血清ANXA1、CLDN18水平与支气管哮喘患儿临床分期、急性期病情严重程度及气道炎症的关系OA
Relationship between serum ANXA1 and CLDN18 levels with clinical stage,acute stage severity and airway inflammation in children patients with bronchial asthma
目的 分析血清膜联蛋白 A1(ANXA1)、封闭蛋白18(CLDN18)与支气管哮喘(BA)患儿临床分期、急性期病情严重程度及气道炎症的关系.方法 选取2023年1月至2024年12月该院收治的BA急性期患儿240例(急性期组)和BA缓解期患儿80例(缓解期组)作为研究对象,BA急性期患儿根据病情严重程度分为轻度BA急性期组96例、中度BA急性期组84例、重度BA急性期组60例.另选取同期在该院体检的健康儿童80例作为对照组.比较各组血清ANXA1、CLDN18水平,以及外周血嗜酸性粒细胞(EOS)计数、肺功能指标[峰值呼气流速(PEF)和第1秒用力呼气容积占预计值百分比(FEV1%pred)]和呼出气一氧化氮(FeNO)水平;采用Pearson或Spearman相关进行相关性分析;采用多因素Logistic回归分析BA分期的关联因素;采用有序多分类Logistic回归分析BA急性期患儿病情严重程度的关联因素;绘制受试者工作特征(ROC)曲线分析血清ANXA1、CLDN18判断 BA 处于急性期及重度 BA 急性期的价值.结果 急性期组血清 ANXA1、CLDN18水平均高于对照组、缓解期组(P<0.017),缓解期组血清 ANXA1、CLDN18水平均高于对照组(P<0.017).急性期组PEF、FEV1%pred均低于对照组、缓解期组(P<0.017),EOS计数、FeNO水平均高于对照组、缓解期组(P<0.017);缓解期组PEF、FEV1%pred均低于对照组(P<0.017),EOS计数、FeNO水平均高于对照组(P<0.017).重度BA 急性期组PEF、FEV1%pred均低于轻度BA 急性期组、中度BA 急性期组(P<0.017),EOS计数、FeNO水平及血清ANXA1、CLDN18水平均高于轻度BA急性期组、中度BA急性期组(P<0.017);中度BA急性期组PEF、FEV1%pred均低于轻度BA急性期组(P<0.017),EOS计数、FeNO水平及血清ANXA1、CLDN18水平均高于轻度BA急性期组(P<0.017).BA急性期患儿血清 ANXA1水平与病情严重程度、EOS计数、FeNO水平呈正相关(rs/r=0.774、0.513、0.651,均P<0.001),与PEF、FEV1%pred呈负相关(r=-0.570、-0.724,均P<0.001);血清CLDN18水平与病情严重程度、EOS计数、FeNO水平呈正相关(rs/r=0.784、0.456、0.582,均P<0.001),与 PEF、FEV1%pred均呈负相关(r=-0.567、-0.696,均P<0.001);病情严重程度与PEF、FEV1%pred呈负相关(rs=-0.708、-0.757,均P<0.001),与EOS计数、FeNO水平呈正相关(rs=0.668、0.737,均P<0.001).PEF升高、FEV1%pred升高均与BA处于急性期的可能性降低相关(P<0.05),EOS计数升高、FeNO 水平升高、血清 ANXA1水平升高、血清CLDN18水平升高均与BA急性期的可能性增加相关(P<0.05).PEF升高、FEV1%pred升高均与BA急性期患儿病情加重的可能性降低相关(P<0.05),EOS计数升高、FeNO水平升高、血清 ANXA1水平升高、血清CLDN18水平升高均与BA急性期患儿病情加重的可能性增加相关(P<0.05).血清 ANXA1、CLDN18单独及联合判断BA处于急性期的曲线下面积(AUC)分别为0.798、0.813、0.887,2项联合判断的 AUC大于血清ANXA1、CLDN18单独判断(Z=3.817、3.718,均P<0.001).血清 ANXA1、CLDN18单独及联合判断重度BA急性期的AUC分别为0.783、0.796、0.897,2项联合判断的AUC大于血清ANXA1、CLDN18单独判断(Z=4.541、3.824,均P<0.001).结论 BA急性期患儿血清ANXA1、CLDN18水平升高,2项与BA急性期患儿病情严重程度、气道炎症加重及肺功能降低有关,且2项联合判断BA处于急性期及重度BA急性期的价值较高.
