首页|炎症相关指标对儿童炎症性肠病的诊断价值及列线图预测模型构建

炎症相关指标对儿童炎症性肠病的诊断价值及列线图预测模型构建

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目的 分析炎症相关性指标对儿童炎症性肠病(inflammatory bowel disease,IBD)的诊断价值并构建IBD列线图预测模型.方法 选择2020年1月至2023年8月无锡市儿童医院消化内科的炎症性肠病和非炎症性肠病的患儿.比较两组患儿的一般临床资料,采用相关性分析各指标与儿童发生炎症性肠病的关联性.受试者工作特征曲线(receiver operating characteristic curve,ROC)分析单个指标和联合指标的诊断价值.通过Lasso和逐步回归法筛选出最终变量,并构建列线图预测模型.结果 本研究共纳入387例样本,其中炎症性肠病组163例,非炎症性肠病组224例.组间比较结果显示两组患者的家族史、肠道碱性磷酸酶(intestinal alkaline phosphatase,IAP)、中性粒细胞计数、C反应蛋白(C-reactive protein,CRP)、红细胞沉降率、中性粒细胞与淋巴细胞比值(neutrophil-lymphocyte count ratio,NLR)、血小板与淋巴细胞比值(platelet to lymphocyte ratio,PLR)、血小板与白蛋白比值(platelet to albumin ratio,PAR)、系统性免疫炎症指 数(systemic immune-inflammation index,SII)、淋巴细胞计数、血小板计数、白蛋白比较差异均有统计学意义(P<0.05).相关性分析结果表明家族史(r=0.199,P<0.001)、中性粒细胞计数(r=0.915,P<0.001)、红细胞沉降率(r=0.608,P<0.001)、SII(r=0.464,P<0.001)、碱性磷酸酶(r=0.491,P<0.001)、C 反应蛋白(r=0.423,P<0.001)、NLR(r=0.480,P<0.001)、PLR(r=0.353,P<0.001)、PAR(r=0.371,P<0.001)与炎症性肠病的发生呈正相关;淋巴细胞计数(r=-0.711,P<0.001)、血小板计数(r=-0.136,P=0.007)、白蛋白(r=-0.638,P<0.001)与炎症性肠病的发生呈负相关(P均<0.05).进一步ROC分析结果显示,肠道碱性磷酸酶(AUC=0.741,95%CI 0.689~0.793),C 反应蛋白(AUC=0.747,95%CI 0.690~0.804),NLR(AUC=0.781,95%CI 0.734~0.828),PLR(AUC=0.706,95%CI 0.653~0.759),PAR(AUC=0.717,95%CI 0.666~0.768),SII(AUC=0.756,95%CI 0.706~0.806)具有一定的诊断价值,各指标联合明显提高对于IBD的诊断效能(AUC=0.964,95%CI 0.946~0.982).通过碱性磷酸酶、C反应蛋白、NLR、PAR、SII、家族史、红细胞沉降率、白蛋白变量建立IBD列线图预测模型,结果显示模型C-index为0.988,提示模型具有较好的区分度,Bootstrap抽样内验证表明模型具有较高的一致性,进一步临床决策曲线分析表明该模型具有显著的临床净收益.结论 基于肠道碱性磷酸酶、C反应蛋白、NLR、PLR、PAR、SII的炎症相关指标对儿童炎症性肠病具有一定的诊断价值,各指标联合诊断价值更高.本研究构建的儿童炎症性肠病的Nomogram预测模型具有一定的临床应用价值,有利于疾病的早期筛查诊断,为临床必要的干预提供指导.
The Diagnostic Value of Inflammation Related Indicators for Inflammatory Bowel Disease in Children and the Construction of Nomogram Prediction Model
Objective To evaluate the diagnostic value of inflammation related indicators for inflammatory bowel disease(IBD)in children and to construct an IBD nomogram prediction model.Methods Children with inflammatory bowel disease and non-inflammatory bowel disease were selected from the Department of Gastroenterology at Wuxi Children's Hospital from January,2020 to August,2023.We compared the general clinical information of these two groups of children and conducted correlation analysis to examine the potential correlation between various indicators and the occurrence of inflammatory bowel disease in children.Receiver operating characteristic curve(ROC)was drawn to evaluate the diagnostic value of individual and combined indicators.We then screened the final variables through Lasso and stepwise regression,and constructed a nomogram prediction model.Results This study included a total of 387 samples,including 163 cases in the inflammatory bowel disease group and 224 cases in the non-inflammatory bowel disease group.The intergroup