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Macrophage migration inhibitory factor is an early marker of severe acute pancreatitis based on the revised Atlanta classification

机译:巨噬细胞迁移抑制因子是基于修订的亚特兰大分类的严重急性胰腺炎的早期标志物

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Various serum markers for early identification of severe acute pancreatitis (SAP) have been studied. Serum macrophage migration inhibitory factor (MIF) was reported to be correlated with severity of acute pancreatitis (AP) based on the 1992 Atlanta classification. However, MIF has never been proven to be predictive of disease severity based on the revised Atlanta classification (RAC). The potential predictive value of MIF needs to be further validated. Consecutive patients with AP within 48?h after symptom onset and 10 healthy control volunteers were enrolled prospectively. Serum MIF levels were measured by enzyme-linked immunosorbent assay (ELISA). The predictive value of MIF, clinical scores and other serum markers were determined. Among 143 patients with AP, there were 52 (36.4%), 65 (45.5%) and 26 (18.1%) with mild, moderate and severe disease based on the RAC respectively. Compared with healthy volunteers, serum levels of MIF were significantly higher in AP patients, especially those with SAP (P??0.001). Multivariate regression analysis indicated that increased serum MIF (cut-off 2.30?ng/ml, OR?=?3.16, P?=?0.008), IL-6 (cut-off 46.8?pg/ml, OR?=?1.21, P?=?0.043), APACHE II score (cut-off 7.5, OR?=?2.57, P?=?0.011) and BISAP score (cut-off 1.5, OR?=?1.01, P?=?0.038) were independent risk factors for predicting SAP (P??0.05). By using the area under the receiver operating characteristic (ROC) curve (AUC), MIF (AUC 0.950) demonstrated more excellent discriminative power for predicting SAP than APACHE II (AUC 0.899), BISAP (AUC 0.886), and IL-6 (AUC 0.826). Serum MIF is a valuable early marker for predicting the severity of AP based on the RAC.
机译:研究了用于早期鉴定严重急性胰腺炎(SAP)的各种血清标志物。据报道,血清巨噬细胞迁移抑制因子(MIF)与1992年亚特兰大分类的急性胰腺炎(AP)的严重程度相关。然而,基于修订的亚特兰大分类(RAC),MIF从未被证明预测疾病严重程度。 MIF的潜在预测值需要进一步验证。在症状发作后48岁以下的AP患者,症状发作后,并令人医前注册了10名健康控制志愿者。通过酶联免疫吸附测定(ELISA)测量血清MIF水平。确定MIF,临床评分和其他血清标记物的预测值。在143例AP患者中,分别存在52例(36.4%),65(45.5%)和26(18.1%),分别基于RAC的温和,中度和严重的疾病。与健康志愿者相比,AP患者的MIF血清MIF显着较高,尤其是含有SAP的血清(P 1 0.001)显着更高。多变量回归分析表明,增加血清MIF(切断2.30≤ng/ ml,或?3.16,p?= 0.008),IL-6(切断46.8·pg / ml,或?=?1.21, p?=?0.043),Apache II得分(切断7.5,或?=?2.57,P?0.011)和BISAP得分(切断1.5,或?=?1.01,P?= 0.038)是用于预测SAP的独立风险因素(p?&?0.05)。通过使用接收器操作特性(ROC)曲线(AUC)的区域,MIF(AUC 0.950)显示了用于预测SAP的更优异的辨别力,而不是Apache II(AUC 0.899),BISAP(AUC 0.886)和IL-6(AUC 0.826)。血清MIF是一种有价值的早期标记,用于预测基于RAC的AP的严重程度。

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