The Performance of Quantitative Real-Time Polymerase Chain Reaction and Galactomannan for Invasive Fungal Infections in Patients with Hematologic Malignancies
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引用次数: 0
Abstract
Background: Non-invasive methods to diagnose invasive fungal infections are needed to improve the poor outcome of these infections. We conducted this study to evaluate the diagnostic values of quantitative real time polymerase chain reaction and galactomannan in hematological malignancy patients.
Results: Eighty-two consecutive patients with cancer were identified and prospectively followed for three
months. Molecular testing using a quantitative polymerase chain reaction assay amplifying two primers 5.8S and 18S rRNA fungal genes and galactomannan was performed on 1540 blood samples and correlated with clinical data. Amplification of the 5.8S rRNA fungal gene had significantly higher sensitivity than amplification of the 18S rRNA gene for samples from either source (for blood samples: 90% vs 50%, p=0.007; for serum samples: 64% vs 5%, p<0.001).
Conclusions: Galactomannan when used alone had a sensitivity of 38% and a specificity of 100%. The
sensitivity of the combination assay of quantitative polymerase chain reaction plus galactomannan was significantly higher than that of GM test alone (71% vs 38%, p=0.03). Detection of the 5.8S rRNA fungal gene had significantly higher sensitivity than the 18S rRNA gene for samples from either source blood or serum. The combination of quantitative polymerase chain reaction plus galactomannan assay improved the diagnostic value of invasive fungal infections.
背景:需要非侵入性方法诊断侵袭性真菌感染,以改善这些感染的不良预后。我们进行这项研究是为了评估定量实时聚合酶链反应和半乳甘露聚糖在血液恶性肿瘤患者中的诊断价值。结果:确定了82例连续的癌症患者,并进行了为期3个月的前瞻性随访。采用扩增5.8S和18S rRNA真菌基因和半乳甘露聚糖两种引物的定量聚合酶链反应法对1540份血样进行分子检测,并与临床数据进行相关性分析。对于两种来源的样品,扩增5.8S rRNA真菌基因的敏感性显著高于扩增18S rRNA基因(血液样品:90% vs 50%, p=0.007;血清样本:64% vs 5%, p<0.001)。结论:半乳甘露聚糖单独使用时的敏感性为38%,特异性为100%。定量聚合酶链反应加半乳甘露聚糖联合检测的敏感性显著高于GM单独检测(71% vs 38%, p=0.03)。无论是源血还是血清,检测5.8S rRNA真菌基因的敏感性均显著高于18S rRNA基因。定量聚合酶链反应联合半乳甘露聚糖检测提高了侵袭性真菌感染的诊断价值。