1 / 1

Thrombin generation in two families with MYH-9-related platelet disorder

Thrombin generation in two families with MYH-9-related platelet disorder. Eva Zetterberg, MD, PhD 1 , Margareta S Carlsson Alle , MD, PhD 2, Jari Nivala , MD 3 , Juliane Najm , PhD 4 , Andreas Greinacher , MD 5

bao
Download Presentation

Thrombin generation in two families with MYH-9-related platelet disorder

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Thrombin generation in two families with MYH-9-related platelet disorder Eva Zetterberg, MD, PhD1, Margareta S CarlssonAlle, MD, PhD2, JariNivala, MD3, JulianeNajm, PhD4, Andreas Greinacher, MD5 1Department of Hematology and Coagulation, Skane University hospital, Malmö, Sweden; 2Department of Hematology, Växjö Central hospital, Växjö, Sweden; 3Department of Pediatrics, Karlstad, Sweden; 4Institute for Human Genetics, Greifswald, Germany; 4 Institute of Immunology and Transfusion Medicine, Greifswald, Germany Corresponding author: Eva Zetterberg, Department of Hematology and Coagulation, Jan Waldenströmsgata 14, plan 3b, 205 02, Malmö, Sweden. Phone: +46 40337436; Fax:+46 40336255; e-mail: eva.zetterberg@med.lu.se Results Plasma samples from 6 members from 2 families (A and B) were analyzed (fig 2). All patients were diagnosed MYH-9 related disease based on the presence of macrothrombocytopeniaand inclusion bodies in leucocytes. Two individuals in family A presented with arterial thrombosis before 50 years of age (marked with a star in Fig 3). Thrombin generation analysis revealed that these two members had an ETP within in the normal range despite a low platelet count (Table 1). Members of family B had ETP values below the normal range as expected by the low platelet count . When platelets from a healthy control was added to platelet poor plasma from patients A:1 and A:2 the ETP did not increase significantly. Figure 2 Figure 3 Introduction MYH-9 related platelet disorders are inherited macrothrombocytopenias where additional clinical manifestations including renal failure, hearing loss, pre senile cataract and inclusion bodies in leucocytes are present in different combinations. The bleeding tendency is usually mild to moderate but rarely, thrombotic complications are also seen . We report on the thrombin generation potential (ETP) in MYH9 patients with and without arterial thrombosis. • Normal range Methods Thrombin generation was performed on frozen platelet rich plasma using the calibrated automated thrombogram (CAT) method(Fig 1). ETP was compared between patients diagnosed with MYH-9 related platelet disorder and a reference material consisting of 40 healthy individuals. Table 1 • Conclusions • Patients MYH-9-related platelet disorder can have a normal ETP despite a low platelet counts • We suggest that plasma factors compensated for the low platelet count and clinically even led to a breakthrough of arterial thrombosis • We suggest that other centers also assess the ETP in their MYH-9 patients according tour protocol (www.med.lu.se/klinvetmalmo/koagulationsforskning/forskningsprojekt) to gather data on the potential association of the ETP with the phenotype.

More Related