Red blood cell distribution width is associated with increased interactions of blood cells with vascular wall

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作者
Sharan Ananthaseshan
Krzysztof Bojakowski
Mariusz Sacharczuk
Piotr Poznanski
Dominik S. Skiba
Lisa Prahl Wittberg
Jordan McKenzie
Anna Szkulmowska
Niclas Berg
Piotr Andziak
Hanna Menkens
Maciej Wojtkowski
Dorota Religa
Fredrik Lundell
Tomasz Guzik
Zbigniew Gaciong
Piotr Religa
机构
[1] Karolinska Institute,Department of Medicine, Solna
[2] Medical University of Warsaw,Department of Internal Medicine, Hypertension and Vascular Diseases
[3] Centre of Postgraduate Medical Education,2nd Vascular Surgery and Angiology Department
[4] Polish Academy of Sciences,Department of Experimental Genomics, Institute of Genetics and Animal Biotechnology
[5] Royal Institute of Technology,KTH Mechanics
[6] AM2M Ltd. L.P.,Institute of Physics
[7] Nicolaus Copernicus University,NVS
[8] Karolinska Institute,Institute of Cardiovascular and Medical Sciences
[9] University of Glasgow,undefined
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The mechanism underlying the association between elevated red cell distribution width (RDW) and poor prognosis in variety of diseases is unknown although many researchers consider RDW a marker of inflammation. We hypothesized that RDW directly affects intravascular hemodynamics, interactions between circulating cells and vessel wall, inducing local changes predisposing to atherothrombosis. We applied different human and animal models to verify our hypothesis. Carotid plaques harvested from patients with high RDW had increased expression of genes and proteins associated with accelerated atherosclerosis as compared to subjects with low RDW. In microfluidic channels samples of blood from high RDW subjects showed flow pattern facilitating direct interaction with vessel wall. Flow pattern was also dependent on RDW value in mouse carotid arteries analyzed with Magnetic Resonance Imaging. In different mouse models of elevated RDW accelerated development of atherosclerotic lesions in aortas was observed. Therefore, comprehensive biological, fluid physics and optics studies showed that variation of red blood cells size measured by RDW results in increased interactions between vascular wall and circulating morphotic elements which contribute to vascular pathology.
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