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血清肿瘤坏死因子相关凋亡诱导配体水平与肺动脉高压的严重程度相关。

Serum levels of tumor necrosis factor-related apoptosis-inducing ligand correlate with the severity of pulmonary hypertension.

作者信息

Liu Huan, Yang Erli, Lu Xiaolan, Zuo Caojian, He Yuhu, Jia Daile, Zhu Qian, Yu Ying, Lv Ankang

机构信息

Department of Cardiology, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200025, China; Key Laboratory of Food Safety Research, Institute for Nutritional Sciences, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China.

Department of Cardiology, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200025, China.

出版信息

Pulm Pharmacol Ther. 2015 Aug;33:39-46. doi: 10.1016/j.pupt.2015.06.002. Epub 2015 Jun 15.

DOI:10.1016/j.pupt.2015.06.002
PMID:26086178
Abstract

Pulmonary hypertension (PH) is a rapidly progressive disease that eventually leads to right heart failure and death. Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) and its receptors (TRAIL-Rs) play an important role in the survival, migration, and proliferation of vascular smooth muscle cells. However, the association between serum TRAIL levels and PH is unknown. In this study, we assayed the serum soluble TRAIL (sTRAIL) levels in 78 patients with PH and 80 controls. The sTRAIL concentrations were elevated in the PH patients compared with the controls (138.76 ± 6.60 pg/mL vs. 80.14 ± 3.38 pg/mL, p < 0.0001). The presence of sTRAIL levels of >103 pg/mL could discriminate PH patients from healthy individuals, with a sensitivity of 75.6% and specificity of 81.2%. Moreover, elevated sTRAIL concentrations were associated with eventual pathological complications; this is consistent with the finding that sTRAIL levels decreased in patients who responded to treatment. In a hypoxia-induced PH mouse model, sTRAIL levels were significantly higher compared with those in normoxia mice, and clearly decreased when the mice were treated with treprostinil. The sTRAIL levels were positively correlated with right ventricular systolic pressure and the index of right ventricular hypertrophy. In conclusion, serum sTRAIL could be a biomarker for diagnosis and effective therapy for PH patients.

摘要

肺动脉高压(PH)是一种迅速进展的疾病,最终会导致右心衰竭和死亡。肿瘤坏死因子相关凋亡诱导配体(TRAIL)及其受体(TRAIL-Rs)在血管平滑肌细胞的存活、迁移和增殖中起重要作用。然而,血清TRAIL水平与PH之间的关联尚不清楚。在本研究中,我们检测了78例PH患者和80例对照者的血清可溶性TRAIL(sTRAIL)水平。与对照组相比,PH患者的sTRAIL浓度升高(138.76±6.60 pg/mL对80.14±3.38 pg/mL,p<0.0001)。sTRAIL水平>103 pg/mL可将PH患者与健康个体区分开来,敏感性为75.6%,特异性为81.2%。此外,sTRAIL浓度升高与最终的病理并发症相关;这与对治疗有反应的患者sTRAIL水平降低的发现一致。在缺氧诱导的PH小鼠模型中,与常氧小鼠相比,sTRAIL水平显著更高,并且在用曲前列尼尔治疗小鼠时明显降低。sTRAIL水平与右心室收缩压和右心室肥厚指数呈正相关。总之,血清sTRAIL可能是PH患者诊断和有效治疗的生物标志物。

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