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甘精胰岛素Gla-300在初治2型糖尿病患者真实临床环境中的有效性和安全性——GOAL_RO试验

Effectiveness and safety of insulin glargine Gla-300 in insulin-naïve type 2 diabetes subjects in a real-life setting-the GOAL_RO trial.

作者信息

Stegaru Daniela, Nicodim Simona, Vladu Delia, Guțu Olimpia, Onaca Adriana, Pîrvu Florina, Moise Mihaela, Guja Cristian

机构信息

Department of Diabetes, Nutrition and Metabolic Diseases, "Carol Davila" University of Medicine and Pharmacy, Bucharest, Romania.

Emergency Clinical County Hospital Constanța, Constanța, Romania.

出版信息

Ann Transl Med. 2021 Jan;9(2):105. doi: 10.21037/atm-20-4533.

Abstract

BACKGROUND

Basal insulin is the first choice for insulin initiation in type 2 diabetes (T2DM), with the second generation of basal insulin analogues having a lower risk of hypoglycemia compared to the first generation of basal insulins. The aim of our study was to assess on a large cohort of insulin-naïve T2DM subjects the effectiveness and safety of insulin glargine 300 U/mL (Gla-300) in a real-life setting.

METHODS

This was a multicenter, prospective, non-interventional, 24 weeks, 3 visits (baseline, 3 and 6 months) trial performed in adult T2DM subjects not achieving glycemic target (HbA1c >7%) with prior oral or GLP-1 RA therapy. The study included 1,095 subjects (55.2% M/44.8% F) in 124 study sites. Mean (±SD) age was 61.1±8.5 years while mean duration of diabetes was 8.8±5.2 years. Mean BMI was 31.7±5.4 kg/m with 91.2% being overweight or obese. Baseline diabetes treatment included metformin (88.4% of subjects), sulphonylureas (75.4%), DPP-4i (16.7%) and GLP-1 RAs (8%). Comparison between quantitative variables was made with the paired sample test.

RESULTS

Mean HbA1c at baseline was 9.8%±1.7% with a mean fasting plasma glucose (FBG) of 231.5±67.4 mg/dL. Mean HbA1c decreased to 7.7%±1.2% at 6 months with a mean change from baseline of -2.1% (P<0.001). Overall, 30.7% of subjects reached the HbA1c target of 7%. Final mean dose of Gla-300 was 0.4 IU/kg/day. Mean weight gain was 0.4 kg over 6 months. Adverse events (AEs) were reported by 11.1% of subjects with 2.3% reporting serious adverse events (SAEs). Overall, 4.4% of subjects reporting at least one event of symptomatic or confirmed hypoglycemia. Only 7 episodes of nocturnal and one of severe hypoglycemia were reported.

CONCLUSIONS

In conclusion, a significant 2.1% decrease of HbA1c was recorded after 6 months of treatment with Gla-300 with no unexpected safety signals, low risk of hypoglycemia and modest weight gain.

摘要

背景

基础胰岛素是2型糖尿病(T2DM)起始胰岛素治疗的首选,与第一代基础胰岛素相比,第二代基础胰岛素类似物低血糖风险更低。我们研究的目的是在一大群初治T2DM受试者中评估300 U/mL甘精胰岛素(Gla-300)在现实生活中的有效性和安全性。

方法

这是一项多中心、前瞻性、非干预性、为期24周、分3次访视(基线、3个月和6个月)的试验,在接受过口服或GLP-1受体激动剂(RA)治疗但未达到血糖目标(糖化血红蛋白[HbA1c]>7%)的成年T2DM受试者中进行。该研究在124个研究地点纳入了1095名受试者(男性占55.2%/女性占44.8%)。平均(±标准差)年龄为61.1±8.5岁,糖尿病平均病程为8.8±5.2年。平均体重指数(BMI)为31.7±5.4 kg/m²,91.2%为超重或肥胖。基线糖尿病治疗包括二甲双胍(88.4%的受试者)、磺脲类药物(75.4%)、二肽基肽酶-4抑制剂(DPP-4i,16.7%)和GLP-1 RAs(8%)。定量变量之间采用配对样本t检验进行比较。

结果

基线时平均HbA1c为9.8%±1.7% 平均空腹血糖(FBG)为231.5±67.4 mg/dL。6个月时平均HbA1c降至7.7%±1.2%,与基线相比平均变化为-2.1%(P<0.001)。总体而言,30.7%的受试者达到了HbA1c目标值7%。Gla-300的最终平均剂量为0.4 IU/kg/天。6个月内平均体重增加0.4 kg。11.1%的受试者报告了不良事件(AE),2.3%的受试者报告了严重不良事件(SAE)。总体而言,4.4%的受试者报告了至少一次有症状或确诊的低血糖事件。仅报告了夜间低血糖7次和严重低血糖1次。

结论

总之,用Gla-300治疗6个月后,HbA1c显著降低了2.1%,没有意外的安全信号,低血糖风险低,体重增加适度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c24/7867914/664771e3641f/atm-09-02-105-f1.jpg

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