2型糖尿病鼻内胰岛素对全身胰岛素的安全性:Memaid试验的双盲安慰剂对照亚研究

Archives of diabetes & obesity Pub Date : 2022-01-01 Epub Date: 2022-06-29
L Aponte Becerra, B Galindo Mendez, F Khan, V Lioutas, P Novak, C S Mantzoros, L H Ngo, V Novak
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引用次数: 0

摘要

目的:确定鼻内胰岛素(INI)在接受全身胰岛素治疗的MemAID试验参与者中的安全性。材料和方法:这项随机、双盲试验包括24周的INI或安慰剂治疗,每天一次,24周随访。安全性结果包括:1)基线和治疗期间连续血糖监测(CGM)对血糖变异性、低血糖发作的短期影响。2) INI/安慰剂治疗和治疗后随访对糖代谢和体重的长期影响。在86名筛选的受试者中,14名被随机分配,9名(5名INI, 4名安慰剂)在基线和治疗期间完成了CGM, 5名(2名INI, 3名安慰剂)完成了治疗和随访。结果:INI是安全的,与严重不良事件、低血糖发作或体重增加无关。注射INI对毛细血管血糖无明显影响。与基线相比,INI降低了CGM的血糖变异性。在INI治疗中,有降低HbA1c、血糖和胰岛素的长期趋势。未观察到与皮下胰岛素的相互作用。结论:INI对于接受全身性胰岛素治疗的老年糖尿病患者是安全的,并且与不良事件、低血糖或体重增加无关。未来的研究需要确定INI是否可以降低血糖变异性,改善胰岛素敏感性,从而潜在地减轻该人群的糖尿病负担。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Safety of Intranasal Insulin in Type 2 Diabetes on Systemic Insulin: A Double-Blinded Placebo-Controlled Sub-Study of Memaid Trial.

Safety of Intranasal Insulin in Type 2 Diabetes on Systemic Insulin: A Double-Blinded Placebo-Controlled Sub-Study of Memaid Trial.

Safety of Intranasal Insulin in Type 2 Diabetes on Systemic Insulin: A Double-Blinded Placebo-Controlled Sub-Study of Memaid Trial.

Safety of Intranasal Insulin in Type 2 Diabetes on Systemic Insulin: A Double-Blinded Placebo-Controlled Sub-Study of Memaid Trial.

Aims: To determine safety of intranasal insulin (INI) in MemAID trial participants with diabetes treated with systemic insulins.

Materials and methods: This randomized, double-blinded trial consisted of 24-week INI or placebo treatment once daily and 24-week follow-up. Safety outcomes were: 1) Short-term effects on glycemic variability, hypoglycemic episodes on continuous glucose monitoring (CGM) at baseline and on-treatment. 2) Long-term effects on glucose metabolism and weight on INI/placebo treatment and post-treatment follow-up. Of 86 screened subjects, 14 were randomized, 9 (5 INI, 4 Placebo) completed CGM at baseline and on-treatment, and 5 (2 INI, 3 Placebo) completed treatment and follow-up.

Results: INI was safe and was not associated with serious adverse events, hypoglycemic episodes or weight gain. INI administration did not acutely affect capillary glucose. Glycemic variability on CGM decreased with INI, compared to baseline. On INI treatment, there was a long-term trend toward lower HbA1c, plasma glucose and insulin. No interactions with subcutaneous insulins were observed.

Conclusions: INI is safe in older people with diabetes treated with systemic insulins, and it is not associated with adverse events, hypoglycemia or weight gain. Future studies are needed to determine whether INI administration can reduce glycemic variability, improve insulin sensitivity and thus potentially lessen diabetes burden in this population.

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