Table 2.

Relationships between the levels of individual hemostatic markers and presence of phosphatidylserine-positive erythrocytes and platelets in patients with sickle cell disease

MarkerRed cellPlatelet
RPRP
F1.2 .521 < .0002 −.125 > .35 
TAT .244 > .09 −.080 > .55 
D-dimer .629 < .000002 −.087 > .55 
PAP .372 < .01 .015 > .90 
tPA .028 > .85 .045 > .75 
PAI-1 .241 > .09 .189 > .15 
MarkerRed cellPlatelet
RPRP
F1.2 .521 < .0002 −.125 > .35 
TAT .244 > .09 −.080 > .55 
D-dimer .629 < .000002 −.087 > .55 
PAP .372 < .01 .015 > .90 
tPA .028 > .85 .045 > .75 
PAI-1 .241 > .09 .189 > .15 

TAT indicates thrombin-antithrombin; PAP, plasmin-antiplasmin; tPA, tissue plasminogen activator, PAI-1, plasminogen activator inhibitor-1.

Plasma levels of hemostatic markers were evaluated by using commercially available enzyme-linked immunosorbent assay kits, and circulating levels of phosphatidylserine-positive erythrocytes and platelets were assessed by using annexin V by flow cytometry. Values presented for the R and P values were obtained by using the Pearson test on log-transformed data. Similar results were obtained by using the Spearman test on rank-transformed data.

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