Department of Cardiology, Medical University of Bialystok, ul. M. Sklodowskiej-Curie 24 A, 15-276 Bialystok, Poland.
Department of Allergology and Internal Medicine, Medical University of Bialystok, ul. M. Sklodowskiej-Curie 24 A, 15-276 Bialystok, Poland.
Cytokine. 2014 Mar;66(1):40-5. doi: 10.1016/j.cyto.2013.12.013. Epub 2014 Jan 14.
Inflammation may play a pivotal role in the pathogenesis of pulmonary arterial hypertension (PAH). We evaluated the concentrations of serum sTWEAK, its scavenger receptor sCD163 and sTWEAK/sCD163 ratio in patients with PAH.
The study enrolled 26 stable patients with PAH confirmed by right heart catheterization and 24 healthy volunteers matched for age, sex and body weight. All patients underwent transthoracic echocardiography, cardiopulmonary exercise test, 6-min walk test, measurement of lung diffusing capacity for the carbon monoxide (DLCO) and venous blood tests. Concentrations of sTWEAK and sCD163 were determined using ELISA kits.
The PAH patients were characterized by significantly higher median serum sCD163 levels (1072 vs 890ng/ml, p=0.04) together with lower serum sTWEAK concentrations (200 vs 278.1pg/ml, p=0.003) comparing to control subjects. sTWEAK/sCD163 ratio was therefore significantly lower in PAH group (0.18 vs 0.33, p=0.0005). No correlation was found between sTWEAK and sCD163 concentrations in both groups. We observed statistically significant inverse correlation between peak VO2 consumption and sCD163 concentrations (r=-0.52, p<0.05) and positive with sTWEAK/sCD163 ratio (r=0.45, p<0.05) in PAH group. Moreover, sTWEAK/sCD163 ratio positively correlated with % of predicted values of DLCO (r=0.42, p<0.05).
Patients with PAH present altered serum sTWEAK and sCD163 levels. The sTWEAK/sCD163 ratio appears to be a better indicator of the severity of PAH as compared to sTWEAK or sCD163 alone. The exact role of sCD163 or interaction between CD163 and sTWEAK in the initiation or progression of PAH as well as their potential prognostic significance remains to be established.
炎症可能在肺动脉高压(PAH)的发病机制中起关键作用。我们评估了血清 sTWEAK、其清道夫受体 sCD163 和 sTWEAK/sCD163 比值在 PAH 患者中的浓度。
这项研究纳入了 26 例经右心导管检查确诊的稳定型 PAH 患者和 24 例年龄、性别和体重匹配的健康志愿者。所有患者均接受了经胸超声心动图、心肺运动试验、6 分钟步行试验、一氧化碳肺弥散量(DLCO)测定和静脉血检查。采用 ELISA 试剂盒测定 sTWEAK 和 sCD163 的浓度。
与对照组相比,PAH 患者的血清 sCD163 水平中位数明显更高(1072 与 890ng/ml,p=0.04),血清 sTWEAK 浓度明显更低(200 与 278.1pg/ml,p=0.003)。因此,PAH 组的 sTWEAK/sCD163 比值明显更低(0.18 与 0.33,p=0.0005)。两组中 sTWEAK 与 sCD163 浓度之间均无相关性。我们观察到 PAH 组中峰值 VO2 消耗与 sCD163 浓度之间呈统计学显著负相关(r=-0.52,p<0.05),与 sTWEAK/sCD163 比值之间呈统计学显著正相关(r=0.45,p<0.05)。此外,sTWEAK/sCD163 比值与预测值的 %DLCO 呈正相关(r=0.42,p<0.05)。
PAH 患者存在血清 sTWEAK 和 sCD163 水平改变。与 sTWEAK 或 sCD163 单独相比,sTWEAK/sCD163 比值似乎是 PAH 严重程度的更好指标。sCD163 或 CD163 与 sTWEAK 之间的相互作用在 PAH 的发生或进展中的确切作用及其潜在的预后意义仍有待确定。