Kocaeli University, School of Medicine, Department of Hematology, Kocaeli, Turkey.
Kocaeli University, School of Medicine, Department of Internal Medicine, Kocaeli, Turkey.
Turk J Haematol. 2012 Jun;29(2):162-9. doi: 10.5505/tjh.2012.03780. Epub 2012 Jun 15.
Vascular events are a common complication in patients with polycythemia vera (PV) and essential thrombocythemia (ET). This study aimed to analyze the association between PAI-1 4G/5G and ACE I/D gene polymorphisms, and leukocytosis with thrombosis in patients with PV and ET.
In total, 64 patients with ET and PV were evaluated. Arterial or venous thrombosis, such as cerebral transient ischemic attack, ischemic stroke, myocardial infarction, peripheral arterial thrombosis, deep venous thrombosis, and pulmonary embolism, were defined as a vascular event. DNA samples were screened for mutations via reverse hybridization strip assay.
In terms of PAI-1 gene polymorphism, the frequency of the 4G and 5G allele was 48.5% and 51.5%, respectively. The ACE allele frequency was 51.2% and 48.8% for D and I, respectively. There wasn't an association between occurrence of vascular events and the frequency of any allele. In terms of occurrence of vascular events, there weren't any significance differences between the patients that were carrying the ACE D/D homozygous allele to ACE I/D and those that carried the I/I allele (P = 0.93). There wasn't a significant difference in occurrence of vascular events between the PAI-1 5G/5G homozygote allele carriers, and the 4G/5G and 4G/4G allele carriers (P = 0.97). Vascular events were significantly more common in the patients with leukocytosis (leukocyte count >10 × 109 L-1) than in those without leukocytosis (leukocyte count ≤10 × 109 L-1) (P = 0.00). Age >60 years was also a significant risk factor for occurrence of vascular events(P = 0.008).
PAI-1 and ACE gene polymorphisms were not considered new risk factors for thrombosis in PV and ET patients. On the other hand, leukocytosis at diagnosis was associated with the occurrence of vascular events in the patients with ET and PV.
血管事件是真性红细胞增多症(PV)和原发性血小板增多症(ET)患者的常见并发症。本研究旨在分析 PAI-1 4G/5G 和 ACE I/D 基因多态性以及白细胞增多与 PV 和 ET 患者血栓形成之间的关系。
共评估了 64 例 ET 和 PV 患者。动脉或静脉血栓形成,如短暂性脑缺血发作、缺血性中风、心肌梗死、外周动脉血栓形成、深静脉血栓形成和肺栓塞,被定义为血管事件。通过反向杂交条带分析筛选 DNA 样本中的突变。
PAI-1 基因多态性方面,4G 和 5G 等位基因的频率分别为 48.5%和 51.5%。ACE 等位基因频率分别为 D 和 I 的 51.2%和 48.8%。血管事件的发生与任何等位基因的频率之间没有关联。在发生血管事件方面,携带 ACE D/D 纯合等位基因的患者与携带 ACE I/D 和 I/I 等位基因的患者之间没有统计学差异(P = 0.93)。PAI-1 5G/5G 纯合子等位基因携带者与 4G/5G 和 4G/4G 等位基因携带者之间发生血管事件的差异无统计学意义(P = 0.97)。白细胞增多(白细胞计数>10×109 L-1)的患者比白细胞计数正常(白细胞计数≤10×109 L-1)的患者更易发生血管事件(P = 0.00)。年龄>60 岁也是发生血管事件的显著危险因素(P = 0.008)。
PAI-1 和 ACE 基因多态性不能作为 PV 和 ET 患者血栓形成的新危险因素。另一方面,在 ET 和 PV 患者中,诊断时的白细胞增多与血管事件的发生有关。