切换至 "中华医学电子期刊资源库"

中华消化病与影像杂志(电子版) ›› 2025, Vol. 15 ›› Issue (03) : 250 -255. doi: 10.3877/cma.j.issn.2095-2015.2025.03.012

论著

SIGIRR、IL-1、Treg/Th17、NLR与急性胰腺炎继发脓毒症病情程度及预后的关联性
王浩1, 黄咪2, 李雪琴1,()   
  1. 1. 725000 陕西省,安康市人民医院重症医学科
    2. 725000 陕西省,安康市人民医院消化内科
  • 收稿日期:2025-01-18 出版日期:2025-06-01
  • 通信作者: 李雪琴

Correlation of SIGIRR, IL-1, Treg/Th17, NLR with severity and prognosis of acute pancreatitis secondary sepsis

Hao Wang1, Mi Huang2, Xueqin Li1,()   

  1. 1. Department of Critical Care Medicine,Ankang People's Hospital, Ankang 725000, China
    2. Department of Gastroenterology, Ankang People's Hospital, Ankang 725000, China
  • Received:2025-01-18 Published:2025-06-01
  • Corresponding author: Xueqin Li
引用本文:

王浩, 黄咪, 李雪琴. SIGIRR、IL-1、Treg/Th17、NLR与急性胰腺炎继发脓毒症病情程度及预后的关联性[J/OL]. 中华消化病与影像杂志(电子版), 2025, 15(03): 250-255.

Hao Wang, Mi Huang, Xueqin Li. Correlation of SIGIRR, IL-1, Treg/Th17, NLR with severity and prognosis of acute pancreatitis secondary sepsis[J/OL]. Chinese Journal of Digestion and Medical Imageology(Electronic Edition), 2025, 15(03): 250-255.

目的

分析外周血单免疫球蛋白白细胞介素1 受体相关蛋白(SIGIRR)、白细胞介素-1(IL-1)、调节性T 细胞(Treg)/辅助性T 细胞17(Th17)比值、中性粒细胞/淋巴细胞比值(NLR)与急性胰腺炎患者病情程度及预后的关联性。

方法

回顾性分析2021 年1 月至2024 年1 月安康市人民医院收治的120 例急性胰腺炎患者的临床资料,根据患者病情严重程度分为两组,继发脓毒症组56 例,未继发脓毒症组64 例,另选取同期健康体检者50 例为对照组,随访1 个月,根据患者预后情况,将其分为生存组86 例,死亡组34 例,收集所有受试者的外周血内SIGIRR、IL-1、Treg/Th17、NLR 等资料,比较不同组别患者间的指标水平差异,使用Spearman 分析外周血内SIGIRR、IL-1、Treg/Th17、NLR 与急性胰腺炎继发脓毒症患者病情程度及预后的关联性;采用Logistic 多因素回归模型,评估效能绘制受试者工作特征(ROC)曲线,计算曲线下面积(AUC)评估各指标对急性胰腺炎继发脓毒症预后的预测价值。

结果

急性胰腺炎继发脓毒症组SIGIRR、IL-1、Treg/Th17、NLR水平均高于未继发脓毒症组、对照组,未继发脓毒症组各指标水平均高于对照组(P<0.05),死亡组SIGIRR、IL-1、Treg/Th17、NLR 水平均高于生存组(P<0.05)。单因素及Logistic 多因素回归分析显示,SIGIRR≥80.45 pg/L、IL-1≥576.54 ng/L、Treg/Th17≥0.26、NLR≥10.14 均为预测急性胰腺炎继发脓毒症患者预后的危险因素(P<0.05)。ROC 曲线显示,SIGIRR 的AUC 最高(0.856,95% CI 0.810~0.902),Treg/Th17 次之(0.841,95% CI 0.793~0.889),四项指标联合的AUC 达0.886(95% CI 0.828~0.931),显著高于任一单一指标(Delong 检验,P<0.05)。联合模型的敏感度为84.4%,特异度为86.7%。

结论

外周血SIGIRR、IL-1、Treg/Th17 和NLR 在急性胰腺炎继发脓毒症患者病情程度及预后呈显著相关,四项指标联合检测具有优异的预测效能,同时监测有助于反映临床诊疗和预后评估。

Objective

To investigate the associations between single Ig interleukin-1-related receptor (SIGIRR), interleukin-1 (IL-1), regulatory T cells (Treg)/helper T cell 17 (Th17) and neutrophil/lymphocyte ratio (NLR) and the severity and prognosis of patients with acute pancreatitis.

