A Lower Baseline Urinary Glucose Excretion Predicts a Better Response to the Sodium Glucose Cotransporter 2 Inhibitor

被引:9
作者
Hwang, You-Cheol [1 ]
Kim, Jae Hyeon [2 ]
Lee, Byung-Wan [3 ]
Lee, Woo Je [4 ]
机构
[1] Kyung Hee Univ, Kyung Hee Univ Hosp Gangdong, Dept Med, Sch Med, Seoul, South Korea
[2] Sungkyunkwan Univ, Samsung Med Ctr, Dept Med, Sch Med, Seoul, South Korea
[3] Yonsei Univ, Severance Hosp, Dept Internal Med, Coll Med, 50 1 Yonsei Ro, Seoul 03722, South Korea
[4] Univ Ulsan, Asan Med Ctr, Dept Internal Med, Coll Med, 88 Olymp Ro 43 Gil, Seoul 05505, South Korea
关键词
Diabetes mellitus; type; 2; Glycosuria; Ipragliflozin; Sodium-glucose transporter 2; EFFICACY; SAFETY;
D O I
10.4093/dmj.2018.0257
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We aimed to identify the clinical variables associated with a better glucose-lowering response to the sodium glucose cotransporter 2 inhibitor ipragliflozin in people with type 2 diabetes mellitus (T2DM). We especially focused on urinary glucose excretion (UGE). This was a single-arm multicenter prospective study. A total of 92 people with T2DM aged 20 to 70 years with glycosylated hemoglobin (HbA1c) levels >= 7.0% and <= 9.5% were enrolled. Ipragliflozin (50 mg) was added to the background therapy for these people for 12 weeks. After 3 months treatment with ipragliflozin, the mean HbA1c levels were decreased from 7.6% to 6.9% and 62.0% of the people reached the HbA1c target of less than 7.0% (P< 0.001). In addition, body weight, blood pressure, and lipid parameters were improved after ipragliflozin treatment (all P<0.001). The baseline HbA1c (r=0.66, P<0.001) and morning spot urine glucose to creatinine ratio (r= -0.30, P=0.001) were independently associated with the HbA1c reduction. Ipragliflozin treatment for 12 weeks improves glycemic control and other metabolic parameters. A higher HbA1c and lower UGE at baseline predicts a better glucose-lowering efficacy of ipragliflozin.
引用
收藏
页码:898 / 905
页数:8
相关论文
共 10 条
[1]   Predictors of the response of HbAlc and body weight after SGLT2 inhibition [J].
Abe, T. ;
Matsubayashi, Y. ;
Yoshida, A. ;
Suganami, H. ;
Nojima, T. ;
Osawa, T. ;
Ishizawa, M. ;
Yamamoto, M. ;
Fujihara, K. ;
Tanaka, S. ;
Kaku, K. ;
Sone, H. .
DIABETES & METABOLISM, 2018, 44 (02) :172-174
[2]   Influence of Renal Function on the 52-Week Efficacy and Safety of the Sodium Glucose Cotransporter 2 Inhibitor Luseogliflozin in Japanese Patients with Type 2 Diabetes Mellitus [J].
Haneda, Masakazu ;
Seino, Yutaka ;
Inagaki, Nobuya ;
Kaku, Kohei ;
Sasaki, Takashi ;
Fukatsu, Atsushi ;
Kakiuchi, Haruka ;
Sato, Yuri ;
Sakai, Soichi ;
Samukawa, Yoshishige .
CLINICAL THERAPEUTICS, 2016, 38 (01) :66-88
[3]   A Novel Therapeutic Agent for Type 2 Diabetes Mellitus: SGLT2 Inhibitor [J].
Jung, Chang Hee ;
Jang, Jung Eun ;
Park, Joong-Yeol .
DIABETES & METABOLISM JOURNAL, 2014, 38 (04) :261-273
[4]   Factors predicting therapeutic efficacy of combination treatment with sitagliptin and metformin in type 2 diabetic patients: the COSMETIC study [J].
Lim, Soo ;
An, Jee Hyun ;
Shin, Hayley ;
Khang, Ah Reum ;
Lee, Yenna ;
Ahn, Hwa Young ;
Yoon, Ji Won ;
Kang, Seon Mee ;
Choi, Sung Hee ;
Cho, Young Min ;
Park, Kyong Soo ;
Jang, Hak Chul .
CLINICAL ENDOCRINOLOGY, 2012, 77 (02) :215-223
[5]   Glucose handling by the kidney [J].
Mather, Amanda ;
Pollock, Carol .
KIDNEY INTERNATIONAL, 2011, 79 :S1-S6
[6]   Better response to the SGLT2 inhibitor dapagliflozin in young adults with type 2 diabetes [J].
Nakamura, Yuta ;
Nagai, Yoshio ;
Terashima, Yuko ;
Nishine, Ami ;
Ishii, Satoshi ;
Kato, Hiroyuki ;
Ohta, Akio ;
Tanaka, Yasushi .
EXPERT OPINION ON PHARMACOTHERAPY, 2015, 16 (17) :2553-2559
[7]   Renal threshold for glucose reabsorption predicts diabetes improvement by sodium-glucose cotransporter 2 inhibitor therapy [J].
Osaki, Aya ;
Okada, Shuichi ;
Saito, Tsugumichi ;
Yamada, Eijiro ;
Ono, Kumeo ;
Niijima, Yawara ;
Hoshi, Hiroto ;
Yamada, Masanobu .
JOURNAL OF DIABETES INVESTIGATION, 2016, 7 (05) :751-754
[8]   Glucose transporters in human renal proximal tubular cells isolated from the urine of patients with non-insulin-dependent diabetes [J].
Rahmoune, H ;
Thompson, PW ;
Ward, JM ;
Smith, CD ;
Hong, GZ ;
Brown, J .
DIABETES, 2005, 54 (12) :3427-3434
[9]   SGLT2 inhibitors in the management of type 2 diabetes [J].
Reddy, R. P. Monica ;
Inzucchi, Silvio E. .
ENDOCRINE, 2016, 53 (02) :364-372
[10]   Safety, Pharmacokinetic, and Pharmacodynamic Profiles of Ipragliflozin (ASP1941), a Novel and Selective Inhibitor of Sodium-Dependent Glucose Co-Transporter 2, in Patients with Type 2 Diabetes Mellitus [J].
Schwartz, Sherwyn L. ;
Akinlade, Bola ;
Klasen, Sally ;
Kowalski, Donna ;
Zhang, Wenhui ;
Wilpshaar, Wim .
DIABETES TECHNOLOGY & THERAPEUTICS, 2011, 13 (12) :1219-1227