Increased Whole Blood Viscosity Is Associated with the Presence of Digital Ulcers in Systemic Sclerosis: Results from a Cross-Sectional Pilot Study
Autor: | Daniel Cho, Tammy O. Utset, Nadera J. Sweiss, Suncica Volkov, Michael Zeisberg, Lawrence S. Zachary, Timothy B. Niewold, Peter Korsten |
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Jazyk: | angličtina |
Rok vydání: | 2017 |
Předmět: |
030203 arthritis & rheumatology
lcsh:Immunologic diseases. Allergy medicine.medical_specialty Article Subject business.industry Immunology Treatment options Convenience sample Whole blood viscosity 030204 cardiovascular system & hematology Surgery Microcirculation 03 medical and health sciences 0302 clinical medicine Immunology and Microbiology (miscellaneous) Rheumatology clinic Internal medicine Immunology and Allergy Medicine In patient business lcsh:RC581-607 Research Article |
Zdroj: | Autoimmune Diseases, Vol 2017 (2017) Autoimmune Diseases |
ISSN: | 2090-0430 2090-0422 |
Popis: | Objective. To investigate the role of whole blood viscosity in digital ulcer (DU) development in patients with diffuse and limited Systemic sclerosis.Methods. A convenience sample of patients with Systemic sclerosis (SSc) was selected from the adult Rheumatology clinic at the University of Chicago. The study group consisted of patients with SSc (with ulcers present, a history of ulcers, and no ulcers); the control group consisted of matched healthy Rheumatology clinic staff. WBV was measured using a scanning capillary viscometer at different shear rates (1–1000 1/s).Results. Whole blood viscosity as measured by a scanning capillary viscometer was increased in patients with SSc compared to healthy controls (p<0.0001). Additionally, patients with present DU had significantly higher whole blood viscosity when compared to patients with a history of DU and patients with no history of DU (p<0.0001). These findings were most pronounced at lower shear rates between 1 and 10 1/s.Conclusion. Whole blood viscosity might be a contributing factor in DU development in patients with SSc. Further studies with larger patient cohorts are required to fully evaluate how increased WBV contributes to the development of DU and whether the currently available treatment options improve the microcirculation by influencing WBV. |
Databáze: | OpenAIRE |
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