Methods

The clinical data of 120 patients with acute pancreatitis admitted to Ankang People's Hospital from January 2021 to January 2024 were retrospectively analyzed.According to the severity of the patients' conditions,they were divided into two groups: 56 patients in the secondary sepsis group and 64 patients in the non-secondary sepsis group, and 50 healthy patients with physical examination during the same period were selected as the control group.The patients were followed up for 1 month.According to the prognosis of the patients, they were divided into a survival group (86 cases) and a death group (34 cases).SIGIRR,IL-1, Treg/Th17, NLR and other data in peripheral blood of all subjects were collected, and the difference of indicator levels among different groups of patients was compared.Spearman was used to analyze the correlation between SIGIRR, IL-1, Treg/Th17 and NLR in peripheral blood and the severity and prognosis of patients with acute pancreatitis secondary sepsis.Logistic multi-factor regression model was used to evaluate the performance.Receiver operating characteristic (ROC) curve was drawn and the area under the curve was calculated to evaluate the prognostic value of each index in acute pancreatitis secondary sepsis.

Results

The levels of SIGIRR, IL-1, Treg/Th17 and NLR in acute pancreatitis secondary sepsis group were higher than those in non-secondary sepsis group and control group, and the levels of all indexes in non-secondary sepsis group were higher than those in control group (P<0.05).The levels of SIGIRR, IL-1,Treg/Th17 and NLR in the death group were all higher than those in the survival group (P<0.05).Univariate and Logistic multivariate regression analyses showed that SIGIRR≥80.45 pg/L, IL-1≥576.54 ng/L, Treg/Th17≥0.26, and NLR≥10.14 were all risk factors for predicting the prognosis of patients with secondary sepsis due to acute pancreatitis (P<0.05).The ROC curve showed that the AUC of SIGIRR was the highest (0.856, 95% CI 0.810-0.902), followed by Treg/Th17 (0.841, 95% CI 0.793-0.889), the combined AUC of the four indicators reached 0.886 (95% CI 0.828-0.931), which was significantly higher than that of any single indicator (Delong test, P<0.05), the sensitivity of the combined model was 84.4%and the specificity was 86.7%.

Conclusion

Peripheral blood SIGIRR, IL-1, Treg/Th17 and NLR are significantly correlated with the severity and prognosis of patients with secondary sepsis due to acute pancreatitis.The combined detection of the four indicators has excellent predictive efficacy.Meanwhile,monitoring is helpful to reflect clinical diagnosis and treatment as well as prognosis assessment.

