Literature DB >> 24943305

Beyond glycemic control: cardiovascular effects of incretin-based therapies.

Franca S Angeli1, Richard P Shannon.   

Abstract

As cardiovascular (CV) disease remains the major cause of mortality and morbidity in type 2 diabetes mellitus, reducing macrovascular complications has been a major target of antiglycemic therapies. Emerging evidence suggests that incretin-based therapies are safe and may provide CV and cerebrovascular (CBV) benefits beyond those attributable to glycemic control, making the class an attractive therapeutic option. However, the mechanisms whereby the various classes of incretin-based therapies exert CV and CBV benefits may be distinct and may not necessarily lead to similar outcomes. In this chapter, we will discuss the potential mechanisms and current understanding of CV and CBV benefits of native glucagon-like peptide (GLP)-1, GLP-1 receptor agonists and analogues, and of dipeptidyl peptidase-4 inhibitor therapies as a means to better understand differences in safety and efficacy.
© 2014 S. Karger AG, Basel.

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Year:  2014        PMID: 24943305     DOI: 10.1159/000360598

Source DB:  PubMed          Journal:  Front Horm Res        ISSN: 0301-3073            Impact factor:   2.606


  3 in total

1.  Letter: economic impact of combining metformin with dipeptidyl peptidase-4 inhibitors in diabetic patients with renal impairment in spanish patients (diabetes metab j 2015;39:74-81).

Authors:  Hannah Seok
Journal:  Diabetes Metab J       Date:  2015-04       Impact factor: 5.376

2.  Liraglutide attenuates high glucose-induced abnormal cell migration, proliferation, and apoptosis of vascular smooth muscle cells by activating the GLP-1 receptor, and inhibiting ERK1/2 and PI3K/Akt signaling pathways.

Authors:  Lili Shi; Ye Ji; Xiaoyan Jiang; Lihong Zhou; Ying Xu; Yanbo Li; Wei Jiang; Ping Meng; Xiaomin Liu
Journal:  Cardiovasc Diabetol       Date:  2015-02-07       Impact factor: 9.951

3.  Glucagon-like peptide-1 receptor agonist reduces di(2-ethylhexyl) phthalate-induced atherosclerotic processes in vascular smooth muscle cells.

Authors:  Jin Hee Kim
Journal:  Physiol Res       Date:  2020-11-02       Impact factor: 1.881

  3 in total

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