Luseogliflozin for the treatment of type 2 diabetes

被引:27
作者
Seino, Yutaka [1 ]
机构
[1] Kansai Elect Power Hosp, Fukushima Ku, Osaka, JP 5530003, Japan
关键词
luseogliflozin; sodium glucose cotransporter 2 inhibitor; sodium glucose cotransport; type 2 diabetes mellitus; 2; SGLT2; INHIBITOR; JAPANESE PATIENTS; DOUBLE-BLIND; MELLITUS; DAPAGLIFLOZIN; ASSOCIATION; MANAGEMENT; SAFETY; POTENT; TS-071;
D O I
10.1517/14656566.2014.978290
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Sodium glucose cotransporter 2 (SGLT2) inhibitors are expected to provide adequate glycemic control, and be safe and well tolerated, for treating type 2 diabetes mellitus (T2DM). Luseogliflozin is a highly selective SGLT2 inhibitor that was recently approved for marketing and launched in Japan to treat T2DM. Areas covered: This review summarizes the published data regarding the mechanism of action, clinical efficacy, and safety of luseogliflozin for treating T2DM. Other potential benefits of luseogliflozin, including lowering body weight and blood pressure, beyond its glucose-lowering effects are also discussed. Expert opinion: Luseogliflozin lowers plasma glucose concentration and body weight, and has beneficial effects on other clinically relevant parameters, including blood pressure and uric acid, in patients with T2DM. Although it had a good safety profile in clinical trials, there may be some safety concerns, including a possible decrease in muscle mass and an increase in ketone bodies. Therefore, careful administration and consideration of its benefit-risk balance are necessary. When using luseogliflozin, it is important to select appropriate patients and to adhere to its guidelines for use. If used correctly, luseogliflozin is expected to be positioned as a new type of oral hypoglycemic drug for treating T2DM.
引用
收藏
页码:2741 / 2749
页数:9
相关论文
共 27 条
  • [1] DPP-4 inhibition and islet function
    Ahren, Bo
    [J]. JOURNAL OF DIABETES INVESTIGATION, 2012, 3 (01): : 3 - 10
  • [2] [Anonymous], 2014, PHARM INT SUPPL PACK
  • [3] [Anonymous], 2014, LUS TABL 2 5 5 MG PA
  • [4] Chino Y, 2011, 26 JSSX ANN M 16 18
  • [5] 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):
  • [6] AMERICAN ASSOCIATION OF CLINICAL ENDOCRINOLOGISTS' COMPREHENSIVE DIABETES MANAGEMENT ALGORITHM 2013 CONSENSUS STATEMENT - EXECUTIVE SUMMARY
    Garber, Alan J.
    Abrahamson, Martin J.
    Barzilay, Joshua I.
    Blonde, Lawrence
    Bloomgarden, Zachary T.
    Bush, Michael A.
    Dagogo-Jack, Samuel
    Davidson, Michael B.
    Einhorn, Daniel
    Garvey, W. Timothy
    Grunberger, George
    Handelsman, Yehuda
    Hirsch, Irl B.
    Jellinger, Paul S.
    McGill, Janet B.
    Mechanick, Jeffrey I.
    Rosenblit, Paul D.
    Umpierrez, Guillermo E.
    Davidson, Michael H.
    [J]. ENDOCRINE PRACTICE, 2013, 19 (03) : 536 - 547
  • [7] Haneda M, 2012, 48 EUR ASS STUD DIAB
  • [8] International Diabetes Federation, IDF DIABETES ATLAS
  • [9] Management of Hyperglycemia in Type 2 Diabetes: A Patient-Centered Approach
    Inzucchi, Silvio E.
    Bergenstal, Richard M.
    Buse, John B.
    Diamant, Michaela
    Ferrannini, Ele
    Nauck, Michael
    Peters, Anne L.
    Tsapas, Apostolos
    Wender, Richard
    Matthews, David R.
    [J]. DIABETES CARE, 2012, 35 (06) : 1364 - 1379
  • [10] Urinary tract infections in patients with diabetes treated with dapagliflozin
    Johnsson, Kristina M.
    Ptaszynska, Agata
    Schmitz, Bridget
    Sugg, Jennifer
    Parikh, Shamik J.
    List, James F.
    [J]. JOURNAL OF DIABETES AND ITS COMPLICATIONS, 2013, 27 (05) : 473 - 478