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Fibrinaloid Microclots-Induced Microcirculation Dysfunction: Mechanism and Laser-Based Haemodynamic Validation

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Fibrinaloid Microclots-Induced Microcirculation Dysfunction: Mechanism and Laser-Based Haemodynamic Validation

Author Information
1
Department of Biochemistry, Cell and Systems Biology, Institute of Systems, Molecular and Integrative Biology, Faculty of Health and Life Sciences, University of Liverpool, Crown St, Liverpool L69 7ZB, UK
2
Department of Physiological Sciences, Faculty of Science, Stellenbosch University, Stellenbosch Private Bag X1 Matieland, Stellenbosch 7602, South Africa
3
School of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing 10026, China
4
Institute of Ethnic Medicine and Pharmacy, Beijing University of Chinese Medicine, Beijing 10026, China
*
Authors to whom correspondence should be addressed.

Received: 23 January 2026 Revised: 20 March 2026 Accepted: 15 April 2026 Published: 09 May 2026

Creative Commons

© 2026 The authors. This is an open access article under the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/).

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Cardiovasc. Sci. 2026, 3(2), 10005; DOI: 10.70322/cvs.2026.10005
ABSTRACT: The microcirculation typically refers to those capillaries less than 100 μm in diameter. We have shown that blood can clot into an anomalous amyloid form, manifesting as microclots of typically 2–200 μm equivalent diameter that are rather resistant to fibrinolysis. Because they contain fibrin and other proteins in an amyloid form, we have referred to them as fibrinaloid microclot complexes. We have also previously developed the idea that endothelial dysfunction can both lead to and be caused by the fibrinaloid microclots so formed, such that this can slow or block entirely parts of the microcirculation. The microclots might be thought of as a ‘structural’ manifestation in that they are actual, observable structures. This impairment of the microcirculation is referred to in Traditional Chinese Medicine (TCM) as ‘blood stasis’. It is thus desirable to have ‘functional’ methods that can measure these effects on the microcirculation directly. As a complement to a recent survey of nailfold capillaroscopy, the present paper provides a wide-ranging review of the utility of laser speckle imaging (LSI) and laser Doppler imaging (LDI) for assessing the microcirculation in a large variety of diseases in which it is considered to be involved. These include Long COVID, sepsis, and ischaemic stroke. In all cases in which fibrinaloid microclots have been observed, so too do these methods detect an impairment of the microcirculation. Notably, blood pressure is raised while blood flow in the microcirculation is lower; this clearly speaks to occlusion and/or capillary rarefaction, and indicates that the raised blood pressure is the effect and not the cause of the decrease in flow rate or stasis of the microcirculation. As rapid, information-rich and non-invasive methods, LSI and LDI seem to have outstanding potential for assessing the role of fibrinaloid microclots in affecting blood stasis in the microcirculation, in a huge variety of inflammatory diseases and syndromes.
Keywords: Clotting; Amyloid; Fibrinaloid; Laser-doppler imaging; Laser speckle imaging; Cross-seeding; Fibrils; Microcirculation
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