Increased levels of the soluble adhesion molecule E‐selectin in patients with chronic myeloproliferative disorders and thromboembolic complications
Patients with chronic myeloproliferative disorders (CMD) show a high frequency of thrombosis. For this reason we evaluated endothelial cell markers, soluble adhesion molecule E‐selectin (sELAM), and thrombomodulin (TM) in 25 patients with CMD. Among them nine presented thromboses in their past histo...
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Published in | American journal of hematology Vol. 57; no. 2; pp. 109 - 112 |
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Main Authors | , , , , , , , , |
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Language | English |
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01.02.1998
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Abstract | Patients with chronic myeloproliferative disorders (CMD) show a high frequency of thrombosis. For this reason we evaluated endothelial cell markers, soluble adhesion molecule E‐selectin (sELAM), and thrombomodulin (TM) in 25 patients with CMD. Among them nine presented thromboses in their past history. Data were compared with those obtained in a group of healthy subjects and a group of patients with secondary thrombocytosis.
The mean plasma concentrations of sELAM were elevated in patients with CMD, as compared with healthy subjects (81.27 ± 42.8 ng/ml vs. 41.75 ± 13; P < 0.02). Similarly, the mean plasma concentrations of sTM were increased in CMD patients in comparison with the control group (102.0 ± 73 ng/ml vs. 16.7 ± 9.6; P < 0.01). More markedly elevated sELAM levels were observed in CMD patients with thrombosis than in patients without thrombosis (113.16 ± 29.5 ng/ml vs. 55.11 ± 19.1 ng/ml; P < 0.001), while no significant difference was found between CMD patients without thrombosis and secondary thrombocytosis (50.72 ± 10.8 ng/ml). Plasma thrombomodulin values in CMD patients with thrombosis (131 ± 93.8 ng/ml) were higher than those without thrombosis (65.77 ± 43.9 ng/ml; P < 0.02). sTM values were also significantly increased in patients with secondary thrombocytosis (P < 0.01).
It is speculated that the plasma, sELAM levels may reflect endothelium activation and that it is possibly useful in predicting the thrombotic risk in myeloproliferative disorders. Am. J. Hematol. 57:109–112, 1998. © 1998 Wiley‐Liss, Inc. |
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AbstractList | Patients with chronic myeloproliferative disorders (CMD) show a high frequency of thrombosis. For this reason we evaluated endothelial cell markers, soluble adhesion molecule E‐selectin (sELAM), and thrombomodulin (TM) in 25 patients with CMD. Among them nine presented thromboses in their past history. Data were compared with those obtained in a group of healthy subjects and a group of patients with secondary thrombocytosis.
The mean plasma concentrations of sELAM were elevated in patients with CMD, as compared with healthy subjects (81.27 ± 42.8 ng/ml vs. 41.75 ± 13; P < 0.02). Similarly, the mean plasma concentrations of sTM were increased in CMD patients in comparison with the control group (102.0 ± 73 ng/ml vs. 16.7 ± 9.6; P < 0.01). More markedly elevated sELAM levels were observed in CMD patients with thrombosis than in patients without thrombosis (113.16 ± 29.5 ng/ml vs. 55.11 ± 19.1 ng/ml; P < 0.001), while no significant difference was found between CMD patients without thrombosis and secondary thrombocytosis (50.72 ± 10.8 ng/ml). Plasma thrombomodulin values in CMD patients with thrombosis (131 ± 93.8 ng/ml) were higher than those without thrombosis (65.77 ± 43.9 ng/ml; P < 0.02). sTM values were also significantly increased in patients with secondary thrombocytosis (P < 0.01).
