Use of SGLT2 inhibitors in type 2 diabetes: weighing the risks and benefits

被引:141
作者
Lupsa, Beatrice C. [1 ]
Inzucchi, Silvio E. [1 ]
机构
[1] Yale Univ, Sch Med, Sect Endocrinol, Yale New Haven Hosp, 333 Cedar St,FMP 106,POB 208020, New Haven, CT 06520 USA
关键词
Benefits; Cardiovascular; Fractures; Ketoacidosis; Renal; Review; Risks; SGLT2; inhibitors; Type; 2; diabetes; GLUCOSE COTRANSPORTER-2 INHIBITORS; DOUBLE-BLIND; ADD-ON; CARDIOVASCULAR MORTALITY; LOWERING DRUGS; CVD-REAL; EMPAGLIFLOZIN; MONOTHERAPY; MELLITUS; SAFETY;
D O I
10.1007/s00125-018-4663-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Sodium-glucose cotransporter 2 (SGLT2) inhibitors belong to a novel class of glucose-lowering medications that reduce plasma glucose concentrations by inhibiting glucose reabsorption by the kidney, inducing glucosuria. Their actions encompass reductions in HbA(1c), fasting and postprandial blood glucose levels, body weight and BP. To date, empagliflozin and canagliflozin have additionally been shown to improve cardiovascular outcomes in high-risk individuals and to slow the progression of diabetic kidney disease. Adverse effects associated with this class include urinary frequency, dehydration, genitourinary tract infections and, rarely, euglycaemic diabetic ketoacidosis. Of the SGLT2 inhibitors, only canagliflozin has been linked to a higher risk of lower-extremity amputations and bone fractures compared with placebo. Optimal prescribing of agents within this relatively new drug category requires a full understanding of their risks in addition to their benefits.
引用
收藏
页码:2118 / 2125
页数:8
相关论文
共 39 条
[2]   Empagliflozin decreases myocardial cytoplasmic Na+ through inhibition of the cardiac Na+/H+ exchanger in rats and rabbits [J].
Baartscheer, Antonius ;
Schumacher, Cees A. ;
Wust, Rob C. I. ;
Fiolet, Jan W. T. ;
Stienen, Ger J. M. ;
Coronel, Ruben ;
Zuurbier, Coert J. .
DIABETOLOGIA, 2017, 60 (03) :568-573
[3]   Canagliflozin: Effects in Overweight and Obese Subjects Without Diabetes Mellitus [J].
Bays, Harold E. ;
Weinstein, Richard ;
Law, Gordon ;
Canovatchel, William .
OBESITY, 2014, 22 (04) :1042-1049
[4]   Evaluation of Bone Mineral Density and Bone Biomarkers in Patients With Type 2 Diabetes Treated With Canagliflozin [J].
Bilezikian, John P. ;
Watts, Nelson B. ;
Usiskin, Keith ;
Polidori, David ;
Fung, Albert ;
Sullivan, Daniel ;
Rosenthal, Norm .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2016, 101 (01) :43-50
[5]   Cardiovascular mortality and morbidity in patients with type 2 diabetes following initiation of sodium-glucose co-transporter-2 inhibitors versus other glucose-lowering drugs (CVD-REAL Nordic): a multinational observational analysis [J].
Birkeland, Kare I. ;
Jorgensen, Marit E. ;
Carstensen, Bendix ;
Persson, Frederik ;
Gulseth, Hanne L. ;
Thuresson, Marcus ;
Fenici, Peter ;
Nathanson, David ;
Nystrom, Thomas ;
Eriksson, Jan W. ;
Bodegard, Johan ;
Norhammar, Anna .
LANCET DIABETES & ENDOCRINOLOGY, 2017, 5 (09) :709-717
[6]  
Center for Drug Evaluation and Research, 2013, APPL NUMB 2022930ORG
[7]   Use of Sodium Glucose Cotransporter 2 Inhibitors in the Hands of Cardiologists With Great Power Comes Great Responsibility [J].
Cherney, David Z. I. ;
Udell, Jacob A. .
CIRCULATION, 2016, 134 (24) :1915-1917
[8]   CV Protection in the EMPA-REG OUTCOME Trial: A "Thrifty Substrate" Hypothesis [J].
Ferrannini, Ele ;
Mark, Michael ;
Mayoux, Eric .
DIABETES CARE, 2016, 39 (07) :1108-1114
[9]   Metabolic response to sodium-glucose cotransporter 2 inhibition in type 2 diabetic patients [J].
Ferrannini, Ele ;
Muscelli, Elza ;
Frascerra, Silvia ;
Baldi, Simona ;
Mari, Andrea ;
Heise, Tim ;
Broedl, Uli C. ;
Woerle, Hans-Juergen .
JOURNAL OF CLINICAL INVESTIGATION, 2014, 124 (02) :499-508
[10]   Dapagliflozin Monotherapy in Type 2 Diabetic Patients With Inadequate Glycemic Control by Diet and Exercise A randomized, double-blind, placebo-controlled, phase 3 trial [J].
Ferrannini, Ele ;
Jimenez Ramos, Silvia ;
Salsali, Afshin ;
Tang, Weihua ;
List, James F. .
DIABETES CARE, 2010, 33 (10) :2217-2224