comparison results showed statistically significant differences in family history,alkaline phosphatase,neutrophil count,C-reactive protein,erythrocyte sedimentation rate,neutrophil lymphocyte count ratio(NLR),platelet to lymphocyte ratio(PLR),platelet to albumin ratio(PAR),systemic immune inflammation index(SII),lymphocyte count,platelet count,and albumin comparison between the two groups of patients(P<0.05).The correlation analysis showed that family history(r=0.199,P<0.001),neutrophil count(r=0.915,P<0.001),erythrocyte sedimentation rate(r=0.608,P<0.001),SII(r=0.464,P<0.001),alkaline phosphatase(r=0.491,P<0.001),C-reactive protein(r=0.423,P<0.001),NLR(r=0.480,P<0.001),PLR(r=0.353,P<0.001),and PAR(r=0.371,P<0.001)were positively correlated with the occurrence of inflammatory bowel disease;Lymphocyte count(r=-0.711,P<0.001),platelet count(r=-0.136,P=0.007),and albumin(r=-0.638,P<0.001)were negatively correlated with the occurrence of inflammatory bowel disease(all P<0.05).ROC curves showed that intestinal alkaline phosphatase(AUC=0.741,95%CI 0.689-0.793),C-reactive protein(AUC=0.747,95%CI 0.690-0.804),NLR(AUC=0.781,95%CI 0.734-0.828),PLR(AUC=0.706,95%CI 0.653-0.759),PAR(AUC=0.717,95%CI 0.666-0.768),and SII(AUC=0.756,95%CI 0.706-0.806)had certain diagnostic values,and the combination of all indicators significantly improved the diagnostic efficacy of IBD(AUC=0.706,95%CI 0.653-0.759).AUC=0.964,95%CI 0.946-0.982).A nomogram predictive model for IBD was established using alkaline phosphatase,C-reactive protein,NLR,PAR,SII,family history,erythrocyte sedimentation rate,and albumin variables.The results showed that the C-index of the model was 0.988,indicating a good discriminability.Bootstrap sampling validation showed that the model had a high consistency,and further clinical decision curve analysis showed that the model had significant clinical net benefits.Conclusion Inflammatory related indicators based on intestinal alkaline phosphatase,C-reactive protein,NLR,PLR,PAR,and SII have certain diagnostic values for pediatric inflammatory bowel disease,and the combined diagnostic value of these indicators is even higher.The nomogram prediction model for pediatric inflammatory bowel disease constructed in this study has certain clinical application values,which is beneficial for the early screening and diagnosis of the disease and can provides guidance for timely clinical interventions.

Pediatric inflammatory bowel diseaseInflammatory markersIntestinal alkaline phosphataseCombined diagnosisNomogram

黄昕昕、郝武娟、林琼

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南京医科大学附属无锡人民医院儿童消化内科,江苏无锡 214000

无锡市儿童医院消化科,江苏无锡 214000

儿童炎症性肠病 炎症指标 肠道碱性磷酸酶 联合诊断 列线图

无锡市卫健委青年项目

Q202332

2024

标记免疫分析与临床
中国同辐股份有限公司

标记免疫分析与临床

CSTPCD
影响因子:0.978
ISSN:1006-1703
年,卷(期):2024.31(9)