Bostandzic Amela Dizdarevic, Beslic Vanja Karlovic, Surkovic Ismana, Balic Sefkija, Dujic Tanja, Asimi Zelija Velija, Burekovic Azra
Clinic for Nuclear Medicine and Endocrinology, Clinical Center University of Sarajevo, Sarajevo, Bosnia and Herzegovina.
Faculty of Pharmacy, University of Sarajevo, Sarajevo, Bosnia and Herzegovina.
Med Arch. 2022 Apr;76(2):96-100. doi: 10.5455/medarh.2022.76.96-100.
IDegLira( fixed combination of GLP 1 receptor agonist and insulin) has been shown to be effective in improving the glucoregulation in patients previously treated with oral therapy as well as individual components, GLP-1 receptor agonist or basal insulin.
The aim of this study is to examine the parameters of metabolic control in patients treated with IDegLira who were previously treated with premix insulin in several daily doses and to compare them with patients whose premix insulin dose was increased.
The study included 100 patients who had been previously treated with two or three daily doses of premix insulin. Half of the patients were switched to IdegLira( group I), and half (group II) had their insulin dose increased according to the clinical assessment of the physician. Fasting glucose, 2h postprandial glucose, HbA1c, BMI and insulin dose were determined at baseline and at follow-up after 6 months.
Patients treated with IDegLira compared to patients whose insulin dose was increased achieved significantly lower fasting glucose (p <0.001), postprandial glucose (p <0.001), HbA1c (p <0.001), BMI (p <0.001) with a significantly lower insulin dose (p <0.001). Comparison of the same parameters within the groups of patients at the beginning and after 6 months showed that patients who were switched from insulin premix to IDegLira achieved significantly lower fasting blood glucose (p <0.001), postprandial glucose (p <0.001), HbA1c (p < 0.001), BMI (p <0.001) with significantly lower insulin dose within the fixed combination (p <0.001). Patients with gradually increased insulin dose achieved significant reduction in fasting glucose (p = 0.021) and postprandial glucose (p = 0.036),but with a significantly higher insulin dose (p = 0.005). There was also a slight increase in BMI that was not statistically significant (p = 0.267).
The obtained data suggest that switching patients from a complex insulin regimen to a fixed combination of basal insulin and GLP 1 receptor agonist in comparison to increases in insulin dose results in a significant improvement in fasting glucose, postprandial glucose, HbA1c, and BMI. The results were achieved with a significantly lower daily insulin dose.
德谷胰岛素利拉鲁肽(胰高血糖素样肽-1受体激动剂与胰岛素的固定复方制剂)已被证明可有效改善先前接受口服治疗以及使用单一成分(胰高血糖素样肽-1受体激动剂或基础胰岛素)治疗的患者的血糖调节。
本研究旨在检查曾每日多次注射预混胰岛素治疗的患者接受德谷胰岛素利拉鲁肽治疗后的代谢控制参数,并将其与预混胰岛素剂量增加的患者进行比较。
本研究纳入100例曾每日注射两次或三次预混胰岛素的患者。其中一半患者换用德谷胰岛素利拉鲁肽(I组),另一半(II组)根据医生的临床评估增加胰岛素剂量。在基线和6个月随访时测定空腹血糖、餐后2小时血糖、糖化血红蛋白、体重指数和胰岛素剂量。
与胰岛素剂量增加的患者相比,接受德谷胰岛素利拉鲁肽治疗的患者空腹血糖(p<0.001)、餐后血糖(p<0.001)、糖化血红蛋白(p<0.001)、体重指数(p<0.001)显著降低,胰岛素剂量也显著降低(p<0.001)。对两组患者治疗开始时和6个月后的相同参数进行比较,结果显示,从预混胰岛素转换为德谷胰岛素利拉鲁肽治疗的患者空腹血糖(p<0.001)、餐后血糖(p<0.001)、糖化血红蛋白(p<0.001)、体重指数(p<0.001)显著降低;在固定复方制剂中,胰岛素剂量也显著降低(p<0.001)。胰岛素剂量逐渐增加的患者空腹血糖(p=0.021)和餐后血糖(p=0.036)显著降低,但胰岛素剂量显著更高(p=0.005)。体重指数也有轻微增加,但无统计学意义(p=0.267)。
所得数据表明,与增加胰岛素剂量相比,将患者从复杂胰岛素治疗方案转换为基础胰岛素与胰高血糖素样肽-1受体激动剂的固定复方制剂可显著改善空腹血糖、餐后血糖、糖化血红蛋白和体重指数。且达到这些结果所需的每日胰岛素剂量显著更低。