The Emerging Role of Dual GLP-1 and GIP Receptor Agonists in Glycemic Management and Cardiovascular Risk Reduction

被引:31
|
作者
Rizvi, Ali A. [1 ]
Rizzo, Manfredi [2 ]
机构
[1] Univ Cent Florida, Dept Med, Coll Med, 3400 Quadrangle Blvd, Orlando, FL 32817 USA
[2] Univ Palermo, Dept Hlth Promot Mother & Child Care, Internal Med & Med Specialties Promise, Palermo, Italy
来源
DIABETES METABOLIC SYNDROME AND OBESITY-TARGETS AND THERAPY | 2022年 / 15卷
关键词
type; 2; diabetes; incretins; glucagon-like peptide-1; glucose-dependent insulinotropic polypeptide; DEPENDENT INSULINOTROPIC POLYPEPTIDE; DEFECTIVE AMPLIFICATION; DIABETES-MELLITUS; GLUCOSE; GLUCAGON; SENSITIVITY; PATHOPHYSIOLOGY; TIRZEPATIDE; PHYSIOLOGY; OBESITY;
D O I
10.2147/DMSO.S351982
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The incretin pathway is a self-regulating feedback system connecting the gut with the brain, pancreas, and liver. Its predominant action is on the postprandial glucose levels, with extraglycemic effects on fat metabolism and endovascular function. Of the two main incretin hormones released with food ingestion, the actions of glucagon-like peptide-1 (GLP-1) have been exploited for therapeutic benefit. However, little attention has been paid to glucose-dependent insulinotropic polypeptide (GIP) until the recent experimental introduction of dual agonists, or "twincretins". Interestingly, simultaneous activation of both receptors is not only replicative of normal physiology, it seems to be an innovative way to enhance their mutual salubrious actions. In patients with type 2 diabetes, dual agonists can have powerful benefits for glucose control and weight reduction. Additionally, there is mounting evidence of their favorable cardiovascular impact, making them potentially appealing pharmacologic agents of choice in the future. Although we seem to be poised on the horizons of exciting new breakthroughs, much knowledge has yet to be gained before these novel agents are ready for prime time.
引用
收藏
页码:1023 / 1030
页数:8
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