We studied glycocalicin (GC), expressed as plasma GC concentration and
as GC index (ratio to platelet count), in 129 thrombocytopenic patien
ts (platelet count < 100x10(9)/l) and 60 sex- and age-matched controls
. Seventy-two patients had idiopathic immune thrombocytopenia, 32 seco
ndary immune thrombocytopenia, 8 microangiopathic thrombocytopenia and
17 thrombocytopenia secondary to bone marrow aplasia. Patients with i
mmune thrombocytopenia (ITP) were also subclassified, according to the
ir clinical behaviour, as having active disease or being in spontaneou
s or therapy-induced partial remission. A significant correlation was
found between glycocalicin levels and platelet count both in normals a
nd in patients with bone marrow aplasia (r=0.75). ITP patients showed
a GC index significantly higher than controls (6.02+/-7.87 vs. 0.9+/-0
.2, p<0.001). When ITP patients with similar platelet count (30-50x10(
9)/l) were studied, the mean level of GC and the GC index were signifi
cantly higher in those patients with active disease than in those in r
emission (0.97+/-0.38 vs. 0.58+/-0.17 mu g/ml, p<0.05; 6.41+/-2.64 vs.
3.44+/-0.94, p<0.05, respectively). A longitudinal study performed in
10 patients with different subtypes of ITP suggested a positive corre
lation between GC index and the activity of the disease. The GC value
and GC index were significantly higher in patients with microangiopath
ic thrombocytopenia than in controls (1.44+/-0.73 vs. 0.8+/-0.16 mu g/
ml, p<0.01; and 18.77+/-22.23 vs. 0.9+/-0.2, p<0.001, respectively). T
he GC value was significantly lower in bone marrow failure (0.15+/-0.0
4 mu g/ml, p<0.01) compared to controls, while no difference was obser
ved in the GC index. Our data confirm that the GC index is helpful in
differentiating thrombocytopenia due to increased platelet destruction
from the one due to impaired production. In addition, the assay has b
een proven useful in the differential diagnosis of different ITP subty
pes and their follow-up.