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血浆PAD4、CCL19在重症肺炎并发ARDS患者中的表达及临床意义OA

Plasma PAD4 and CCL19 expression and the clinical significance in patients with severe pneumonia complicated by ARDS

中文摘要英文摘要

目的 探讨血浆肽酰基精氨酸脱亚氨酶4(PAD4)、C-C基序趋化因子配体19(CCL19)在重症肺炎(SP)并发急性呼吸窘迫综合征(ARDS)患者中的表达及临床意义.方法 按照1∶1比例前瞻性选取2020年1月—2024年12月内蒙古医科大学附属医院呼吸与危重症医学科收治的SP并发ARDS患者100例(并发ARDS组)和单纯SP患者100例(单纯SP组),根据病情程度将SP并发ARDS患者分为轻度亚组(30例)、中度亚组(36例)、重度亚组(34例),根据28 d预后将SP并发ARDS患者分为死亡亚组(41例)和存活亚组(59例).采用酶联免疫吸附法检测血浆PAD4、CCL19水平;Spearman相关分析SP并发ARDS患者血浆PAD4、CCL19水平与氧合指数(OI)的相关性;多因素Logistic回归分析SP并发ARDS患者预后死亡的影响因素;受试者工作特征(ROC)曲线分析血浆PAD4、CCL19水平对SP并发ARDS患者预后死亡的预测效能.结果 并发ARDS组血浆PAD4、CCL19水平高于单纯SP组(t/P=14.368/<0.001、17.701/<0.001);不同病情程度SP并发ARDS患者血浆PAD4、CCL19水平比较,轻度亚组<中度亚组<重度亚组(F/P=146.875/<0.001、166.125/<0.001);SP并发ARDS患者血浆PAD4、CCL19水平分别与OI呈负相关(rs/P=-0.752/<0.001、-0.744/P<0.001).SP 并发 ARDS 患者 28 d 病死率为 41.00%(41/100);PAD4 高、CCL19 高为 SP 并发 ARDS 患者预后死亡的独立危险因素[OR(95%CI)=2.710(1.567~4.684)、4.010(1.759~9.144)],OI高为独立保护因素[OR(95%CI)=0.977(0.964~0.991)];血浆PAD4、CCL19水平单独及二者联合预测SP并发ARDS患者预后死亡的曲线下面积(AUC)分别为0.814、0.795、0.909,二者联合优于血浆PAD4、CCL19水平单独预测(Z/P=2.865/0.004、2.819/0.005).结论 SP并发ARDS患者血浆PAD4、CCL19水平升高,与病情程度加重及死亡密切相关,血浆PAD4、CCL19水平联合检测对预后的预测效能较高.

Objective To investigate the expression and clinical significance of plasma peptidyl arginine deiminase 4(PAD4)and C-C motif chemokine ligand 19(CCL19)in patients with severe pneumonia(SP)complicated by acute respiratory distress syndrome(ARDS).Methods A total of 100 patients with SP complicated by ARDS(SP+ARDS group)and 100 pa-tients with SP alone(SP group)admitted to the Department of Respiratory and Critical Care Medicine of Affiliated Hospital of Inner Mongolia Medical University from January 2020 to December 2024 were prospectively enrolled in a 1∶1 ratio.Plasma PAD4 and CCL19 levels were measured by enzyme-linked immunosorbent assay.Based on oxygenation index,SP+ARDS pa-tients were further divided into mild(n=30),moderate(n=36),and severe(n=34)ARDS subgroups.Spearman correlation analysis was used to evaluate the association between PAD4,CCL19 levels and oxygenation index.Patients were also classi-fied into survival and death groups based on 28-day outcomes.Multivariate Logistic regression was performed to analyze fac-tors affecting prognosis.Receiver operating characteristic(ROC)curves were used to assess the predictive value of plasma PAD4 and CCL19 levels for prognosis.Results Compared with the SP group,plasma PAD4 and CCL19 levels were significantly higher in the SP+ARDS group(t/P=14.368/<0.001,17.701/<0.001).In SP patients with ARDS,plasma PAD4 and CCL19 lev-els increased progressively from mild to moderate to severe subgroups(F/P=146.875/<0.001,166.125/<0.001).Plasma PAD4 and CCL19 levels were negatively correlated with oxygenation index(rs/P=-0.752/<0.001,-0.744/<0.001).The 28-day mor-tality rate in SP patients with ARDS was 41.00%(41/100).Increased oxygenation index was an independent protective factor for poor prognosis,while elevated PAD4 and CCL19 levels were independent risk factors[OR(95%CI)=0.977(0.964-0.991),2.710(1.567-4.684),4.010(1.759-9.144)].The AUCs for plasma PAD4,CCL19,and their combination in predicting poor prognosis were 0.814,0.795,and 0.909,respectively;the combined model outperformed either biomarker alone(Z/P=2.865/0.004,2.819/0.005).Conclusion Elevated plasma PAD4 and CCL19 levels in SP patients with ARDS are closely associated with greater disease severity and higher mortality.The combination of plasma PAD4 and CCL19 levels provides superior pre-dictive value for prognosis compared with either marker alone.

郭倩茹;吴洁;年英;段智慧;朱天吉

010100 呼和浩特,内蒙古医科大学附属医院呼吸与危重症医学科010100 呼和浩特,内蒙古医科大学附属医院呼吸与危重症医学科010100 呼和浩特,内蒙古医科大学附属医院呼吸与危重症医学科010100 呼和浩特,内蒙古医科大学附属医院呼吸与危重症医学科010100 呼和浩特,内蒙古医科大学附属医院呼吸与危重症医学科

医药卫生

重症肺炎急性呼吸窘迫综合征肽酰基精氨酸脱亚氨酶4C-C基序趋化因子配体19病情程度预后

Severe pneumoniaAcute respiratory distress syndromePeptidyl arginine deiminase 4C-C motif che-mokine ligand 19Disease severityPrognosis

《疑难病杂志》 2026 (1)

48-53,6

内蒙古自治区医疗卫生科技计划项目(202201047) Inner Mongolia Autonomous Region Medical and Health Science and Technology Plan Project(202201047)

10.3969/j.issn.1671-6450.2026.01.009

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