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Preparation of Washed Human Platelets for Quantitative Metabolic Flux Studies
Published on: January 10, 2025
Platelet perturbations in diabetes: implications for cardiovascular disease risk and treatment
Shiny Mathewkutty1, Darren K McGuire
1Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Insights
Type 2 diabetes mellitus (DM) increases cardiovascular disease (CVD) risk. Improving antiplatelet therapies offers a promising strategy to reduce residual CVD risk in patients with DM.
Area of Science:
- Cardiology
- Endocrinology
- Pharmacology
Background:
- Type 2 diabetes mellitus (DM) prevalence is rising globally, leading to increased cardiovascular disease (CVD) complications.
- Despite advancements in evidence-based therapies, a residual CVD risk persists in patients with DM.
- Platelet function is significantly altered in DM, suggesting potential benefits from improved antiplatelet strategies.
Purpose of the Study:
- To explore the potential of enhanced antiplatelet therapies in mitigating residual cardiovascular disease risk in patients with Type 2 diabetes mellitus.
Main Methods:
- Review of ex vivo platelet function assessments in diabetic patients.
- Analysis of clinical outcomes trials evaluating antiplatelet agents in high-risk populations.
Main Results:
- Emerging data suggest that perturbations in platelet function associated with DM contribute to residual cardiovascular risk.
- Clinical outcomes trials provide preliminary support for the efficacy of certain antiplatelet approaches in this cohort.
Conclusions:
- Optimizing antiplatelet therapies represents a key opportunity for clinical advancement in managing cardiovascular risk in Type 2 diabetes mellitus.
- Further research and development in antiplatelet strategies are warranted for this vulnerable patient population.
Abstract:
The prevalence of Type 2 diabetes mellitus (DM) continues to increase globally and brings with it a parallel increase in the associated cardiovascular disease complications. Despite advances in evidence-based therapies for cardiovascular disease risk modification, many of which are especially effective among patients with DM, there remains a residual degree of cardiovascular disease risk associated with DM, yielding opportunity for continued clinical advances. Given the myriad perturbations of platelet function associated with DM, improvements in antiplatelet therapies hold particular promise for this high-risk population of patients, with emerging data from ex vivo assessments and clinical outcomes trials providing a basis of support for this concept.
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