Sodium- Glucose Cotransporter 2 Inhibition and Glycemic Control in Type 1 Diabetes: Results of an 8-Week Open- Label Proof- ofConcept Trial

被引:187
作者
Perkins, Bruce A. [1 ]
Cherney, David Z. I. [2 ]
Partridge, Helen [1 ]
Soleymanlou, Nima [3 ]
Tschirhart, Holly [1 ]
Zinman, Bernard [1 ,4 ]
Fagan, Nora M. [5 ]
Kaspers, Stefan [6 ]
Woerle, Hans-Juergen [6 ]
Broedl, Uli C. [6 ]
Johansen, Odd-Erik [6 ]
机构
[1] Univ Toronto, Dept Med, Div Endocrinol, Toronto, ON, Canada
[2] Univ Toronto, Toronto Gen Hosp, Dept Med, Div Nephrol, Toronto, ON M5G 1L7, Canada
[3] Boehringer Ingelheim Canada Ltd Ltee, Burlington, ON, Canada
[4] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, New York, NY 10029 USA
[5] Boehringer Ingelheim Pharmaceut Inc, Ridgefield, CT USA
[6] Boehringer Ingelheim Pharma GmbH & Co KG, Ingelheim, Germany
关键词
SGLT-2; INHIBITOR; INSULIN; EMPAGLIFLOZIN; KETOACIDOSIS;
D O I
10.2337/dc13-2338
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVEAdjunctive-to-insulin therapy with sodium-glucose cotransporter 2 (SGLT2) inhibition may improve glycemic control in type 1 diabetes (T1D).RESEARCH DESIGN AND METHODSWe evaluated the glycemic efficacy and safety of empagliflozin 25 mg daily in 40 patients treated for 8 weeks in a single-arm open-label proof-of-concept trial (NCT01392560).RESULTSMean A1C decreased from 8.0 0.9% (64 +/- 10 mmol/mol) to 7.6 +/- 0.9% (60 +/- 10 mmol/mol) (P < 0.0001), fasting glucose from 9.0 +/- 4.3 to 7.0 +/- 3.2 mmol/L (P = 0.008), symptomatic hypoglycemia (<3.0 mmol/L) from 0.12 to 0.04 events per patient per day (P = 0.0004), and daily insulin dose from 54.7 +/- 20.4 to 45.8 +/- 18.8 units/day (P < 0.0001). Mean urinary excretion of glucose increased from 19 +/- 19 to 134 +/- 61 g/day (P < 0.0001). Weight decreased from 72.6 +/- 12.7 to 70.0 +/- 12.3 kg (P < 0.0001), and waist circumference decreased from 82.9 +/- 8.7 to 79.1 +/- 8.0 cm (P < 0.0001).CONCLUSIONSThis proof-of-concept study strongly supports a randomized clinical trial of adjunctive-to-insulin empagliflozin in patients with T1D.
引用
收藏
页码:1480 / 1483
页数:4
相关论文
共 15 条
  • [1] SHORT-TERM FASTING IS A MECHANISM FOR THE DEVELOPMENT OF EUGLYCEMIC KETOACIDOSIS DURING PERIODS OF INSULIN DEFICIENCY
    BURGE, MR
    HARDY, KJ
    SCHADE, DS
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1993, 76 (05) : 1192 - 1198
  • [2] Cherney DZI, 2013, CIRCULATION
  • [3] Systematic review of SGLT2 receptor inhibitors in dual or triple therapy in type 2 diabetes
    Clar, Christine
    Gill, James Alexander
    Court, Rachel
    Waugh, Norman
    [J]. BMJ OPEN, 2012, 2 (05):
  • [4] SGLT2 inhibition in diabetes mellitus: rationale and clinical prospects
    Ferrannini, Ele
    Solini, Anna
    [J]. NATURE REVIEWS ENDOCRINOLOGY, 2012, 8 (08) : 495 - 502
  • [5] Ferrannini EME, 2013, DIABETES S1, V62, P71
  • [6] Empagliflozin, a novel selective sodium glucose cotransporter-2 (SGLT-2) inhibitor: characterisation and comparison with other SGLT-2 inhibitors
    Grempler, R.
    Thomas, L.
    Eckhardt, M.
    Himmelsbach, F.
    Sauer, A.
    Sharp, D. E.
    Bakker, R. A.
    Mark, M.
    Klein, T.
    Eickelmann, P.
    [J]. DIABETES OBESITY & METABOLISM, 2012, 14 (01) : 83 - 90
  • [7] Diabetic ketoacidosis in pregnancy tends to occur at lower blood glucose levels: Case-control study and a case report of euglycemic diabetic ketoacidosis in pregnancy
    Guo, Rui-Xia
    Yang, Ling-Zhu
    Li, Liu-Xia
    Zhao, Xue-Ping
    [J]. JOURNAL OF OBSTETRICS AND GYNAECOLOGY RESEARCH, 2008, 34 (03) : 324 - 330
  • [8] Safety, tolerability, pharmacokinetics and pharmacodynamics following 4 weeks' treatment with empagliflozin once daily in patients with type 2 diabetes
    Heise, T.
    Seewaldt-Becker, E.
    Macha, S.
    Hantel, S.
    Pinnetti, S.
    Seman, L.
    Woerle, H. J.
    [J]. DIABETES OBESITY & METABOLISM, 2013, 15 (07) : 613 - 621
  • [9] Why do SGLT2 inhibitors inhibit only 30-50% of renal glucose reabsorption in humans?
    Liu, Jiwen
    Lee, TaeWeon
    DeFronzo, Ralph A.
    [J]. DIABETES, 2012, 61 (09) : 2199 - 2204
  • [10] Empagliflozin, a novel potent and selective SGLT-2 inhibitor, improves glycaemic control alone and in combination with insulin in streptozotocin-induced diabetic rats, a model of type 1 diabetes mellitus
    Luippold, G.
    Klein, T.
    Mark, M.
    Grempler, R.
    [J]. DIABETES OBESITY & METABOLISM, 2012, 14 (07) : 601 - 607