Increased Whole Blood Viscosity Is Associated with the Presence of Digital Ulcers in Systemic Sclerosis: Results from a Cross-Sectional Pilot Study

Author:

Korsten Peter1ORCID,Niewold Timothy B.2ORCID,Zeisberg Michael1,Utset Tammy O.3,Cho Daniel4,Zachary Lawrence S.5,Sweiss Nadera J.67,Volkov Suncica6

Affiliation:

1. Department of Nephrology and Rheumatology, University Medical Center Goettingen, Goettingen, Germany

2. Division of Rheumatology and Department of Immunology, Mayo Clinic, Rochester, MN, USA

3. Department of Rheumatology, University of Chicago, Chicago, IL, USA

4. Rheovector LLC, King of Prussia, PA, USA

5. Section of Plastic and Reconstructive Surgery, Department of Surgery, University of Chicago, Chicago, IL, USA

6. Division of Rheumatology, University of Illinois at Chicago, Chicago, IL, USA

7. Division of Pulmonary, Critical Care, Sleep and Allergy, University of Illinois at Chicago, Chicago, IL, USA

Abstract

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.

Publisher

Hindawi Limited

Subject

Immunology and Microbiology (miscellaneous),Immunology,Immunology and Allergy

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