Effects of SGLT2 inhibitors on weight loss in patients with type 2 diabetes mellitus

被引:2
作者
Ribola, F. A. [1 ]
Cancado, F. B. [1 ]
Schoueri, J. H. M. [1 ]
De Toni, V. F. [1 ]
Medeiros, V. H. R. [1 ]
Feder, D. [1 ]
机构
[1] ABC Med Sch, Dept Pharmacol, Sao Paulo, Brazil
关键词
Sodium-glucose transporter 2; Diabetes mellitus; T2DM; Weight loss; Hyperglycemia; GLUCOSE COTRANSPORTER 2; LONG-TERM EFFICACY; METFORMIN PLUS SULFONYLUREA; INADEQUATE GLYCEMIC CONTROL; DOUBLE-BLIND; ADD-ON; PARALLEL-GROUP; CARDIOVASCULAR OUTCOMES; JAPANESE PATIENTS; DRUG-INTERACTIONS;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
SGLT2 (sodium-glucose cotransporter type 2) inhibitors are a new class of drugs which reversibly block the glucose reabsorption that occurs in the kidneys. Since their mechanisms of action do not rely on insulin secretion, they constitute a complementary alternative to the classic treatment of type 2 diabetes mellitus. A glycemic level reduction in patients who used SGLT2 inhibitors due to the reversible block of their transporters could be observed. Associated with this, there was a reduction in body weight and blood pressure (BP) caused by osmotic diuresis. Few adverse effects and low drug interaction combined with antihyperglycemic effects are some of the benefits of these inhibitors widely discussed in clinical trials. Patients with history of urogenital infections or those on diuretics must be carefully evaluated before the administration of these drugs. While a promising class of drugs indicated as a treatment for patients with type 2 diabetes mellitus, SGLT2 inhibitors should not be prescribed for individuals with severe renal or hepatic impairment. Therefore, as there are only a few situations in which they should not be indicated, the efficacy, safety and tolerability of these inhibitors allow them to be used in a wide range of patients. Nevertheless, further researches are required so that the possible long-term risks can be studied and the benefits associated with their use can be more objectively elucidated.
引用
收藏
页码:199 / 211
页数:13
相关论文
共 78 条
[1]  
[Anonymous], IDF Diabetes Atlas 2021
[2]   Dapagliflozin add-on to metformin in type 2 diabetes inadequately controlled with metformin: a randomized, double-blind, placebo-controlled 102-week trial [J].
Bailey, Clifford J. ;
Gross, Jorge L. ;
Hennicken, Delphine ;
Iqbal, Nayyar ;
Mansfield, Traci A. ;
List, James F. .
BMC MEDICINE, 2013, 11
[3]   Dapagliflozin: Glucuretic action and beyond [J].
Balakumar, Pitchai ;
Sundram, Karupiah ;
Dhanaraj, Sokkalingam A. .
PHARMACOLOGICAL RESEARCH, 2014, 82 :34-39
[4]  
Bhanot S., 2009, Diabetes, V58, pA328
[5]   Long-term efficacy and safety of canagliflozin over 104 weeks in patients aged 55-80 years with type 2 diabetes [J].
Bode, B. ;
Stenlof, K. ;
Harris, S. ;
Sullivan, D. ;
Fung, A. ;
Usiskin, K. ;
Meininger, G. .
DIABETES OBESITY & METABOLISM, 2015, 17 (03) :294-303
[6]   Effects of Dapagliflozin on Body Weight, Total Fat Mass, and Regional Adipose Tissue Distribution in Patients with Type 2 Diabetes Mellitus with Inadequate Glycemic Control on Metformin [J].
Bolinder, Jan ;
Ljunggren, Osten ;
Kullberg, Joel ;
Johansson, Lars ;
Wilding, John ;
Langkilde, Anna Maria ;
Sugg, Jennifer ;
Parikh, Shamik .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2012, 97 (03) :1020-1031
[7]  
CANADIAN AGENCY DRUGS TECHNOLOGIES FOR AND IN HEALTH, 2015, CARD OUTC SOD GLUC C
[8]   Toxigenic and Metabolic Causes of Ketosis and Ketoacidotic Syndromes [J].
Cartwright, Martina M. ;
Hajja, Waddah ;
Al-Khatib, Sofian ;
Hazeghazam, Maryam ;
Sreedhar, Dharmashree ;
Li, Rebecca Na ;
Wong-McKinstry, Edna ;
Carlson, Richard W. .
CRITICAL CARE CLINICS, 2012, 28 (04) :601-+
[9]  
CENTERS FOR DISEASE CONTROL AND PREVENTION, 2014, NAT DIAB STAT REP ES
[10]  
Dagan Amir, 2015, Harefuah, V154, P200