Better response to the SGLT2 inhibitor dapagliflozin in young adults with type 2 diabetes

被引:12
作者
Nakamura, Yuta [1 ]
Nagai, Yoshio [1 ]
Terashima, Yuko [1 ]
Nishine, Ami [1 ]
Ishii, Satoshi [1 ]
Kato, Hiroyuki [1 ]
Ohta, Akio [1 ]
Tanaka, Yasushi [1 ]
机构
[1] St Marianna Univ, Sch Med, Div Endocrinol & Metab, Dept Internal Med,Miyamae Ku, Kawasaki, Kanagawa 2168511, Japan
关键词
continuous glucose monitoring; dapagliflozin; renal threshold of glucose; SGLT2; inhibitor; type; 2; diabetes; COTRANSPORTER; 2; INHIBITORS; RENAL GLUCOSE EXCRETION; BLOOD-GLUCOSE; MELLITUS; THRESHOLD; CANAGLIFLOZIN; TRANSPORTERS; REABSORPTION; NEPHROPATHY; SERUM;
D O I
10.1517/14656566.2015.1101450
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Background and aim: A variation of the response to Sodium glucose co-transporter 2 (SGLT2) inhibitors with age has not been investigated in patients with diabetes. The aim of this study was to assess renal threshold of glucose (RTg) before and after administration of an SGLT2 inhibitor in young adult patients (40years) and older adult patients (>40years) with type 2 diabetes (T2DM). Subjects and methods: Twenty Japanese patients with T2DM were enrolled. Baseline data were obtained on the first day and dapagliflozin (5mg) was administered at 6:00 on the second day. Glucose excursions were assessed by continuous glucose monitoring and urine samples were collected every hour during the daytime (7:00 to 15:00) on both days. RTg was estimated from the regression line of the scatter plot of the hourly mean glucose concentrations. Results: After a single dose of dapagliflozin, RTg decreased from 121.5 to 6.1mg/dl in the young adult group and from 151.0mg/dl to -15.8mg/dl in the older group. After dapagliflozin, the slope of the regression line was significantly steeper in the young adult group. Conclusion: Dapagliflozin was more effective in young patients because they showed a larger response of urinary glucose excretion.
引用
收藏
页码:2553 / 2559
页数:7
相关论文
共 23 条
[1]
Novel Hypothesis to Explain Why SGLT2 Inhibitors Inhibit Only 30-50% of Filtered Glucose Load in Humans [J].
Abdul-Ghani, Muhammad A. ;
DeFronzo, Ralph A. ;
Norton, Luke .
DIABETES, 2013, 62 (10) :3324-3328
[2]
Role of Sodium-Glucose Cotransporter 2 (SGLT 2) Inhibitors in the Treatment of Type 2 Diabetes [J].
Abdul-Ghani, Muhammad A. ;
Norton, Luke ;
DeFronzo, Ralph A. .
ENDOCRINE REVIEWS, 2011, 32 (04) :515-531
[3]
No Ghrelin Response to Oral Glucose in Diabetes Mellitus with Gastroparesis [J].
Asai, Shiko ;
Katabami, Takuyuki ;
Obi, Naoko ;
Matsui, Tomoya ;
Kato, Hiroyuki ;
Obi, Ryusei ;
Ogawa, Yutaka ;
Kawata, Takehiro ;
Takama, Haruyuki ;
Ohta, Akio ;
Tanaka, Yasushi .
ENDOCRINE JOURNAL, 2009, 56 (01) :79-87
[4]
Renal glucose reabsorption inhibitors to treat diabetes [J].
Bailey, Clifford J. .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2011, 32 (02) :63-71
[5]
BONDAR RJL, 1974, CLIN CHEM, V20, P586
[6]
RENAL GLUCOSE THRESHOLD VARIATIONS WITH AGE [J].
BUTTERFIELD, WJ ;
KEEN, H ;
WHICHELOW, MJ .
BMJ-BRITISH MEDICAL JOURNAL, 1967, 4 (5578) :505-+
[7]
The role of the kidneys in glucose homeostasis: a new path towards normalizing glycaemia [J].
DeFronzo, R. A. ;
Davidson, J. A. ;
Del Prato, S. .
DIABETES OBESITY & METABOLISM, 2012, 14 (01) :5-14
[8]
Characterization of Renal Glucose Reabsorption in Response to Dapagliflozin in Healthy Subjects and Subjects With Type 2 Diabetes [J].
DeFronzo, Ralph A. ;
Hompesch, Marcus ;
Kasichayanula, Sreeneeranj ;
Liu, Xiaoni ;
Hong, Ying ;
Pfister, Marc ;
Morrow, Linda A. ;
Leslie, Bruce R. ;
Boulton, David W. ;
Ching, Agatha ;
LaCreta, Frank P. ;
Griffen, Steven C. .
DIABETES CARE, 2013, 36 (10) :3169-3176
[9]
EFFECT OF DIABETES AND INSULIN ON THE MAXIMUM CAPACITY OF THE RENAL TUBULES TO REABSORB GLUCOSE [J].
FARBER, SJ ;
BERGER, EY ;
EARLE, DP .
JOURNAL OF CLINICAL INVESTIGATION, 1951, 30 (02) :125-129
[10]
A new Classification of Diabetic Nephropathy 2014: a report from Joint Committee on Diabetic Nephropathy [J].
Haneda, Masakazu ;
Utsunomiya, Kazunori ;
Koya, Daisuke ;
Babazono, Tetsuya ;
Moriya, Tatsumi ;
Makino, Hirofumi ;
Kimura, Kenjiro ;
Suzuki, Yoshiki ;
Wada, Takashi ;
Ogawa, Susumu ;
Inaba, Masaaki ;
Kanno, Yoshihiko ;
Shigematsu, Takashi ;
Masakane, Ikuto ;
Tsuchiya, Ken ;
Honda, Keiko ;
Ichikawa, Kazuko ;
Shide, Kenichiro .
JOURNAL OF DIABETES INVESTIGATION, 2015, 6 (02) :242-246