Switching From Daily DPP-4 Inhibitor to Once-Weekly GLP-1 Receptor Activator Dulaglutide Significantly Ameliorates Glycemic Control in Subjects With Poorly Controlled Type 2 Diabetes Mellitus: A Retrospective Observational Study.
Switching From Daily DPP-4 Inhibitor to Once-Weekly GLP-1 Receptor Activator Dulaglutide Significantly Ameliorates Glycemic Control in Subjects With Poorly Controlled Type 2 Diabetes Mellitus: A Retrospective Observational Study.
复制标题
DOI:
10.3389/fendo.2021.714447
复制
发表时间:
2021
影响因子:
5.2
通讯作者:
Kaneto H
中科院分区:
文献类型:
--
作者:
Sanada J;Kimura T;Shimoda M;Tomita A;Fushimi Y;Kinoshita T;Obata A;Okauchi S;Hirukawa H;Kohara K;Tatsumi F;Nakanishi S;Mune T;Kaku K;Kaneto H
At present, daily DPP-4 inhibitors are quite frequently prescribed in subjects with type 2 diabetes mellitus (T2DM). Recently, it has been drawing much attention that once-weekly incretin-based injection dulaglutide was developed. In this study, we aimed to examine the possible effects of once-weekly GLP-1 receptor activator (GLP-1RA) dulaglutide on glycemic control as well as various metabolic parameters. We made a direct comparison between the effect of daily DPP-4 inhibitor and once-weekly dulaglutide on glycemic control in “study 1 (pre–post comparison)” and set the control group using the propensity score matching method in “study 2”. In study 1, switching from daily DPP-4 inhibitor to dulaglutide significantly ameliorated glycemic control in subjects with T2DM. Such effects were more obvious in poorly controlled subjects. After 1:1 propensity score matching, the switching group improved glycemic control compared with the non-switching group in study 2. We should bear in mind that switching from daily DPP-4 inhibitor to once-weekly GLP-1RA dulaglutide exerts more favorable effects on glycemic control regardless of age, body weight, and duration of diabetes in subjects with T2DM, especially when we fail to obtain good glycemic control with daily DPP-4 inhibitor.
登录
查看更多内容
DOI:
10.1056/nejmoa1603827
发表时间:
2016-07-28
期刊:
The New England journal of medicine
影响因子:
--
作者:
Marso SP;Daniels GH;Brown-Frandsen K;Kristensen P;Mann JF;Nauck MA;Nissen SE;Pocock S;Poulter NR;Ravn LS;Steinberg WM;Stockner M;Zinman B;Bergenstal RM;Buse JB;LEADER Steering Committee;LEADER Trial Investigators
通讯作者:
LEADER Trial Investigators
影响因子:
168.9
作者:
Turner, RC;Holman, RR;Ward, JD
通讯作者:
Ward, JD
影响因子:
158.5
作者:
Gaede, Peter;Lund-Andersen, Henrik;Pedersen, Oluf
通讯作者:
Pedersen, Oluf
影响因子:
8.2
作者:
Davies, Melanie J.;D'Alessio, David A.;Buse, John B.
通讯作者:
Buse, John B.
DOI:
10.1111/dom.12005
发表时间:
2013-02
期刊:
Diabetes, obesity & metabolism
影响因子:
--
作者:
Hamamoto S;Kanda Y;Shimoda M;Tatsumi F;Kohara K;Tawaramoto K;Hashiramoto M;Kaku K
通讯作者:
Kaku K