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临床试验/NCT01208792
NCT01208792已完成不适用

Auto-immunity and Prognosis of Pulmonary Arterial Hypertension

Assistance Publique - Hôpitaux de Paris6 个研究点 分布在 1 个国家目标入组 629 人开始时间: 2010年6月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
629
试验地点
6
主要终点
Immunological markers of prognosis interest in pulmonary arterial hypertension (PAH)

研究概览

简要总结

The investigators have recently evidenced the presence of antibodies to endothelial cells and fibroblasts in patients with idiopathic or SSc-associated PAH. The investigators also have identified several target antigens of anti-fibroblasts antibodies.

The objective of this study is to further investigate for the presence of antibodies to endothelial cells and fibroblasts in patients and characterize the antigen specificity of autoantibodies in patients with different types of non idiopathic and non SSc-associated PAH, such as PAH associated with HIV infection, porto-pulmonary hypertension, congenital heart diseases, systemic lupus erythematosus, mixed connective tissue disease and Sjögren's syndrome

详细描述

Two hundred and fifty patients with PAH will be included: 65 patients with idiopathic PAH (iPAH), 20 with PAH associated with HIV infection, 20 with porto-pulmonary hypertension, 20 with PAH secondary to congenital heart disorders, 40 with SSc, 20 with SLE, 20 with MCTD and 10 with a PAH associated with a Sjögren's syndrome.

Two hundred patients without PAH will also be included: 80 patients with SSc and 20 in each of the following groups: HIV infection, porto-pulmonary hypertension, SLE, congenital heart disorders, MCTD and with Sjögren's syndrome.

Twenty patients with proximal chronic thromboembolic pulmonary hypertension (CTPH) will also be included in a control arm of the study.

Two hundred and fifty healthy blood donors age and sex-matched with patients with PAH, will be included as controls.

By using 2D-immunoblotting techniques, we will evidence IgG antibodies to fibroblasts, EC, vascular smooth muscle cells (SMC) in multiple groups of patients and we will characterize target antigens of these autoantibodies. We will also assess the production of ROS: nitric oxide (NO), hydrogen peroxide (H2O2) and the effect of the whole serum (and the IgG particularly) on in VITRO proliferation of EC, fibroblasts and vascular SMC. For sera that will induce the production of ROS, we will study the effect of different vasodilatator (prostacycline, endothelin receptor antagonist, type 5 phosphodiesterase inhibitors) and anti-oxidant therapies.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Factorial
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • age over 18
  • for PAH patients: pre-capillary PAH evidenced by right-heart catheterization
  • no associated systemic disease for idiopathic PAH patients
  • for HIV patients, HIV1 infection confirmed by ELISA and western blot
  • for patients with porto pulmonary hypertension: evidence by endoscopy of esophageal varices, confirmation of hepatic venous pressure gradient over 5 mmHg by catheterization of the hepatic veins
  • for patients with congenital heart defect: evidence by imaging of atrial or ventricular septal defect, or patent ductus arterious and confirmed by heart catheterization
  • patients with SSc will fulfill the American College of Rheumatology (ACR) and the LEROY and MEDSGER criteria
  • patients with MCTD will fulfill the criteria for MCTD
  • patients with SLE will fulfill the updated and revised ACR criteria
  • patients with Sjögren's syndrome will fulfill the American-European consensus group criteria
  • patients with chronic thromboembolic pulmonary hypertension: Lung scintiscan showing segmental mismatched perfusion defects and confirmation by angiography of the occlusion and the chance of success of endarterectomy according to the location of disease
  • Signed written informed consent
  • Patients with health insurance

排除标准

  • age under 18
  • pregnant women
  • absence of written informed consent
  • associated malignant tumor

研究组 & 干预措施

Disease group

Experimental

Two hundred patients with PAH will be included: 50 patients with idiopathic PAH (iPAH), 20 with PAH associated with HIV infection, 20 with porto-pulmonary hypertension, 20 with PAH secondary to congenital heart disorders, 40 with SSc, 20 with SLE, 20 with MCTD and 10 with a PAH associated with a Sjögren's syndrome. Two hundred patients without PAH will also be included: 80 patients with SSc and 20 in each of the following groups: HIV infection, porto-pulmonary hypertension, SLE, congenital heart disorders, MCTD and with Sjögren's syndrome.

干预措施: skin biopsy (Procedure)

Disease group

Experimental

Two hundred patients with PAH will be included: 50 patients with idiopathic PAH (iPAH), 20 with PAH associated with HIV infection, 20 with porto-pulmonary hypertension, 20 with PAH secondary to congenital heart disorders, 40 with SSc, 20 with SLE, 20 with MCTD and 10 with a PAH associated with a Sjögren's syndrome. Two hundred patients without PAH will also be included: 80 patients with SSc and 20 in each of the following groups: HIV infection, porto-pulmonary hypertension, SLE, congenital heart disorders, MCTD and with Sjögren's syndrome.

干预措施: Blood Sample (Other)

Control group 1

Other

Two hundred healthy blood donors age and sex-matched with patients with PAH, will be included as controls.

干预措施: Blood Sample (Other)

Control group 2

Other

Twenty patients with proximal chronic thromboembolic pulmonary hypertension (CTPH) will also be included in a control arm of the study.

干预措施: Blood Sample (Other)

结局指标

主要结局

Immunological markers of prognosis interest in pulmonary arterial hypertension (PAH)

时间窗: one year

次要结局

  • Target antigens of autoantibodies(one year)
  • Subpopulations of patients with PAH whose serum is able to induce the production of reactive oxygen species (ROS)(one year)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (6)

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