It is speculated that the plasma, sELAM levels may reflect endothelium activation and that it is possibly useful in predicting the thrombotic risk in myeloproliferative disorders. Am. J. Hematol. 57:109–112, 1998. © 1998 Wiley‐Liss, Inc. Patients with chronic myeloproliferative disorders (CMD) show a high frequency of thrombosis. For this reason we evaluated endothelial cell markers, soluble adhesion molecule E-selectin (sELAM), and thrombomodulin (TM) in 25 patients with CMD. Among them nine presented thromboses in their past history. Data were compared with those obtained in a group of healthy subjects and a group of patients with secondary thrombocytosis. The mean plasma concentrations of sELAM were elevated in patients with CMD, as compared with healthy subjects (81.27 +/- 42.8 ng/ml vs. 41.75 +/- 13; P < 0.02). Similarly, the mean plasma concentrations of sTM were increased in CMD patients in comparison with the control group (102.0 +/- 73 ng/ml vs. 16.7 +/- 9.6; P < 0.01). More markedly elevated sELAM levels were observed in CMD patients with thrombosis than in patients without thrombosis (113.16 +/- 29.5 ng/ml vs. 55.11 +/- 19.1 ng/ml; P < 0.001), while no significant difference was found between CMD patients without thrombosis and secondary thrombocytosis (50.72 +/- 10.8 ng/ml). Plasma thrombomodulin values in CMD patients with thrombosis (131 +/- 93.8 ng/ml) were higher than those without thrombosis (65.77 +/- 43.9 ng/ml; P < 0.02). sTM values were also significantly increased in patients with secondary thrombocytosis (P < 0.01). It is speculated that the plasma, sELAM levels may reflect endothelium activation and that it is possibly useful in predicting the thrombotic risk in myeloproliferative disorders. Patients with chronic myeloproliferative disorders (CMD) show a high frequency of thrombosis. For this reason we evaluated endothelial cell markers, soluble adhesion molecule E-selectin (sELAM), and thrombomodulin (TM) in 25 patients with CMD. Among them nine presented thromboses in their past history. Data were compared with those obtained in a group of healthy subjects and a group of patients with secondary thrombocytosis. The mean plasma concentrations of sELAM were elevated in patients with CMD, as compared with healthy subjects (81.27 +/- 42.8 ng/ml vs. 41.75 +/- 13; P < 0.02). Similarly, the mean plasma concentrations of sTM were increased in CMD patients in comparison with the control group (102.0 +/- 73 ng/ml vs. 16.7 +/- 9.6; P < 0.01). More markedly elevated sELAM levels were observed in CMD patients with thrombosis than in patients without thrombosis (113.16 +/- 29.5 ng/ml vs. 55.11 +/- 19.1 ng/ml; P < 0.001), while no significant difference was found between CMD patients without thrombosis and secondary thrombocytosis (50.72 +/- 10.8 ng/ml). Plasma thrombomodulin values in CMD patients with thrombosis (131 +/- 93.8 ng/ml) were higher than those without thrombosis (65.77 +/- 43.9 ng/ml; P < 0.02). sTM values were also significantly increased in patients with secondary thrombocytosis (P < 0.01). It is speculated that the plasma, sELAM levels may reflect endothelium activation and that it is possibly useful in predicting the thrombotic risk in myeloproliferative disorders. |
Author | Allegra, Alessandro Bellomo, Giacomo Tringali, Orazio Quartarone, Cristina Alonci, Andrea Musolino, Caterina Quartarone, Melchiorre Squadrito, Giovanni Spatari, Giovanna |
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Keywords | Human E Selectin Cell adhesion molecule Cardiovascular disease Malignant hemopathy Hemopathy Soluble form Thrombosis Blood plasma Vascular disease Myeloproliferative syndrome Chronic Complication Thromboembolism Thrombomodulin |
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References | 1987; 47 1984; 64 1990; 323 1995; 90 1993; 44 1986; 15 1994; 12 1993; 150 1992; 39 1985; 101 1992; 667 1996; 58 1985; 20 1992; 41 1988; 104 Newman W (e_1_2_1_11_2) 1993; 150 Nawroth PP (e_1_2_1_7_2) 1986; 15 Suzuki K (e_1_2_1_16_2) 1988; 104 e_1_2_1_6_2 e_1_2_1_4_2 e_1_2_1_5_2 e_1_2_1_3_2 e_1_2_1_12_2 Schaefer A (e_1_2_1_2_2) 1984; 64 e_1_2_1_10_2 e_1_2_1_15_2 e_1_2_1_13_2 e_1_2_1_14_2 e_1_2_1_8_2 e_1_2_1_17_2 e_1_2_1_9_2 |
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SubjectTerms | Adult Biological and medical sciences Biomarkers Chronic Disease E-Selectin - blood endothelial damage Female Hematologic and hematopoietic diseases Humans Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis Male Medical sciences Middle Aged myeloproliferative disorders Myeloproliferative Disorders - blood Myeloproliferative Disorders - complications soluble E‐selectin soluble thrombomodulin Thromboembolism - blood Thromboembolism - etiology Thrombomodulin - blood |
Title | Increased levels of the soluble adhesion molecule E‐selectin in patients with chronic myeloproliferative disorders and thromboembolic complications |
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