Thromb Haemost
DOI: 10.1055/a-2754-5302
Review Article

Carotid Plaque Instability and Cerebral Atheroembolism: Future Directions in Stroke-Prevention

Authors

  • Ulf Hedin

    1   Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden
    2   Department of Vascular Surgery and MedTechLabs, Karolinska University Hospital, Stockholm, Sweden
  • Eva Karlöf

    1   Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden
    2   Department of Vascular Surgery and MedTechLabs, Karolinska University Hospital, Stockholm, Sweden

Funding Information Project funding was obtained from the Swedish Heart-Lung Foundation (20180036, 20200531, and 20230447), the Swedish Research Council (2017-01070 and 2021-01516), Karolinska Institutet, King Gustav Vth and Queen Victoria's Foundation, and MedTechLabs.


Graphical Abstract

Abstract

Ischemic stroke affects more than 15 million people annually, where atheroembolism from unstable atherosclerotic plaques in the carotid bifurcation contributes a significant and potentially preventable aetiology. Landmark carotid endarterectomy trials conducted decades ago proved that removing high-grade symptomatic stenoses outperforms medical therapy, yet accurately identifying unstable plaques, the true embolic source, remains elusive. Consequently, procedural efficacy is modest, and more personalized diagnostic methods are necessary for refined risk stratification and improved stroke prevention. Plaque instability and atheroembolism from rupture of the fibrous cap is driven by an enlargement of the lipid-rich necrotic core, inflammation, neovascularisation, intraplaque haemorrhage, and fibrous-cap thinning. Hypoxia-induced angiogenesis produces fragile neovessels that bleed, generating oxidative stress and further destabilisation. Biomolecules escaping into the circulation from such lesions could flag individuals at imminent risk, but imaging modalities such as magnetic resonance, computed tomography angiography, or ultrasound are necessary to identify lesions at risk. Using these methods, aligning imaging phenotypes with molecular signatures of stability or vulnerability can aid in the development of refined diagnostic methods. Integrating blood-based with quantitative imaging biomarkers and systems-biology modelling promises a personalised diagnostic pipeline to screen for circulating signals of instability to detect individuals at risk, together with noninvasive imaging to localise culprit lesions, creating the basis for tailored surgical or pharmacologic therapy. In this review, we discuss scientific advances in the development of such strategies that possess the potential to sharpen patient selection, reduce unnecessary procedures, and advance precision in stroke prevention.

Note

The authors declare no disclosures except that the parts of the content in this article have previously been included in the doctoral thesis by Eva Karlöf (ISBN 978-91-8016-261-6).




Publication History

Received: 16 June 2025

Accepted after revision: 22 November 2025

Accepted Manuscript online:
25 November 2025

Article published online:
05 December 2025

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