表1 不同病情严重程度患者与健康对照组临床资料比较(±s
表2 不同预后急性胰腺炎患者各指标比较(±s
表3 急性胰腺炎继发脓毒症患者预后的预测风险因素单因素和多因素回归分析
图1 多因素预测急性胰腺炎继发脓毒症患者预后的ROC 曲线 注:SIGIRR 单免疫球蛋白白细胞介素1 受体相关蛋白;IL-1 白细胞介素-1;Treg/Th17 调节性T 细胞/辅助性T 细胞17 比值;NLR 中性粒细胞/淋巴细胞比值
表4 SIGIRR、IL-1、Treg/Th17、NLR 预测急性胰腺炎继发脓毒症患者预后的效能分析
[1]
Sohail Z, Shaikh H, Iqbal N, et al.Acute pancreatitis: A narrative review[J].J Pak Med Assoc, 2024, 74(5): 953-958.
[2]
彭凯新, 文礼.急性胰腺炎的发病机制研究进展及未来展望[J].西安交通大学学报(医学版), 2024, 45(2): 167-177.
[3]
Zerem E, Kurtcehajic A, Kunosić S, et al.Current trends in acute pancreatitis: Diagnostic and therapeutic challenges[J].World J Gastroenterol, 2023, 29(18): 2747-2763.
[4]
Hu Y, Ding J, Chen Y, et al.Soluble Fibrinogen-Like Protein 2 Downregulation and Th17/Treg Imbalance in a Taurocholate-Induced Murine Experimental Model of Severe Acute Pancreatitis[J].J Clin Lab Anal, 2024, 38(10): e25076.
[5]
Yue X, Lai L, Wang R, et al.DGA ameliorates severe acute pancreatitis through modulating macrophage pyroptosis[J].Inflamm Res, 2024, 73(10): 1803-1817.
[6]
中华医学会外科学分会胰腺外科学组.中国急性胰腺炎诊治指南(2021)[J].浙江实用医学, 2021, 26(6): 511-519+535.
[7]
Zhang C, Li G, Lu T, et al.The Interaction of Microbiome and Pancreas in Acute Pancreatitis[J].Biomolecules, 2023, 14(1): 59.
[8]
李思思, 何强, 徐有青.全身炎症反应指数对急性胰腺炎患者严重程度的评估价值研究[J].中国全科医学, 2024, 27(17): 2104-2108.
[9]
Wang C, Zhang J, Liu L, et al.EARLY PREDICTIVE VALUE OF PRESEPSIN FOR SECONDARY SEPSIS AND MORTALITY IN INTENSIVE CARE UNIT PATIENTS WITH SEVERE ACUTE PANCREATITIS[J].Shock, 2023, 59(4): 560-568.
[10]
张学英, 杜娟娟, 张菊, 等.老年急性胰腺炎患者的临床和CT 特征[J].中国医学计算机成像杂志, 2024, 30(4): 451-456.
[11]
Beyer G, Hoffmeister A, Lorenz P, et al.Clinical Practice Guideline—Acute and Chronic Pancreatitis[J].Dtsch Arztebl Int,2022, 119(29-30): 495-501.
[12]
Zhang Y, Cui YF.Severe acute pancreatitis complicated with intra-abdominal infection secondary to trauma: A case report[J].World J Clin Cases, 2024, 12(25): 5821-5831.
[13]
Shuanglian Y, Huiling Z, Xunting L, et al.Establishment and validation of early prediction model for hypertriglyceridemic severe acute pancreatitis[J].Lipids Health Dis, 2023, 22(1): 218.
[14]
Anılır E, Özen F, Yıldırım İH.Effects of toll like receptor 4(TLR4)and toll like receptor 2(TLR 2) gene polymorphisms on clinical outcomes in acute non-biliary pancreatitis patients[J].Front Immunol, 2024, 15: 1427187.
[15]
Wan L, Lin KT, Rahman MA, et al.Splicing Factor SRSF1 Promotes Pancreatitis and KRASG12D-Mediated Pancreatic Cancer[J].Cancer Discov, 2023, 3(7): 1678-1695.
[16]
Wang Z, Liu J, Li F, et al.Mechanisms of Qingyi Decoction in Severe Acute Pancreatitis-Associated Acute Lung Injury via Gut Microbiota: Targeting the Short-Chain Fatty Acids-Mediated AMPK/NFκB/NLRP3 Pathway[J].Microbiol Spectr, 2023, 11(4): e0366422.
[17]
Yang X, Li R, Xu L, et al.Serum amyloid A3 is required for caerulein-induced acute pancreatitis through induction of RIP3-dependent necroptosis[J].Immunol Cell Biol, 2021, 99(1): 34-48.
[18]
Liu J, Huang Y, Liu N, et al.The imbalance of pulmonary Th17/Treg cells in BALB/c suckling mice infected with respiratory syncytial virus-mediated intestinal immune damage and gut microbiota changes[J].Microbiol Spectr, 2024, 12(6): e0328323.
[19]
魏晓梅, 叶丰进.基于TLR4/NF-κB 信号通路探讨大黄素对急性胰腺炎大鼠Th17/Treg 平衡及炎症反应的影响[J].广东药科大学学报, 2024, 40(5): 15-19.
