群,每日一次的甘精胰岛素利司那肽与德谷门冬胰岛素相比,血糖控制更佳且有体重获益。