Karakurt Cemşit, Başpınar Osman, Çelik Fazlı Serkan, Taşkapan Çağatay, Şahin Aydın Derya, Yoloğlu Saim
Department of Pediatric Cardiology, İnönü University Faculty of Medicine, Malatya, Turkey.
Department of Pediatric Cardiology, Gaziantep University Faculty of Medicine, Gaziantep, Turkey.
Balkan Med J. 2014 Sep;31(3):219-23. doi: 10.5152/balkanmedj.2014.13307. Epub 2014 Sep 1.
Pulmonary arterial hypertension secondary to untreated left-to-right shunt defects leads to increased pulmonary blood flow, endothelial dysfunction, increased pulmonary vascular resistance, vascular remodelling, neointimal and plexiform lesions. Some recent studies have shown that inflammation has an important role in the pathophysiology of pulmonary arterial hypertension.
The aim of this study is to evaluate serum pentraxin 3 and high sensitive (hs)-C reactive protein (hs-CRP) levels in children with severe pulmonary arterial hypertension (PAH) secondary to untreated congenital heart defects and evaluate the role of inflammation in pulmonary hypertension.
Cross sectional study.
After ethics committee approval and receiving consent from parents, there were 31 children were selected for the study with severe PAH, mostly with a left-to-right shunt, who had been assessed by cardiac catheterisation and were taking specific pulmonary vasodilators. The control group consisted of 39 age and gender matched healthy children. After recording data about all the patients including age, gender, weight, haemodynamic studies and vasodilator testing, a physical examination was done for all subjects. Blood was taken from patients and the control group using peripheral veins to analyse serum Pentraxin 3, N-terminal pro-Brain Natriuretic Peptide (NT-ProBNP) and hs-CRP levels. Serum Pentraxin-3 levels were measured by enzyme linked immunosorbent assay (ELISA) and expressed as ng/mL. Serum hs-CRP levels were measured with an immunonephelometric method and expressed as mg/dL. The serum concentration of NT-proBNP was determined by a chemiluminescent immunumetric assay and expressed as pg/mL.
Serum Pentraxin- 3 levels were determined to be 1.28±2.12 (0.12-11.43) in the PAH group (group 1) and 0.40±0.72 (0.07-3.45) in group 2. There was a statistically significant difference between the two groups (p<0.01). Serum hs-CRP levels were measured as 2.92±2.12 (0.32-14.7) mg/dL in group 1 and 0.35±0.16 (0.07-3.45) mg/dL in group 2. The hs-CRP level was increased in the PAH group to a significant degree (p<0.01).
Our study showed that pentraxin 3 and hs-CRP levels were increased significantly in the PAH group. We consider that inflammation plays an important role in severe pulmonary hypertension and progressive pulmonary arterial hypertension in children with PAH.
未经治疗的左向右分流性缺损继发的肺动脉高压会导致肺血流量增加、内皮功能障碍、肺血管阻力增加、血管重塑、新生内膜和丛状病变。最近的一些研究表明,炎症在肺动脉高压的病理生理学中起重要作用。
本研究旨在评估未经治疗的先天性心脏病继发的重度肺动脉高压(PAH)患儿的血清五聚素3和高敏(hs)-C反应蛋白(hs-CRP)水平,并评估炎症在肺动脉高压中的作用。
横断面研究。
经伦理委员会批准并获得家长同意后,选择31例重度PAH患儿进行研究,这些患儿大多有左向右分流,已通过心导管检查评估并正在服用特定的肺血管扩张剂。对照组由39名年龄和性别匹配的健康儿童组成。记录所有患者的年龄、性别、体重、血流动力学研究和血管扩张剂测试等数据后,对所有受试者进行体格检查。从患者和对照组的外周静脉采血,分析血清五聚素3、N末端脑钠肽前体(NT-ProBNP)和hs-CRP水平。血清五聚素-3水平通过酶联免疫吸附测定(ELISA)测量,以ng/mL表示。血清hs-CRP水平采用免疫比浊法测量,以mg/dL表示。NT-proBNP的血清浓度通过化学发光免疫分析法测定,以pg/mL表示。
PAH组(第1组)血清五聚素-3水平测定为1.28±2.12(0.12 - 11.43),第2组为0.40±0.72(0.07 - 3.45)。两组之间存在统计学显著差异(p<0.01)。第1组血清hs-CRP水平测量为2.92±2.12(0.32 - 14.7)mg/dL,第2组为0.35±0.16(0.07 - 3.45)mg/dL。PAH组的hs-CRP水平显著升高(p<0.01)。
我们的研究表明,PAH组中五聚素3和hs-CRP水平显著升高。我们认为炎症在PAH患儿的重度肺动脉高压和进行性肺动脉高压中起重要作用。