Department of Hepatobiliary and Pancreatosplenic Surgery, Zhuzhou Central Hospital, Zhuzhou, 412007, Hunan Province, China.
Department of Pancreatic Surgery, General Surgery, Xiangya Hospital, Central South University, 87 Xiangya Rd, Changsha, 410008, Hunan Province, China.
BMC Gastroenterol. 2021 Jan 22;21(1):34. doi: 10.1186/s12876-020-01598-0.
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.
已经研究了各种用于早期识别重症急性胰腺炎(SAP)的血清标志物。根据 1992 年亚特兰大分类,血清巨噬细胞移动抑制因子(MIF)与急性胰腺炎(AP)的严重程度相关。然而,根据修订后的亚特兰大分类(RAC),MIF 从未被证明可预测疾病的严重程度。MIF 的潜在预测价值需要进一步验证。
前瞻性连续纳入发病 48 小时内的急性胰腺炎患者和 10 名健康对照志愿者。通过酶联免疫吸附试验(ELISA)测定血清 MIF 水平。确定 MIF、临床评分和其他血清标志物的预测价值。
在 143 例 AP 患者中,根据 RAC,分别有 52 例(36.4%)、65 例(45.5%)和 26 例(18.1%)为轻症、中症和重症。与健康志愿者相比,AP 患者血清 MIF 水平明显升高,尤其是 SAP 患者(P<0.001)。多变量回归分析表明,血清 MIF 升高(截断值 2.30ng/ml,OR=3.16,P=0.008)、IL-6(截断值 46.8pg/ml,OR=1.21,P=0.043)、APACHE II 评分(截断值 7.5,OR=2.57,P=0.011)和 BISAP 评分(截断值 1.5,OR=1.01,P=0.038)是预测 SAP 的独立危险因素(P<0.05)。通过受试者工作特征(ROC)曲线下面积(AUC),MIF(AUC 0.950)预测 SAP 的鉴别能力优于 APACHE II(AUC 0.899)、BISAP(AUC 0.886)和 IL-6(AUC 0.826)。
血清 MIF 是预测 RAC 下 AP 严重程度的有价值的早期标志物。