鸟苷酸结合蛋白5基因诊断结核分枝杆菌感染的临床价值

Clinical value of guanylate binding protein 5 gene in diagnosis of Mycobacterium tuberculosis infection

  • 摘要:
    目的 探讨鸟苷酸结合蛋白5(GBP5)基因对结核分枝杆菌(MTB)感染患者的诊断价值。
    方法 选取2024年1-5月在苏州市第五人民医院就诊的患者, 及同期进行健康体检的人群为研究对象。根据诊断标准将研究对象分为活动性肺结核(ATB)组230例、肺炎组207例、结核潜伏性感染(LTBI)组48例和健康对照(HC)组122例, 使用实时定量反转录聚合酶链式反应技术检测受试者全血中GBP5基因表达水平, 采用受试者工作特征(ROC)曲线分析其诊断性能。
    结果 四组GBP5基因差异有统计学意义(P<0.001), GBP5区分ATB组与HC组、LTBI组及肺炎组的ROC曲线下面积(AUC)分别为0.902、0.813及0.745。在ATB组中, GBP5方法的阳性检出率为67.39%, 高于Gene Xpert MTB/RIF(62.20%)、结核培养(60.00%)和涂片抗酸染色(35.20%)(P<0.05)。区分ATB和LTBI患者时, GBP5的阳性预测值为95.09%, 高于IGRA检测(79.92%)(P<0.05)。GBP5表达量与MTB菌量负荷呈负相关(P<0.001)。
    结论 GBP5基因检测在结核病的辅助诊断中具有重要的临床意义, 可作为现有结核病诊断方法的有效补充。

     

    Abstract:
    OBJECTIVE To explore the diagnostic value of the guanylate binding protein 5 (GBP5) gene in patients infected with Mycobacterium tuberculosis (MTB).
    METHODS Patients who visited the Fifth People′s Hospital of Suzhou from Jan. 2024 to May 2024, as well as individuals undergoing health examinations during the same period, were selected as the study subjects. Based on the diagnostic criteria, the subjects were divided into active tuberculosis (ATB) group (230 cases), pneumonia group (207 cases), latent tuberculosis infection (LTBI) group (48 cases) and healthy control (HC) group (122 cases). Real-time quantitative reverse transcription polymerase chain reaction was used to detect the expression level of the GBP5 gene in the whole blood of the subjects, and receiver operating characteristic (ROC) curves were employed to analyze its diagnostic performance.
    RESULTS There were statistically significant differences in GBP5 gene expression among the four groups (P < 0.001). The area under the ROC curve (AUC) for GBP5 in distinguishing the ATB group from the HC group, LTBI group and pneumonia group was 0.902, 0.813 and 0.745, respectively. In the ATB group, the positive detection rate of the GBP5 method was 67.39%, higher than that of Gene Xpert MTB/RIF (62.20%), tuberculosis culture (60.00%) and smear acid-fast staining (35.20%) (P < 0.05). When distinguishing between ATB and LTBI patients, the positive prediction value of GBP5 was 95.09%, higher than that of IGRA testing (79.92%) (P < 0.05). The expression level of GBP5 was negatively correlated with the MTB bacterial load (P < 0.001).
    CONCLUSIONS The detection of the GBP5 gene has important clinical significance in the auxiliary diagnosis of tuberculosis and can serve as an effective supplement to existing diagnostic methods for tuberculosis.

     

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