Peripheral Blood Plasminogen Activator Inhibitor 1 and Tissue-Type Plasminogen Activator-Inhibitor Complex Levels for the Diagnosis and Prediction Value of Venous Thromboembolism in Malignant Tumors.

Na Yu, Minghao Shi, Honghong Li, Zhongjun Shen, Ying Sun, Yao Li, Xiaoyi Liu, Liyan Zhao
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Abstract

Context.—: Patients with malignant tumors complicated by venous thromboembolism (VTE) face high mortality rates because of a lack of effective diagnostic and predictive markers. Plasminogen activator inhibitor 1 (PAI-1) and tissue-type plasminogen activator-inhibitor complex (t-PAIC) may contribute to VTE formation in these patients.

Objective.—: To evaluate the diagnostic and predictive value of peripheral blood PAI-1 and t-PAIC levels in patients with malignant tumors complicated by VTE and to develop a new thrombosis risk score model (NRS) based on PAI-1 levels.

Design.—: This study included 216 patients with malignant tumors (lung, colorectal, ovarian, breast, and gastric cancers). The correlation between PAI-1 and t-PAIC levels was explored. The predictive value of PAI-1 and t-PAIC, combined with the COMPASS-CAT risk score, Khorana risk score, and Padua risk score, was assessed for postoperative VTE risk. Differences in PAI-1 and t-PAIC levels across tumor types were also analyzed.

Results.—: The PAI-1 and t-PAIC levels were positively correlated. Preintervention PAI-1 levels independently predicted VTE risk, and the new thrombosis risk score model could effectively predict the occurrence of concurrent VTE in patients with malignancy. PAI-1 and t-PAIC have better diagnostic value for VTE than D-dimers. Combining these markers with the COMPASS-CAT risk score, Khorana risk score, and Padua risk score improves the risk prediction of VTE. PAI-1 levels were significantly associated with VTE risk in colorectal cancer, whereas t-PAIC levels were significantly associated with VTE risk in breast cancer.

Conclusions.—: Peripheral blood PAI-1 and t-PAIC levels have excellent predictive and diagnostic value for VTE in patients with malignancy.

外周血纤溶酶原激活物抑制剂1和组织型纤溶酶原激活物抑制剂复合物水平对恶性肿瘤静脉血栓栓塞的诊断和预测价值。
上下文。-:由于缺乏有效的诊断和预测指标,恶性肿瘤合并静脉血栓栓塞(VTE)患者面临着高死亡率。纤溶酶原激活物抑制剂1 (PAI-1)和组织型纤溶酶原激活物-抑制剂复合物(t-PAIC)可能有助于这些患者静脉血栓栓塞的形成。-:评价外周血PAI-1和t- pai水平对恶性肿瘤合并静脉血栓栓塞患者的诊断和预测价值,建立基于PAI-1水平的血栓形成风险评分新模型(NRS)。-:本研究纳入216例恶性肿瘤患者(肺癌、结直肠癌、卵巢癌、乳腺癌、胃癌)。探讨PAI-1与t- pai水平的相关性。结合COMPASS-CAT风险评分、Khorana风险评分和Padua风险评分,评估PAI-1和t- pac对术后静脉血栓栓塞风险的预测价值。还分析了不同肿瘤类型PAI-1和t- pai水平的差异。-: PAI-1与t- pai水平呈正相关。干预前PAI-1水平独立预测VTE风险,新的血栓形成风险评分模型可有效预测恶性肿瘤患者并发VTE的发生。PAI-1和t- pai对VTE的诊断价值优于d -二聚体。将这些指标与COMPASS-CAT风险评分、Khorana风险评分和Padua风险评分相结合,可提高VTE的风险预测。PAI-1水平与结直肠癌静脉血栓栓塞风险显著相关,而t- pai水平与乳腺癌静脉血栓栓塞风险显著相关。-:外周血PAI-1和t- pai水平对恶性静脉血栓栓塞患者有极好的预测和诊断价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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