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Evaluation of Whole Blood Viscosity in Patients with Aortic Sclerosis
Pınar Türker Duyuler1, Serkan Duyuler2, Mehmet İleri1
1Department of Cardiology, Ankara Numune Training and Research Hospital, Ankara, Turkey.
Insights
Higher whole blood viscosity (WBV) is linked to aortic sclerosis (AS). This study found increased WBV in patients with AS, suggesting it’s an independent predictor of this cardiovascular condition.
Area of Science:
- Cardiology
- Biophysics
Background:
- Blood viscosity and aortic sclerosis (AS) are established cardiovascular event predictors.
- The relationship between blood viscosity and AS requires further investigation.
- This study explores the connection between whole blood viscosity (WBV) and AS.
Purpose of the Study:
- To investigate the potential association between whole blood viscosity (WBV) and aortic sclerosis (AS).
Main Methods:
- Aortic sclerosis (AS) diagnosis via transthoracic echocardiography.
- Whole blood viscosity (WBV) estimated using validated formulas based on hematocrit (HcT) and total protein (TP) at high shear rate (HSR) (208/s) and low shear rate (LSR) (0.5/s).
- Comparison of WBV (HSR and LSR) between patients with and without AS.
Main Results:
- Patients with AS showed significantly higher total protein levels compared to controls.
- Whole blood viscosity (WBV) at both LSR (0.5/s) and HSR (208/s) was significantly higher in the AS group.
- WBV emerged as an independent predictor of AS in multivariate analysis (p < 0.001).
Conclusions:
- Patients with aortic sclerosis exhibit elevated whole blood viscosity (WBV) at both low and high shear rates.
- WBV is independently associated with the presence of aortic sclerosis (AS).
Abstract:
Background: Blood viscosity and aortic sclerosis (AS) are strong predictors of cardiovascular events. The effects of blood viscosity on AS have not been studied adequately. We aimed to investigate the potential connection between whole blood viscosity (WBV) and AS. Methods: AS was detected by transthoracic echocardiography. The estimation of WBV was carried out at both high shear rate (HSR) (208/s) and low shear rate (LSR) (0.5/s) by previously validated formulae using hematocrit (HcT) and total protein (TP) in g/L. WBV at HSR (208/s) is: (0.12 × HcT) + 0.17 (TP - 2.07) and WBV at LSR (0.5/s) is: (1.89 × HcT) + 3.76 (TP - 78.42). Comparisons of WBV at both HSR and LSR were made between patients with and without AS. Results: We included 94 patients with AS (male = 30.9%, mean age = 67.5 y) and 97 control subjects without AS (male =26.6%, mean age = 69.1 y). Almost all of the clinical, echocardiographic, and biochemical characteristics were similar, but TP values were significantly higher in the AS group than in the control group (72.9 ± 5 g/L vs. 75.8 ± 6.1 g/L; p value < 0.001). Hemoglobin and HcT levels were similar (p value = 0.604 and p value = 0.431, respectively). In the AS group, WBV at LSR and HSR was higher than that in the control group (p value = 0.001 for both LSR and HSR). In multiple stepwise logistic regression analysis, WBV was an independent predictor of AS (p value < 0.001). Conclusion: We found higher WBV in patients with AS than in patients without AS at both LSR (0.5/s) and HSR (208/s). WBV at both LSR and HSR was independently associated with AS.
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