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Published on: September 26, 2018
Targeting multiple domains of residual cardiovascular disease risk in patients with diabetes
Kershaw V Patel1, Muthiah Vaduganathan2
1Department of Internal Medicine, Division of Cardiology, University of Texas Southwestern Medical Center, Dallas, Texas.
Purpose Of Review:
There has been a recent resurgence of diabetes-related cardiovascular complications after years of steady improvement. This review highlights established and emerging contemporary secondary prevention approaches that lower the risk of atherosclerotic and nonatherosclerotic cardiovascular disease events among patients with diabetes.
Recent Findings:
Secondary prevention therapies modify residual risk targets, including cardiometabolic pathways, lipoproteins, thrombosis, and inflammation. Large-scale clinical trials of sodium-glucose cotransporter-2 inhibitors have demonstrated significant reductions in hospitalization for heart failure. Glucagon-like peptide-1 receptor agonists have reduced the risk of major adverse cardiovascular events. Recent clinical trials provide evidence supporting the use of nonstatin lipid-lowering therapies, novel antiplatelet and anticoagulant strategies, and antiinflammatory strategies in select cases.
Summary:
Therapeutic approaches targeting multiple distinct pathways have been shown to improve cardiometabolic risk in diabetes. Individual patient characteristics and consideration of residual risk targets may help guide selection of comprehensive secondary prevention approaches.
Insights
Recent advances in diabetes care offer new ways to prevent heart disease. Treatments targeting multiple pathways significantly reduce cardiovascular risks in patients with diabetes.
Area of Science:
- Cardiology
- Endocrinology
- Pharmacology
Background:
- Diabetes mellitus is associated with a significant increase in cardiovascular disease (CVD) risk.
- Despite previous improvements, a resurgence in diabetes-related CVD complications is currently observed.
- Secondary prevention strategies are crucial for managing residual cardiovascular risk in diabetic patients.
Purpose of the Study:
- To review established and emerging secondary prevention strategies for CVD in patients with diabetes.
- To highlight contemporary approaches that mitigate atherosclerotic and nonatherosclerotic CVD events.
- To discuss therapeutic targets including cardiometabolic pathways, lipoproteins, thrombosis, and inflammation.
Main Methods:
- Review of large-scale clinical trials and recent evidence.
- Analysis of pharmacological interventions including sodium-glucose cotransporter-2 inhibitors and glucagon-like peptide-1 receptor agonists.
- Evaluation of nonstatin lipid-lowering therapies, antiplatelet and anticoagulant strategies, and anti-inflammatory agents.
Main Results:
- Sodium-glucose cotransporter-2 inhibitors significantly reduce heart failure hospitalizations.
- Glucagon-like peptide-1 receptor agonists decrease the risk of major adverse cardiovascular events.
- Emerging evidence supports novel lipid-lowering, antiplatelet, anticoagulant, and anti-inflammatory therapies in select patients.
Conclusions:
- Multifaceted therapeutic approaches targeting distinct pathways improve cardiometabolic risk in diabetes.
- Individual patient characteristics and residual risk targets guide the selection of comprehensive secondary prevention.
- Optimizing secondary prevention is key to addressing the resurgence of cardiovascular complications in diabetes.
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