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在巴西1型糖尿病患者中,从每日两次基础胰岛素转换为每日一次的甘精胰岛素300 U/mL(Gla-300)的效果。

Effect of switching from twice-daily basal insulin to once-daily insulin glargine 300 U/mL (Gla-300) in Brazilian people with type 1 diabetes.

作者信息

Dualib Patricia Medici, Dib Sergio Atala, Augusto Gustavo Akerman, Truzzi Ana Cristina, de Paula Mauricio Aguiar, Réa Rosângela Roginski

机构信息

Escola Paulista de Medicina da Universidade Federal de São Paulo (EPM-Unifesp), São Paulo, Brazil.

Diabetes Center of the Endocrinology Division, Paulista School of Medicine - Federal University of São Paulo, Rua Estado de Israel 639, São Paulo, 04022-001, SP, Brazil.

出版信息

Diabetol Metab Syndr. 2024 Jul 9;16(1):152. doi: 10.1186/s13098-024-01385-x.

Abstract

BACKGROUND

Low adherence to the number of insulin injections and glycemic variability are among the challenges of insulin therapy in type 1 diabetes (T1D). The TOP1 study investigated the effect of switching from twice-daily (BID) basal insulin to once daily (OD) insulin glargine 300 U/mL (Gla-300) on glycemic control and quality of life.

METHODS

In this 28-week, phase 4 trial, people with T1D aged ≥ 18 years, who were treated with BID basal insulin in combination with prandial rapid-acting insulin for at least 1 year, and had HbA1c between 7.5% and 10.0%, were switched to Gla-300 OD as basal insulin. The present study aimed to evaluate the impact of this change on HbA1c, glycemic profile, treatment satisfaction and safety. The change in HbA1c from baseline to Week 24 was the primary endpoint.

RESULTS

One hundred and twenty-three people with T1D (mean age 37 ± 11 years; 54.5% female) were studied. The disease duration was 20.0 ± 9.8 years, baseline HbA1c and fasting plasma glucose (FPG) were 8.6 ± 0.7% and 201 ± 80.3 mg/dL, respectively. After switching from BID to OD insulin regimen, no significant change in HbA1c was observed from baseline to Week 24 (p = 0.873). There were significant reductions in fasting self-monitoring blood glucose (SMBG) from baseline to Week 24 (175 ± 42 vs. 156 ± 38 mg/dL; p < 0.0001), and in glycemic profile (8-point SMBG) at several time points. There was a significant decrease in the proportion of patients with at least one hypoglycemic event (p = 0.025), in numbers of hypoglycemic events per patient-years of any type (p = 0.036), symptomatic (p = 0.007), and confirmed ≤ 70 mg/dL events (p = 0.049) from run-in to the last 4 weeks on treatment. There were significant improvements in treatment satisfaction (p < 0.0001), perceived hyperglycemia (p < 0.0001) scores and satisfaction with the number of injections between post-run-in and Week 24, and a significant decrease in fear of hypoglycemia.

CONCLUSIONS

Switch from BID basal insulin to OD Gla-300 as part of basal bolus therapy in T1D resulted in similar glycemic control as measured by HbA1c, but provided significant improvements in SMBG, daily glucose profile, a lower incidence of hypoglycemia and increased patient satisfaction.

TRIAL REGISTRATION

NCT03406000.

摘要

背景

1型糖尿病(T1D)胰岛素治疗面临的挑战之一是胰岛素注射次数依从性低和血糖变异性。TOP1研究调查了从每日两次(BID)基础胰岛素转换为每日一次(OD)300 U/mL甘精胰岛素(Gla-300)对血糖控制和生活质量的影响。

方法

在这项为期28周的4期试验中,年龄≥18岁、接受BID基础胰岛素联合餐时速效胰岛素治疗至少1年且糖化血红蛋白(HbA1c)在7.5%至10.0%之间的T1D患者被转换为Gla-300 OD作为基础胰岛素。本研究旨在评估这一变化对HbA1c、血糖谱、治疗满意度和安全性的影响。从基线到第24周HbA1c的变化是主要终点。

结果

对123例T1D患者(平均年龄37±11岁;54.5%为女性)进行了研究。病程为20.0±9.8年,基线HbA1c和空腹血糖(FPG)分别为8.6±0.7%和201±80.3mg/dL。从BID胰岛素方案转换为OD胰岛素方案后,从基线到第24周HbA1c未观察到显著变化(p = 0.873)。从基线到第24周,空腹自我监测血糖(SMBG)显著降低(175±42 vs. 156±38mg/dL;p < 0.0001),并且在几个时间点的血糖谱(8点SMBG)也显著降低。从导入期到治疗的最后4周,至少发生一次低血糖事件的患者比例显著降低(p = 0.025),任何类型的每位患者每年低血糖事件数量显著降低(p = 0.036),有症状的低血糖事件数量显著降低(p = 0.007),确诊的≤70mg/dL低血糖事件数量显著降低(p = 0.049)。从导入期后到第24周,治疗满意度(p < 0.0001)、感知高血糖(p < 0.0001)评分以及对注射次数的满意度显著改善,对低血糖的恐惧显著降低。

结论

在T1D的基础-餐时胰岛素治疗中,从BID基础胰岛素转换为OD Gla-300导致以HbA1c衡量的血糖控制相似,但在SMBG、每日血糖谱、低血糖发生率降低和患者满意度提高方面有显著改善。

试验注册号

NCT03406000。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b38/11232174/3181f4b71539/13098_2024_1385_Fig1_HTML.jpg

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