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The regulatory role of DPP4 in atherosclerotic disease
Lihua Duan1,2, Xiaoquan Rao2, Chang Xia2,3
1Department of Rheumatology and Clinical Immunology, The First Affiliated Hospital of Xiamen University, Xiamen, 361003, Fujian, China.
Abstract:
The increasing prevalence of atherosclerosis has become a worldwide health concern. Although significant progress has been made in the understanding of atherosclerosis pathogenesis, the underlying mechanisms are not fully understood. Recent studies suggest dipeptidyl peptidase-4 (DPP4), a regulator of inflammation and metabolism, may be involved in the development of atherosclerotic diseases. There has been increasing clinical and pre-clinical evidence showing DPP4-incretin axis is involved in cardiovascular disease. Although the cardiovascular outcome of DPP4 inhibition or incretin analogues has been or being evaluated by several large scale clinical trials, the exact role of DPP4 in atherosclerotic diseases is not completely understood. In the current review, we will summarize the recent advances in direct and indirect regulatory role of DPP4 in atherosclerosis.
Insights
Dipeptidyl peptidase-4 (DPP4) may play a role in atherosclerosis development and progression. This review summarizes DPP4
Area of Science:
- Cardiovascular Science
- Metabolic Disease Research
- Immunology and Inflammation Studies
Background:
- Atherosclerosis is a growing global health issue with incompletely understood mechanisms.
- Dipeptidyl peptidase-4 (DPP4), a key regulator of inflammation and metabolism, is increasingly implicated in atherosclerotic diseases.
- The DPP4-incretin axis shows emerging links to cardiovascular disease, prompting further investigation.
Purpose of the Study:
- To review recent findings on the direct and indirect roles of DPP4 in atherosclerosis.
- To consolidate current understanding of DPP4's involvement in the pathogenesis of atherosclerotic diseases.
Main Methods:
- Literature review of recent clinical and pre-clinical studies.
- Analysis of research on DPP4 inhibition and incretin analogues in cardiovascular outcomes.
- Synthesis of evidence regarding DPP4's regulatory functions in atherosclerosis.
Main Results:
- DPP4 influences inflammation and metabolism, key factors in atherosclerosis.
- Evidence suggests the DPP4-incretin axis impacts cardiovascular health.
- Ongoing clinical trials are evaluating DPP4 inhibition's cardiovascular effects.
Conclusions:
- DPP4's precise role in atherosclerotic diseases requires further elucidation.
- Understanding DPP4's regulatory functions is crucial for developing novel therapeutic strategies.
- Further research is needed to fully clarify DPP4's complex involvement in atherosclerosis.
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