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Departments of 1 Internal Medicine, 3 Cardiology, and 4 Hematology, Sourasky Medical Center, 64239 Tel-Aviv; and 2 Department of Biochemistry, Hebrew University-Hadassah Medical School, Jerusalem 91120, Israel
To identify clinically relevant
parameters of red blood cell (RBC) aggregation, we examined
correlations of aggregation parameters with C-reactive protein and
fibrinogen in unstable angina (UA), acute myocardial infarction (AMI),
and bacterial infection (BI). Aggregation parameters were derived from
the distribution of RBC population into aggregate sizes (cells per
aggregate) and changing of the distribution by flow-derived
shear stress. Increased aggregation was observed in the following
order: UA, AMI, and BI. The best correlation was obtained by
integration of large aggregate fraction as a function of shear stress.
To differentiate plasmatic from cellular factors in RBC aggregation, we
determined the aggregation in the presence and absence of plasma
and formulated a "plasma factor" (PF) ranging from 0 to 1. In AMI the enhanced aggregation was entirely due to PF (PF = 1),
whereas in UA and BI it was due to both plasmatic and cellular factors
(0
PF
1). It is proposed that clinically
relevant parameters of RBC aggregation should express both RBC
aggregate size distribution and aggregate resistance to disaggregation
and distinguish between plasmatic and cellular factors.
acute-phase response; aggregate size distribution; shear stress
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