Keranov Stanislav, Dörr Oliver, Jafari Leili, Liebetrau Christoph, Keller Till, Troidl Christian, Kriechbaum Steffen, Voss Sandra, Richter Manuel, Tello Khodr, Gall Henning, Ghofrani Hossein A, Mayer Eckhard, Seeger Werner, Hamm Christian W, Nef Holger
Department of Cardiology and Angiology, University of Giessen, Giessen, Germany.
DZHK (German Center for Cardiovascular Research), Partner Site RheinMain, Bad Nauheim, Germany.
Biomarkers. 2020 May;25(3):290-295. doi: 10.1080/1354750X.2020.1745889. Epub 2020 Apr 5.
This study assessed the utility of SPARC-like protein 1 (SPARCL1) as a biomarker of maladaptive right ventricular (RV) function in patients with pulmonary hypertension (PH). In this prospective study, we examined SPARCL1 levels in 105 patients with adaptive ( = 34) and maladaptive RV ( = 32) pressure overload caused by PH, dilated cardiomyopathy (DCM, = 18) with LVEF < 35% and preserved RV function and controls without LV or RV abnormalities ( = 21). The median SPARCL1 concentration in patients with maladaptive RV function was higher than in those with adaptive RV function ( < 0.01), DCM ( < 0.001) or controls ( < 0.001). Patients with adaptive RV function had higher SPARCL1 concentrations than controls ( < 0.05), whereas there was no difference between adaptive RV and DCM. SPARCL1 showed good predictive power for maladaptive RV (AUC 0.77, < 0.001) with an optimal cut-off value of 9.66 ng/ml. The TAPSE/PASP ratio was the only independent predictor of SPARCL1 ≥ 9.66 ng/ml in multivariable logistic regression analysis. SPARCL1 shows potential as novel biomarker of RV pathological remodelling and is associated with RV maladaptation and ventriculoarterial uncoupling in PH.
本研究评估了类 Sparc 样蛋白 1(SPARCL1)作为肺动脉高压(PH)患者右心室(RV)功能不良生物标志物的效用。在这项前瞻性研究中,我们检测了 105 例患者的 SPARCL1 水平,这些患者包括因 PH 导致适应性 RV 压力过载(n = 34)和非适应性 RV 压力过载(n = 32)、左心室射血分数(LVEF)< 35%且 RV 功能保留的扩张型心肌病(DCM,n = 18)以及无左心室或右心室异常的对照组(n = 21)。非适应性 RV 功能患者的 SPARCL1 浓度中位数高于适应性 RV 功能患者(P < < 0.01)、DCM 患者(P < < 0.001)或对照组(P < < 0.001)。适应性 RV 功能患者的 SPARCL1 浓度高于对照组(P < < 0.05),而适应性 RV 与 DCM 之间无差异。SPARCL1 对非适应性 RV 具有良好的预测能力(曲线下面积 0.77,P < < 0.001),最佳截断值为 9.66 ng/ml。在多变量逻辑回归分析中,TAPSE/PASP 比值是 SPARCL1≥9.66 ng/ml 的唯一独立预测因子。SPARCL1 显示出作为 RV 病理重塑新生物标志物的潜力,并且与 PH 患者的 RV 功能不良及心室动脉解偶联相关。