3P-0660 Blood electrical impedance closely matches whole blood viscosity as useful inflammation marker linked to red blood cell aggregation

2003 ◽  
Vol 4 (2) ◽  
pp. 207
Author(s):  
G. Pop ◽  
W. Hop ◽  
L. Moraru ◽  
J. Quak ◽  
D. Dekkers ◽  
...  
2003 ◽  
Vol 13 (6) ◽  
pp. 305-312 ◽  
Author(s):  
G.A.M. Pop ◽  
W.J. Hop ◽  
L. Moraru ◽  
M. van der Jagt ◽  
J. Quak ◽  
...  

AbstractRed blood cell aggregation (RBCa) is a sensitive inflammation marker. RBCa determination from erythrocyte sedimentation rate, ESR, is used since long, but is unspecific unless corrected for hematocrit, Ht. Whole blood viscosity measurement at low shear rate is also sensitive to RBCa but is cumbersome to apply. To investigate whether electrical blood impedance, being sensitive to spatial red cell distribution, can be a good alternative to determine RBCa in low shear conditions. Blood was collected from 7 healthy volunteers. From each 16 different samples were prepared with 4 different Ht’s and with 4 different fibrinogen concentrations. Viscosity was measured at low shear rate (4.04 s-1) with a rotational viscometer at 37˚C. Electrical blood impedance was measured during similar shear conditions and temperature in a specially designed cuvette. ESR was determined according to Westergren. A logarithmic increase of viscosity as well as of capacitance, Cm, is seen when fibrinogen rises and an exponential increase when Ht rises. However, ESR shows a logarithmic decrease with increasing Ht and an exponential increase when fibrinogen rises. The viscosity could be accurately described using an exponential model. Under similar low shear conditions and temperature in-vitro, either whole blood viscosity or electrical blood capacitance reflect red blood cell aggregation due to fibrinogen and Ht variation in a similar way.


Author(s):  
Elie Nader ◽  
Christophe Nougier ◽  
Camille Boisson ◽  
Solene Poutrel ◽  
Judith Catella ◽  
...  

2013 ◽  
Vol 12 (5) ◽  
pp. 5-12
Author(s):  
M. N. Azhermacheva ◽  
D. M. Plotnikov ◽  
O. I. Aliev ◽  
V. M. Alifirova ◽  
M. B. Plotnikov ◽  
...  

The study evaluated the rheological parameters of blood: blood viscosity, plasma viscosity, hematocrit, red blood cell aggregation and deformability. The severity of the patients was assessed by clinical scales:Glasgowcoma scale, the scale NIHSS, Barthel index. The study found that in the acute phase of ischemic stroke increased blood viscosity by increasing red blood cell aggregation and reduced erythrocyte deformability. The increase in the viscosity of the blood in acute ischemic stroke is accompanied by increased severity of neurological disorders.


2012 ◽  
Vol 87 (11) ◽  
pp. E129-E129 ◽  
Author(s):  
Nathalie Lemonne ◽  
Philippe Connes ◽  
Marc Romana ◽  
Jens Vent-Schmidt ◽  
Véronique Bourhis ◽  
...  

Metabolites ◽  
2021 ◽  
Vol 11 (12) ◽  
pp. 806
Author(s):  
Katalin Biro ◽  
Gergely Feher ◽  
Judit Vekasi ◽  
Peter Kenyeres ◽  
Kalman Toth ◽  
...  

Diabetes mellitus influences several important hemorheological parameters including blood viscosity, erythrocyte aggregation and deformability. In the present study, 159 type-2 diabetic patients and 25 healthy controls were involved. Patient’s age, body weight, body mass index (BMI), smoking habits, physical activity, history of cardiovascular diseases, current antidiabetic therapy and concomitant medication were recorded. Patients were grouped according to their antidiabetic treatment with insulin, or with one or more of the following antidiabetic drugs: metformin, sulfonylureas, acarbose, or no antidiabetic therapy. Hemorheological measurements (hematocrit, erythrocyte aggregation, plasma fibrinogen, whole blood and plasma viscosity), von Willebrand factor activity, and platelet aggregation measurements were performed. Platelet aggregation was investigated with the method of Born. Plasma viscosity and red blood cell aggregation were significatly higher in diabetes. No significant difference was found in hemorheological parameters between different antidiabetic regimens. Whole blood and plasma viscosity and red blood cell aggregation correlated with glucose levels but not with HbA1C levels. In conclusion, plasma and whole blood viscosity, as well as red blood cell aggregation appear to be associated with concurrent hyperglycemia, but not with the quality of glycemic control or the applied antidiabetic treatment. Platelet aggregation induced by ADP or epinephrine does not seem to be associated with diabetes even at subthreshold doses.


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