[20]
Lu F, Zhang Y, Yu J, et al.Clinical value of BISAP score combined with CRP and NLR in evaluating the severity of acute pancreatitis[J].Medicine(Baltimore), 2023, 102(45): e35934.
[21]
秦永军, 刘瑾, 李盛, 陈斌.急性胰腺炎患者入院24h 内外周血AFR、NLR、AMY 水平变化及临床意义[J].中南医学科学杂志,2023, 51(6): 908-911.
[22]
崔秋子, 姚红曼, 艾迎春.监测NLR、PLR、CAR、白蛋白、血钙及血糖指标水平对急性胰腺炎患者急性肾损伤的预测价值分析[J/OL].中华消化病与影像杂志(电子版), 2024, 14(3): 244-248.
[23]
Yee KX, Lee YC, Nguyen HD, et al.Uncovering the role of FXYD3 as a potential oncogene and early biomarker in pancreatic cancer[J].Am J Cancer Res, 2024, 14(9): 4353-4366.
[24]
Lu F, Zhang Y, Yu J, et al.Clinical value of BISAP score combined with CRP and NLR in evaluating the severity of acute pancreatitis[J].Medicine(Baltimore), 2023, 102(45): e35934.
[25]
Hu Y, Ding J, Chen Y, Wang Q, et al.Soluble Fibrinogen-Like Protein 2 Downregulation and Th17/Treg Imbalance in a Taurocholate-Induced Murine Experimental Model of Severe Acute Pancreatitis[J].J Clin Lab Anal, 2024, 38(10): e25076.
[26]
Peng Y, Yang Y, Li Y, et al.Mitochondrial(mt)DNA-cyclic GMP-AMP synthase(cGAS)-stimulator of interferon genes(STING)signaling promotes pyroptosis of macrophages via interferon regulatory factor(IRF)7/IRF3 activation to aggravate lung injury during severe acute pancreatitis[J].Cell Mol Biol Lett, 2024, 29(1): 61.
[27]
Jain V, Nath P, Patro S.Evaluation of diagnostic accuracy of inflammation markers[Neutrophil-Lymphocyte Ratio(NLR), Red cell Distribution Width(RDW), Prognostic Nutritional Index(PNI) and Lymphocyte Monocyte Ratio(LMR)] for outcomes in patients with acute pancreatitis[J].J Assoc Physicians India, 2022, 70(4): 11-12.
[1] 陈瑞, 王丽, 徐海乐, 许彬, 陈超, 陆件. 早期监测白细胞介素35 联合肝素结合蛋白对脓毒症相关急性肾损伤的预测价值[J/OL]. 中华危重症医学杂志(电子版), 2025, 18(02): 122-127.
[2] 黄敏, 代大华, 黄红梅, 付豹, 傅小云. 糖尿病酮症酸中毒并发急性胰腺炎患者的临床特征及预后分析[J/OL]. 中华危重症医学杂志(电子版), 2025, 18(01): 5-10.
[3] 贾艳慧, 原毅轩, 官浩, 胡大海. 清除衰老细胞在减轻脓毒症小鼠急性肺损伤中的作用机制探讨[J/OL]. 中华损伤与修复杂志(电子版), 2025, 20(01): 55-60.
[4] 唐浩然, 周彪, 巴特, 李洋洋. 严重烧伤后脓毒症早期诊断相关生物标记物的研究进展[J/OL]. 中华损伤与修复杂志(电子版), 2025, 20(01): 70-74.
[5] 王鹏森, 吴慧锋, 温建芳, 韦阳, 董龙浩, 刘博强, 李占, 石春锋, 雷晓栋, 吴雄雄. 脓毒症并发急性肺损伤血清miR-146a 的表达及与预后相关性分析[J/OL]. 中华肺部疾病杂志(电子版), 2025, 18(02): 241-245.
[6] 宗晓龙, 林源希, 张天翼, 刘雅茹, 李端阳, 李真玉. 紫檀芪通过抑制炎症反应和NETs 形成对减轻脓毒症小鼠急性肺损伤的影响[J/OL]. 中华肺部疾病杂志(电子版), 2025, 18(01): 29-35.
[7] 兰永, 刘晶, 杨志琦, 吴浪, 沙小春, 李明皓. 肠道菌群在胰腺炎发生发展中的研究进展[J/OL]. 中华肝脏外科手术学电子杂志, 2025, 14(03): 481-486.
[8] 李菲, 郭晓夏, 郑悦, 郑爔, 李鑫成, 李文雄. 他汀类药物对甘油三酯葡萄糖指数增高的脓毒症相关急性肾损伤患者预后的影响[J/OL]. 中华肾病研究电子杂志, 2025, 14(02): 68-76.
[9] 吴健锋, 裴飞, 管向东. 严重感染与免疫功能障碍:2024年度进展与展望[J/OL]. 中华重症医学电子杂志, 2025, 11(01): 27-30.
[10] 王冉, 常炜, 杨毅, 徐静媛. 脓毒症休克液体复苏的晶体液种类对急性肾损伤影响的研究进展[J/OL]. 中华重症医学电子杂志, 2025, 11(01): 100-104.
[11] 尚伟锋, 陈德昌. 基于肠道菌群探讨脓毒症相关脑病治疗的新靶点[J/OL]. 中华重症医学电子杂志, 2025, 11(01): 31-35.
[12] 吴娟娟, 武海龙. 监测术前NLR、PLR 及SII 水平对全身麻醉下结直肠癌根治术后并发肠梗阻的预测价值[J/OL]. 中华消化病与影像杂志(电子版), 2025, 15(03): 214-218.
[13] 欧阳慧, 张志红, 袁玉军, 鲁石. 早期血常规、凝血功能指标与急性胰腺炎患者螺旋CT 灌注参数的关联性及对预后的指导价值[J/OL]. 中华消化病与影像杂志(电子版), 2025, 15(02): 107-111.
[14] 刘杰, 马毛毛, 高星星. 轻度胃肠炎伴婴幼儿良性惊厥患儿肠道菌群特征与血清NSE、NO、IL-1、IL-6 的关系[J/OL]. 中华消化病与影像杂志(电子版), 2025, 15(02): 168-173.
[15] 李兆蕾, 詹敏金, 陈海天. 妊娠合并高甘油三酯血症性急性胰腺炎的临床研究[J/OL]. 中华产科急救电子杂志, 2025, 14(02): 86-94.
阅读次数
全文


摘要


AI


AI小编
你好!我是《中华医学电子期刊资源库》AI小编,有什么可以帮您的吗?