Borowiec Anna, Hadzik-Błaszczyk Małgorzata, Kowalik Ilona, Rusinowicz Tomasz, Krupa Renata, Jankowski Jan, Kandyba Piotr, Józefik Ewa, Gawałkiewicz Anna, Życińska Katarzyna
Medical University of Warsaw, Poland.
Sarcoidosis Vasc Diffuse Lung Dis. 2019;36(3):202-208. doi: 10.36141/svdld.v36i3.8088. Epub 2019 May 1.
Granulomatosis with polyangiitis (GPA), previously known as Wegener's granulomatosis, is one of antineutrophil cytoplasmic autoantibody (ANCA) - associated vasculitis. In patients with GPA an increased incidence of venous thromboembolism (VTE), mainly during active disease, has been described. The aim of the present study was to assess the incidence of VTE and its relation with classic risk factors for atherosclerosis, presence of coronary artery disease (CAD), echocardiographic parameters and laboratory findings in GPA patients.
The group of consecutive patients with GPA were followed in the study. In all patients echocardiography and laboratory tests were performed.
Ninety six patients with GPA were followed for mean 3 years. In 16 patients (16.6%) VTEs occurred in association with GPA, of which 56% occurred 6 months before or one year after diagnosis of GPA. Classic risk factors for atherosclerosis were present in 77 patients (80.2%) at some moment during follow-up. In patients with VTE there were larger right ventricle diameter (p=0.041) and higher right ventricle systolic pressure (p=0.022) observed. VTEs occurred significantly less frequently in patients treated with cyclophosphamide (p=0.049). In this study group VTE occurred more frequently than CAD: 16 (16.7%) vs. 4 (4.2%); p=0,0049. Patients with VTE were younger than those with CAD (p=0.053) and had higher levels of ANCA-PR 3 (p=0.016).
Patients with granulomatosis with polyangiitis in first years after diagnosis have higher risk of venous thromboembolism than coronary artery disease. This finding is probably related to hypercoagulability induced by the disease and its therapy.
肉芽肿性多血管炎(GPA),既往称为韦格纳肉芽肿,是抗中性粒细胞胞浆抗体(ANCA)相关性血管炎之一。据描述,GPA患者静脉血栓栓塞(VTE)发生率增加,主要发生在疾病活动期。本研究的目的是评估GPA患者VTE的发生率及其与动脉粥样硬化经典危险因素、冠状动脉疾病(CAD)的存在、超声心动图参数和实验室检查结果的关系。
本研究对连续的GPA患者进行随访。所有患者均进行了超声心动图和实验室检查。
96例GPA患者平均随访3年。16例(16.6%)患者发生VTE与GPA相关,其中56%发生在GPA诊断前6个月或诊断后1年。在随访的某个时刻,77例(80.2%)患者存在动脉粥样硬化的经典危险因素。VTE患者的右心室直径较大(p=0.041),右心室收缩压较高(p=0.022)。接受环磷酰胺治疗的患者VTE发生率显著较低(p=0.049)。在该研究组中,VTE的发生率高于CAD:16例(16.7%)对4例(4.2%);p=0.0049。VTE患者比CAD患者年轻(p=0.053),且ANCA-PR 3水平较高(p=0.016)。
肉芽肿性多血管炎患者在诊断后的头几年发生静脉血栓栓塞的风险高于冠状动脉疾病。这一发现可能与疾病及其治疗引起的高凝状态有关。