Objective To analyze the relationship between serum annexin A1(ANXA1)and claudin 18(CLDN18)with the clinical stage,severity in the acute stage and airway inflammation in children patients with bronchial asthma(BA).Methods A total of 240 children patients with acute stage of BA(acute stage group)and 80 children patients with remission stage of BA(remission stage group)admitted and treated in this hospital from January 2023 to December 2024 were selected as the research subjects.The children patients with acute phase of BA were divided into the mild acute BA group(96 cases),moderate acute BA group(84 cases)and severe acute BA group(60 cases)based on the disease severity.The other 80 healthy children who underwent physical examinations in this hospital during the same period were selected as the control group.The serum ANXA1 and CLDN18 levels,eosinophil count in peripheral blood,lung function indicators[peak expiratory flow(PEF)and forced expiratory volume in one second as a percentage of predicted value(FEV1%pred)],and fractional exhaled nitric oxide(FeNO)levels were compared among the groups.Pearson or Spearman correlation analysis was used to conduct the correlation analysis.The multivariate Logistic regres-sion was used to analyze the associated factors of BA stages,and the ordered multinomial Logistic regression was used to analyze the associated factors of the severity in the children patients with acute BA.The receiver operating characteristic(ROC)curves were drawn to analyze the value of serum ANXA1 and CLDN18 in jud-ging the acute stage and severe acute stage of BA.Results The serum ANXA1 and CLDN18 levels in the a-cute phase group were higher than those in the control group and remission phase group(P<0.017),and the serum ANXA1 and CLDN18 levels in the remission phase group were higher than those in the control group(P<0.017).The PEF and FEV1%pred in the acute phase group were lower than those in the control group and remission phase group(P<0.017),and the eosinophil count and FeNO level were higher than those in the control group and remission phase group(P<0.017);the PEF and FEV1%pred in the remission phase group were lower than those in the control group(P<0.017),and the eosinophil count and FeNO level were higher than those in the control group(P<0.017).The PEF and FEV1%pred in the severe acute stage BA group were lower than those in the mild acute stage BA group and the moderate acute stage BA group(P<0.017),and the eosinophil count,FeNO levels and serum ANXA1 and CLDN18 levels were higher than those in the mild acute stage BA group and moderate acute stage BA group(P<0.017);the PEF and FEV1%pred in the moderate acute stage BA group were lower than those in the mild acute stage BA group(P<0.017),and the eosinophil count,FeNO levels,and serum ANXA1 and CLDN18 levels were higher than those in the mild acute stage BA group(P<0.017).The serum ANXA1 level in children patients with acute stage BA was positively correlated with the severity degree of the disease,eosinophil count and FeNO level(rs/r=0.774,0.513,0.651;all P<0.001),and negatively correlated with PEF and FEV1%pred(r=-0.570,-0.724;both P<0.001);the serum CLDN18 level was positively correlated with the severity degree of the disease,eosino-phil count and FeNO level(rs/r=0.784,0.456,0.582;all P<0.001),and negatively correlated with PEF and FEV1%pred(r=-0.567,-0.696;both P<0.001).The severity degree of the disease was negatively corre-lated with PEF and FEV1%pred(rs=-0.708,-0.757;both P<0.001),and positively correlated with EOS count and FeNO level(rs=0.668,0.737;both P<0.001).The increased PEF and increased FEV1%pred were both correlated with reduced likelihood of BA being in the acute stage(P<0.05),while the increased EOS count,increased FeNO level,increased serum ANXA1 level and increased serum CLDN18 level were all correlated with reduced likelihood of BA being in the acute stage(P<0.05).The increased PEF and increased FEV1%pred were both correlated with reduced likelihood of disease aggravation in children patients with a-cute stage of BA(P<0.05),while the increased EOS count,increased FeNO level,increased serum ANXA1 level and increased serum CLDN18 level were all correlated with increased likelihood of disease aggravation in children patients with acute stage of BA(P<0.05).The areas under the curves(AUCs)of serum ANXA1,CLDN18 alone and their combination for judging the acute stage in BA were 0.798,0.813 and 0.887,respec-tively.The AUC of the 2-item combination judgment was greater than that of serum ANXA1 and CLDN18 a-lone(Z=3.817,3.718;both P<0.001).The AUCs of serum ANXA1,CLDN18 alone and their combination judgment for the acute stage in severe BA were 0.783,0.796,and 0.897,respectively.The AUC of the 2-item combination judgment was greater than that of serum ANXA1 and CLDN18 alone(Z=4.541,3.824;both P<0.001).Conclusion The serum ANXA1 and CLDN18 levels are increased in children patients with acute stage of BA.These two indicators are related to the severity degree of the disease,aggravation of airway in-flammation and lung function reduction in children patients with acute stage of BA.Moreover,the value of the 2-item combination for judging BA in the acute stage and the acute stage of severe BA is relatively high.
李湘萍;刘建华;刘世英
甘肃省武威市人民医院:儿科,甘肃 武威 733099甘肃省武威市人民医院:儿科,甘肃 武威 733099甘肃省武威市人民医院:新生儿科,甘肃 武威 733099
医药卫生
支气管哮喘膜联蛋白A1封闭蛋白18病情严重程度肺功能气道炎症儿童
bronchial asthmaannexin A1claudin-18disease severity degreelung functionairway inflammationchildren
《检验医学与临床》 2026 (10)
1297-1305,9
甘肃省卫生健康行业科研项目(GSWSKY2020-30)甘肃省武威市科技计划项目(WW23B02SF016).
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