Preventive effect of ipragliflozin on nocturnal hypoglycemia in patients with type 2 diabetes treated with basal-bolus insulin therapy: An open-label, single-center, parallel, randomized control study

被引:8
作者
Okajima, Fumitaka [1 ,2 ]
Nagamine, Tomoko [1 ,2 ]
Nakamura, Yuko [1 ,2 ]
Hattori, Naomi [1 ,2 ]
Sugihara, Hitoshi [2 ]
Emoto, Naoya [1 ,2 ]
机构
[1] Nippon Med Sch, Div Endocrinol, Dept Med, Chiba Hokusoh Hosp, Chiba, Japan
[2] Nippon Med Sch, Dept Endocrinol Diabet & Metab, Grad Sch Med, Tokyo, Japan
关键词
Basal-bolus insulin therapy; Nocturnal hypoglycemia; Sodium-glucose co-transporter 2 inhibitor; GLYCEMIC CONTROL; GLUCAGON; DAPAGLIFLOZIN; VILDAGLIPTIN; MORTALITY;
D O I
10.1111/jdi.12588
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The efficacy of the administration of sodium-glucose co-transporter 2 inhibitor or the co-administration of sodium-glucose co-transporter 2 inhibitor and dipeptidyl peptidase-4 inhibitor to insulin therapy is not well known. A total of 58 patients with type 2 diabetes, admitted for glycemic control, were randomized to basal-bolus insulin therapy (BBT) alone or BBT plus 50 mg ipragliflozin and/or 20 mg teneligliptin. Insulin doses were adjusted to maintain normal blood glucose levels. Plasma glucose profiles were estimated by continuous glucose monitoring before discharge. Required insulin doses were not significantly different among the treatment groups. The frequency of nocturnal hypoglycemia was significantly lower in the groups treated with ipragliflozin (6.5 +/- 10.6%) and ipragliflozin plus teneligliptin (6.9 +/- 14.3%) than in the group treated with BBT alone (42 +/- 43.6%). The administration of sodium-glucose co-transporter 2 inhibitor with or without dipeptidyl peptidase-4 inhibitor prevented nocturnal hypoglycemia in type 2 diabetes patients with BBT.
引用
收藏
页码:341 / 345
页数:5
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