Incretin-based medications (GLP-1 receptor agonists, DPP-4 inhibitors) as a means to avoid hypoglycaemic episodes

被引:14
|
作者
Farngren, Johan [1 ]
Ahren, Bo [1 ]
机构
[1] Lund Univ, Dept Clin Sci Lund, BMC C11,Solvegatan 19, S-22184 Lund, Sweden
来源
关键词
Incretin therapy; DPP-4; inhibitors; GLP-1 receptor agonists; Hypoglycaemia; Type; 2; diabetes; TYPE-2; DIABETES-MELLITUS; GLUCOSE-LOWERING DRUGS; DOUBLE-BLIND; CARDIOVASCULAR OUTCOMES; INSULIN-SECRETION; HORMONE RESPONSES; GLUCAGON-RESPONSE; OLDER PATIENTS; PLACEBO; LIRAGLUTIDE;
D O I
10.1016/j.metabol.2019.06.016
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Hypoglycaemia is common in both type 1 and type 2 diabetes and has both acute and long-term consequences. Therefore, a key to proper glucose-lowering therapy in diabetes is to avoid or prevent hypoglycaemia. Incretin therapy (DPP-4 inhibitors and GLP-1 receptor agonists) offers an advantage in this respect, because it reduces glucose with a low risk of hypoglycaemia, both in monotherapy and in combination with other therapies. The reason for this low risk of hypoglycaemia is the glucose dependency of action of incretin therapy and the sustainment of glucose counter-regulatory hormone responses to hypoglycaemia, in particular the glucagon response. Incretin therapy is also associated with a low risk of hypoglycaemia in patient groups which are especially vulnerable and susceptible for hypoglycaemia, e.g., subjects with renal impairment, elderly subjects and subjects with on-going insulin therapy. This review summarizes how incretin therapy may meet the challenges of hypoglycaemia and suggests that incretin therapy is a therapy of choice to avoid hypoglycaemia, both in the general diabetes population and in subjects with increased risk or vulnerability for hypoglycaemia. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:25 / 31
页数:7
相关论文
共 50 条
  • [41] Cardiovascular Actions of GLP-1 and Incretin-Based Pharmacotherapy
    Avogaro, Angelo
    de Kreutzenberg, Saula Vigili
    Fadini, Gian Paolo
    CURRENT DIABETES REPORTS, 2014, 14 (05)
  • [42] INSULIN IS MOST APPROPRIATE COMPARATOR TO GLP-1 RECEPTOR AGONISTS AND DPP-4 INHIBITORS IN REAL-WORLD CARDIOVASCULAR OUTCOME STUDIES
    Ali, A. K.
    Motsko, S. P.
    VALUE IN HEALTH, 2017, 20 (05) : A311 - A311
  • [43] The risk of major osteoporotic fractures with GLP-1 receptor agonists when compared to DPP-4 inhibitors: A Danish nationwide cohort study
    Al-Mashhadi, Zheer Kejlberg
    Viggers, Rikke
    Fuglsang-Nielsen, Rasmus
    Vestergaard, Peter
    Gregersen, Soren
    Starup-Linde, Jakob
    FRONTIERS IN ENDOCRINOLOGY, 2022, 13
  • [45] DPP-4-Hemmer und GLP-1-Rezeptor-AgonistenKardiovaskuläre Effekte DPP-4 inhibitors and GLP-1 receptor agonistsCardiovascular effects
    M. A. Nauck
    M. S. Abd El Aziz
    J. J. Meier
    Der Diabetologe, 2016, 12 : 184 - 194
  • [47] Comparative Effectiveness of SGLT-2 Inhibitors, DPP-4 Inhibitors, and GLP-1 Agonists in US Veterans with and Without CKD
    Narasaki, Yoko
    Kovesdy, Csaba P.
    You, Amy S.
    Potukuchi, Praveen Kumar
    Dashputre, Ankur A.
    Sumida, Keiichi
    Thomas, Fridtjof
    Streja, Elani
    Kalantar-Zadeh, Kamyar
    Rhee, Connie
    JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2021, 32 (10): : 264 - 264
  • [48] SGLT-2 inhibitors were not linked to severe or nonsevere UTIs vs DPP-4 inhibitors or GLP-1 agonists
    Davidson, Mayer B.
    ANNALS OF INTERNAL MEDICINE, 2019, 171 (12) : JC70 - JC70
  • [49] Blood Pressure-Lowering Effect of Newer Antihyperglycemic Agents (SGLT-2 Inhibitors, GLP-1 Receptor Agonists, and DPP-4 Inhibitors)
    Charalampos I. Liakos
    Dimitrios P. Papadopoulos
    Elias A. Sanidas
    Maria I. Markou
    Erifili E. Hatziagelaki
    Charalampos A. Grassos
    Maria L. Velliou
    John D. Barbetseas
    American Journal of Cardiovascular Drugs, 2021, 21 : 123 - 137
  • [50] Blood Pressure-Lowering Effect of Newer Antihyperglycemic Agents (SGLT-2 Inhibitors, GLP-1 Receptor Agonists, and DPP-4 Inhibitors)
    Liakos, Charalampos I.
    Papadopoulos, Dimitrios P.
    Sanidas, Elias A.
    Markou, Maria I.
    Hatziagelaki, Erifili E.
    Grassos, Charalampos A.
    Velliou, Maria L.
    Barbetseas, John D.
    AMERICAN JOURNAL OF CARDIOVASCULAR DRUGS, 2021, 21 (02) : 123 - 137