促血管生成细胞因子在预测发热性中性粒细胞增多症癌症患儿败血症中的作用。

Selma Çakmakcı, Neriman Sarı, Çiğdem Sönmez, İnci Ergürhan İlhan
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引用次数: 0

摘要

背景:我们评估了脓毒症的发生与癌症相关发热性中性粒细胞减少症儿科患者血清中血管生成素(Ang-1、Ang-2)、血管内皮生长因子(VEGF)和可溶性fms样酪氨酸激酶-1(sFlt-1)水平之间的关系:研究人员对2016年6月至2018年6月期间发生86次发热性中性粒细胞减少症(FN)的52名恶性肿瘤患儿进行了研究。每次发热性中性粒细胞减少被视为一个独立事件,并记录了发热性中性粒细胞减少的总数(86次发热性中性粒细胞减少=发热性中性粒细胞减少组)。对照组由 21 名健康儿童组成。在每次FN发作的基线和第48小时测量Ang-1、Ang-2、VEGF-A和sFlt-1,同时对炎症进行常规定性(C反应蛋白、白细胞和绝对中性粒细胞计数):结果:在这些病例中,29 例(34.5%)发生了败血症,57 例被归类为非并发症 FN。患者和对照组的 Ang-1、Ang-2、血管内皮生长因子和 sFlt-1 的基线值有显著差异(均为 P <0.05)。在脓毒症亚组中,Ang-2 值高于无脓毒症亚组(P = 0.017)。在预测脓毒症方面,当截断值为 74.6 时,Ang-2 的灵敏度为 60.7%,特异度为 66.7%(AUC:0.662 [95%CI:0.541 - 0.783],p = 0.022);当截断值为 0.405 时,Ang-2/Ang-1 比率的灵敏度为 65.5%,特异度为 60.0%(AUC:0.633 [95%CI:0.513 - 0.753],p = 0.046):我们的研究结果表明,脓毒症组的Ang-2和Ang-2/Ang-1较高,Ang-2可能是提示FN和/或癌症患者脓毒症风险的生物标志物。
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The role of proangiogenic cytokines in predicting sepsis in febrile neutropenic children with cancer.

Background: We assessed the relationship between sepsis occurrence and the serum levels of angiopoietin (Ang-1, Ang-2), vascular endothelial growth factor (VEGF) and soluble fms-like tyrosine kinase-1 (sFlt-1) in pediatric patients with cancer-related febrile neutropenia.

Methods: Fifty-two children with malignant tumors who experienced 86 episodes of febrile neutropenia (FN) were examined between June 2016 and June 2018. Each FN episode was considered a separate event and the total number of FNs were recorded (86 FN episodes = FN group). The control group consisted of 21 healthy children. Ang-1, Ang-2, VEGF-A and sFlt-1 were measured at the baseline and 48th hour of each FN episode -alongside routine characterization of inflammation (C-reactive protein; white blood cell and absolute neutrophil count).

Results: Among the episodes, 29 (34.5%) developed sepsis while 57 were classified as non-complicated FN. The baseline values of patients and controls were significantly different for Ang-1, Ang-2, VEGF and sFlt-1 values (all, p < 0.05). In the subgroup with sepsis, Ang-2 values were higher than in the subgroup without sepsis (p = 0.017). In predicting sepsis, Ang-2 had 60.7% sensitivity and 66.7% specificity at the 74.6 cut-off value (AUC: 0.662 [95%CI: 0.541 - 0.783], p = 0.022), Ang-2 / Ang-1 ratio had 65.5% sensitivity and 60.0% specificity at the 0.405 cut-off value (AUC: 0.633 [95%CI: 0.513 - 0.753], p = 0.046).

Conclusions: Our results reveal that Ang-2 and Ang-2/Ang-1 were higher in the sepsis group and Ang-2 might be a biomarker to indicate the risk of sepsis in patients with FN and/or cancer.

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