Najean Y, Poirier O
Acta Haematol. 1984;72(2):83-9. doi: 10.1159/000206365.
34 polycythemic patients, in complete or partial stable remission, were studied for beta-thromboglobulin (beta-TG) and platelet factor 4 (PF-4) before, during and after treatment by an antiaggregating agent, ticlopidine, in comparison with 30 untreated patients. The cases with initial high value have an obvious drop, which is still maintained at the 2nd month after treatment, independent of variations of red cell and platelet counts. Any long-term protocol for clinical evaluation of antiaggregating therapy in myelo-proliferative diseases should be founded on evaluation of the markers of platelet function.
对34例完全或部分处于稳定缓解期的红细胞增多症患者在使用抗血小板聚集剂噻氯匹定治疗前、治疗期间及治疗后进行了β-血小板球蛋白(β-TG)和血小板第4因子(PF-4)的研究,并与30例未治疗的患者进行了比较。初始值较高的病例有明显下降,治疗后第2个月仍维持下降,与红细胞和血小板计数的变化无关。任何关于骨髓增殖性疾病抗血小板聚集治疗临床评估的长期方案都应基于血小板功能标志物的评估。