Ginzburg Gila, Debnath Pradipta, Zhang Yin, Ata Nadeen Abu, Farrell Peter R, Garlapally Vineet, Kotha Nicole, Thompson Tyler, Vitale David S, Trout Andrew T, Abu-El-Haija Maisam
Department of Gastroenterology, Children's Wisconsin, Milwaukee, WI, USA.
Department of Radiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Dig Liver Dis. 2025 Feb;57(2):519-525. doi: 10.1016/j.dld.2024.10.009. Epub 2024 Oct 28.
Acute pancreatitis (AP) increases the risk of diabetes mellitus (DM). Our aim was to identify clinical, laboratory and imaging predictors of preDM/DM in youth post index AP.
This was a prospective cohort study of patients ≤21 years-old with an index admission for AP and follow up at 3 and/or 12 months. Clinical laboratory values, imaging findings, admission course, and plasma chemokine and cytokine measures collected at index admission were tested for association with preDM/DM development. A multivariable regression model was used to predict preDM/DM.
Among 187 enrolled participants, 137 (73 %) and 144 (77 %) underwent DM screening at 3 and 12 months respectively, and 137 (73 %) had imaging available. PreDM/DM occurred in 22/137 (16 %; preDM n = 21, DM n = 1) at 3 months and 23/144 (16 %; preDM n = 18, DM n = 5) participants at 12 months. Univariate associations with preDM/DM at 12 months included: severe AP (SAP) (52 % preDM/DM vs. 17 % no DM; p = 0.0008), median [IQR] IL-6 (910 pg/ml [618-3438] vs. 196 pg/ml [71-480], p < 0.05) and CRP (4.16 mg/L [1.67-10.7] vs. 1.55 mg/L [0.4-3.68], p = 0.1) at time of AP attack. The optimal multivariable model to predict preDM/DM included with clinical variables was severe acute pancreatitis (SAP), c reactive protein (CRP), interleukin-6 (IL-6), and age [AUC = 0.80; (0.70, 0.88)]. Including imaging markers, the ideal model included SAP, CRP, IL-6, subcutaneous fat area, age and presence of autoimmune disease with an AUC [0.82 (0.71, 0.90)].
Development of preDM/DM following an index AP episode can be predicted by baseline AP severity, baseline CRP, IL-6 levels, and subcutaneous fat area.
急性胰腺炎(AP)会增加患糖尿病(DM)的风险。我们的目的是确定初次发作AP后青年患者发生糖尿病前期/糖尿病的临床、实验室和影像学预测指标。
这是一项前瞻性队列研究,研究对象为年龄≤21岁的初次因AP入院且在3个月和/或12个月进行随访的患者。对初次入院时收集的临床实验室值、影像学检查结果、住院过程以及血浆趋化因子和细胞因子指标进行检测,以确定其与糖尿病前期/糖尿病发生的相关性。使用多变量回归模型预测糖尿病前期/糖尿病。
187名登记参与者中,分别有137名(73%)和144名(77%)在3个月和12个月时接受了糖尿病筛查,137名(73%)有影像学检查资料。3个月时,22/137名(16%;糖尿病前期n = 21,糖尿病n = 1)参与者发生糖尿病前期/糖尿病;12个月时,23/144名(16%;糖尿病前期n = 18,糖尿病n = 5)参与者发生糖尿病前期/糖尿病。与12个月时糖尿病前期/糖尿病的单变量相关性包括:重症急性胰腺炎(SAP)(糖尿病前期/糖尿病患者中占52%,无糖尿病患者中占17%;p = 0.0008),AP发作时白细胞介素-6(IL-6)的中位数[四分位间距](910 pg/ml [618 - 3438] 对比196 pg/ml [71 - 480],p < 0.05)和C反应蛋白(CRP)(4.16 mg/L [1.67 - 10.7] 对比1.55 mg/L [0.4 - 3.68],p = 0.1)。预测糖尿病前期/糖尿病的最佳多变量模型(包含临床变量)包括重症急性胰腺炎(SAP)、C反应蛋白(CRP)、白细胞介素-6(IL-6)和年龄[AUC = 0.80;(0.70,0.88)]。纳入影像学标志物后,理想模型包括SAP、CRP、IL-6、皮下脂肪面积、年龄和自身免疫性疾病的存在情况,AUC为[0.82(0.71,0.90)]。
初次AP发作后糖尿病前期/糖尿病的发生可通过基线AP严重程度、基线CRP、IL-6水平和皮下脂肪面积进行预测。