# Cardiovascular Disease and Diabetes: A New Challenge in the Treatment and Management

**Authors:** Graziano Riccioni, Chiara Notarangelo, Mario Riccioni, Nicolantonio D’Orazio

PMC · DOI: 10.3390/ijms27010354 · International Journal of Molecular Sciences · 2025-12-29

## TL;DR

This paper reviews new diabetes drugs that effectively manage blood sugar and reduce cardiovascular risks in diabetic patients.

## Contribution

The paper summarizes the clinical efficacy of novel glucose-lowering agents in treating diabetes with cardiovascular benefits.

## Key findings

- New glucose-lowering drugs show similar effectiveness to traditional antidiabetic drugs.
- These drugs have excellent cardiovascular safety and reduce major cardiovascular events.
- They are particularly beneficial in the early phase of diabetic disease.

## Abstract

Cardiovascular diseases (CVDs) represent one of the leading causes of morbidity and mortality in patients with diabetes. However, a correct and effective glycaemic control obtained by pharmacologic interventions, such as the use the novel glucose-lowering agents, demonstrated efficacy in reducing the risk of both cardiovascular events and mortality. The latest classes of glucose-lowering drugs introduced in the clinical practice are DPP4 inhibitors (sitagliptin, saxagliptin, vildagliptin, linagliptin, and alogliptin), GLP-1 receptor agonists (semaglutide, liraglutide, albiglutide, dulaglutide, exenatide, and lixenatide), and SGLT-2 inhibitors (empaglifozin, canaglifozin, and dapaglifozin). Multiple lines of evidence show that all these new drugs associated with the treatment of diabetic disease have the same effectiveness as the traditional antidiabetic drugs, and excellent cardiovascular safety, highlighting their potential in significantly reducing major cardiovascular events and mortality. The aim of our review is to summarise the clinical efficacy of these recently introduced drugs to optimise treatment strategies, especially in the early phase of diabetic disease.

## Linked entities

- **Chemicals:** sitagliptin (PubChem CID 4369359), saxagliptin (PubChem CID 11243969), vildagliptin (PubChem CID 6918537), linagliptin (PubChem CID 10096344), alogliptin (PubChem CID 11450633), semaglutide (PubChem CID 56843331), liraglutide (PubChem CID 16134956), albiglutide (PubChem CID 122173812), exenatide (PubChem CID 45588096)
- **Diseases:** diabetes (MONDO:0005015)

## Full-text entities

- **Diseases:** Diabetes (MESH:D003920), CVDs (MESH:D002318)
- **Chemicals:** sitagliptin (MESH:D000068900), canaglifozin (-), saxagliptin (MESH:C502994), vildagliptin (MESH:D000077597), linagliptin (MESH:D000069476), alogliptin (MESH:C520853), exenatide (MESH:D000077270)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

68 references — full list in the complete paper: https://tomesphere.com/paper/PMC12785618/full.md

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Source: https://tomesphere.com/paper/PMC12785618