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Haemorheological profile in patients with systemic sclerosis
Amparo Vayá1, José Todolí, Javier Calvo
1Haemorheology and Thrombosis Unit, Department of Clinical Pathology, La Fe University Hospital, Valencia, Spain. vaya_amp@gva.es
Systemic sclerosis (SSc) patients exhibit altered blood rheology, including higher plasma viscosity and erythrocyte aggregation, and reduced erythrocyte deformability. These changes correlate with inflammation markers and may impact microcirculation.
Area of Science:
- Rheology
- Hematology
- Systemic Sclerosis
Background:
- The rheological alterations in systemic sclerosis (SSc) are not well-established.
- Understanding blood flow properties is crucial for SSc pathogenesis and treatment.
Purpose of the Study:
- To comprehensively evaluate the rheological profile in SSc patients.
- To investigate the relationship between rheological parameters, inflammation, and clinical markers in SSc.
Main Methods:
- Compared rheological parameters (blood viscosity, plasma viscosity, erythrocyte aggregation, erythrocyte deformability) in 27 SSc patients and controls.
- Assessed inflammatory markers (fibrinogen, CRP), lipids, and erythrocyte indices.
- Correlated rheological findings with inflammation markers and autoantibodies.
Main Results:
- SSc patients demonstrated significantly higher fibrinogen, plasma viscosity, and erythrocyte aggregation (P<0.01).
- Erythrocyte deformability was significantly lower in SSc patients (P<0.01).
- Reduced erythrocyte deformability correlated negatively with inflammation markers (CRP, fibrinogen) and was lower in patients with anticentromere antibodies.
Conclusions:
- Systemic sclerosis is associated with significant rheological disturbances, characterized by increased viscosity and aggregation, and impaired deformability.
- Decreased erythrocyte deformability appears linked to inflammatory processes and may be influenced by specific autoantibodies in SSc.
- Further research is needed to elucidate the clinical significance of these rheological findings in SSc.
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