# Insulin Resistance and Platelet Hyperactivity: Hematological Insights and Nutritional Strategies for Vascular Protection

**Authors:** Kiana Mohammadian, Narges Basirian, Fatemeh Fakhar, Shayan Keramat, Agata Stanek

PMC · DOI: 10.3390/nu18050763 · Nutrients · 2026-02-26

## TL;DR

This paper reviews how insulin resistance increases platelet activity and vascular risks, and how nutrition can help reduce these effects in people with type 2 diabetes.

## Contribution

The paper provides a synthesis of mechanisms linking insulin resistance to platelet dysfunction and highlights novel nutritional strategies for vascular protection.

## Key findings

- Insulin-resistant platelets show increased activation and reduced inhibitory responses, contributing to thrombotic risk.
- Nutritional interventions like Mediterranean diets and bioactive compounds reduce platelet aggregation and inflammation.
- Dietary strategies improve endothelial function and stabilize atherosclerotic plaques in insulin-resistant individuals.

## Abstract

Insulin resistance (IR) promotes a prothrombotic milieu by enhancing platelet hyperactivity, oxidative stress, and endothelial dysfunction, driving both microvascular and macrovascular complications in type 2 diabetes. Our review synthesizes mechanistic evidence showing that insulin-resistant platelets exhibit increased basal activation, elevated sensitivity to agonists, and reduced responsiveness to inhibitory signals, with distinct pro-aggregatory subpopulations amplifying thrombotic risk. Molecular pathways underlying platelet hyperactivation include reactive oxygen species accumulation, advanced glycation end-product signaling, disrupted calcium homeostasis, and impaired nitric oxide/prostacyclin pathways. Clinically, these mechanisms contribute to heightened arterial thrombosis, coronary artery disease, stroke, and microvascular injury, including nephropathy and retinopathy. Nutritional interventions emerge as effective modulators of platelet function and vascular health. Diets such as the Mediterranean, DASH, low-glycemic-index, and plant-based regimens, alongside bioactive compounds—including omega-3 fatty acids, polyphenols, vitamins D, E, C, and minerals like magnesium and zinc—may reduce platelet aggregation, oxidative stress, and systemic inflammation while restoring endothelial function. Clinical and epidemiological evidence demonstrates improvements in flow-mediated dilation, arterial elasticity, and stabilization of atherosclerotic plaques following dietary interventions. Integrating whole-diet strategies with targeted nutrients provides synergistic benefits, suggesting that personalized nutritional approaches can mitigate IR-induced platelet hyperactivity and lower vascular risk. These findings highlight nutrition as a practical, evidence-based adjunct to pharmacotherapy for cardiovascular protection in insulin-resistant populations.

## Linked entities

- **Chemicals:** omega-3 fatty acids (PubChem CID 56842239), vitamin E (PubChem CID 14985), vitamin C (PubChem CID 54670067), magnesium (PubChem CID 5462224), zinc (PubChem CID 23994)
- **Diseases:** type 2 diabetes (MONDO:0005148), coronary artery disease (MONDO:0005010), stroke (MONDO:0005098), retinopathy (MONDO:0005283)

## Full-text entities

- **Genes:** INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}
- **Diseases:** coronary artery disease (MESH:D003324), microvascular injury (MESH:D017566), retinopathy (MESH:D058437), nephropathy (MESH:D007674), type 2 diabetes (MESH:D003924), Platelet Hyperactivity (MESH:D001791), IR (MESH:D007333), stroke (MESH:D020521), endothelial dysfunction (MESH:D014652), inflammation (MESH:D007249), thrombosis (MESH:D013927), atherosclerotic plaques (MESH:D058226)
- **Chemicals:** zinc (MESH:D015032), prostacyclin (MESH:D011464), vitamins D, E, C (-), nitric oxide (MESH:D009569), calcium (MESH:D002118), polyphenols (MESH:D059808), omega-3 fatty acids (MESH:D015525), reactive oxygen species (MESH:D017382), magnesium (MESH:D008274)

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12987119/full.md

## References

97 references — full list in the complete paper: https://tomesphere.com/paper/PMC12987119/full.md

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Source: https://tomesphere.com/paper/PMC12987119