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作 者:关岳 李新 杨贺旻 徐思宇 史丽东 刘扬洋 孔令丹 秦影 GUAN Yue;LI Xin;YANG He-min;XU Si-yu;SHI Li-dong;LIU Yang-yang;KONG Ling-dan;QIN Ying(Department of rheumatology and immunology,the Third Affi liated Hospital of Qiqihar Medical University,Qiqihar Heilongjiang,161006,China;Central Laboratory,the Third Affi liated Hospital of Qiqihar Medical University,Qiqihar Heilongjiang,161006,China;Inspection Center,the Third Affi liated Hospital of Qiqihar Medical University,Qiqihar Heilongjiang,161006,China)
机构地区:[1]黑龙江省齐齐哈尔医学院附属第三医院风湿免疫科,黑龙江齐齐哈尔161006 [2]黑龙江省齐齐哈尔医学院附属第三医院中心实验室,黑龙江齐齐哈尔161006 [3]黑龙江省齐齐哈尔医学院附属第三医院检验中心,黑龙江齐齐哈尔161006
出 处:《中华养生保健》2024年第19期4-8,共5页CHINESE HEALTH CARE
基 金:2023年黑龙江省省属本科高校基本科研业务费项目(2023-KYYWF-0878)。
摘 要:目的探究干扰素调节因子9(IRF9)、蛋白酶体a5亚基(PSMA5)联合外周血巨噬细胞经典激活(M1)和替代激活(M2)极化状态对类风湿性关节炎(RA)进展的预测价值。方法选取2022年2月—2023年2月齐齐哈尔医学院附属第三医院收治的87例RA患者,根据疾病严重程度将其分为活动期组和缓解期组。比较两组患者IRF9、PSMA5、M1/M2比值,采用二元Logistic回归分析其与RA进展的关系,构建风险预测模型,利用ROC曲线、校准曲线与决策曲线评价其预测价值。结果缓解期组共49例患者(56.32%),活动期组共38例患者(43.68%),两组在累及关节数、关节压痛指数及关节肿胀指数等方面,差异有统计学意义(P<0.05);活动期患者IRF9、PSMA5、M1、M1/M2比例显著高于缓解期组,但M2显著低于缓解期组,差异有统计学意义(P<0.05);Logistic回归分析显示IRF9、PSMA5、M1/M2比值是RA疾病进展的危险因素;ROC分析用于预测RA进展,AUC值显示M1/M2为0.690,IRF9为0.664,PSMA5为0.733。结论M1/M2、IRF9、PSMA5与RA疾病进展相关,有助于评估RA疾病进展。Objective To study the predictive value of IRF9 and PSMA5 combined with M1 and M2 macrophage polarization on rheumatoid arthritis(RA)progression.Methods A total of 87 RA patients were divided into active and remission groups based on disease severity.IRF9 and PSMA5 expression,M1 and M2 macrophage proportions,and the M1/M2 ratio were compared.Logistic regression and ROC analysis were used to assess predictive performance.Results Higher expression of IRF9 and PSMA5 was seen in active RA patients.M1/M2 ratio was higher in active RA.Logistic regression identifi ed IRF9,PSMA5,and M1/M2 ratio as RA progression risk factors.AUC values for predicting RA progression were 0.690 for M1/M2,0.664 for IRF9,and 0.733 for PSMA5.Conclusion M1/M2 polarization,IRF9,and PSMA5 levels were elevated in RA patients and correlated with disease progression.These markers could be valuable for assessing and evaluating RA progression clinically.
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