Laboratoire de Parasitologie-Mycologie, Groupe Hospitalier Lariboisière, Saint-Louis, Fernand Widal, Assistance Publique-Hôpitaux de Paris (AP-HP), 75010 Paris, France.
Université de Paris, 75006 Paris, France.
Med Mycol. 2021 Sep 3;59(9):882-889. doi: 10.1093/mmy/myab016.
Serum (1→3)-β-D-glucan (BDG), an pan fungal antigen, is detected in some invasive fungal diseases (IFDs). We compared two commercial kits, the Fungitell assay (FA) (colorimetric) and the Wako assay (WA) (turbidimetric) over a 4-month period to prospectively test 171 patients who mainly had hematological conditions (62%) and experienced episodes (n = 175) of suspected invasive fungal infection. Twenty-three episodes due to BDG-producing fungi were diagnosed (pneumocystosis, n = 12; invasive aspergillosis, n = 5; candidemia, n = 3; invasive fusariosis, n = 2; hepato-splenic candidiasis, n = 1).Both assays provided similar areas under the curves (AUC = 0.9). Using the optimized positivity thresholds (≥120 pg/ml for FA and ≥ 4 pg/ml for WA), the sensitivity and specificity were 81.8% (CI95: 61.5-92.7), 94.8% (90.1-97.3) for FA and 81.8% (61.5-92.7), 95.4% (90.9-97.8) for WA. Negative predictive value was 97.3% (93.3-99.0) for both tests. If the manufacturer's positivity threshold (≥11 pg/ml) was applied, the WA sensitivity decreased to 50%. Among 71 patients with bacterial infections, 21.1% were FA-positive and 5.6% were WA-positive (p < 10-2).The WA performed similarly as compared to the FA with an optimized cutoff value. The WA is a single sample test that is clinically relevant when a prompt therapeutic decision is required.
Serum (1→3)-β-D-glucan testing is dominated by two kits including Fungitell colorimetric assay (FA) and the Wako turbidimetric assay (WA). We compared them prospectively and observed that they both perform similarly when selecting their optimal threshold (≥120 pg/ml for FA and ≥ 4 pg/ml for WA).
血清(1→3)-β-D-葡聚糖(BDG)是一种真菌的通用抗原,在一些侵袭性真菌感染(IFI)中被检测到。我们在 4 个月的时间里比较了两种商业试剂盒,Fungitell 检测法(FA)(比色法)和 Wako 检测法(WA)(比浊法),前瞻性地检测了 171 名主要患有血液系统疾病(62%)和经历了 175 次疑似侵袭性真菌感染发作的患者。诊断出 23 例由产 BDG 的真菌引起的感染(卡氏肺孢子虫病,n=12;侵袭性曲霉病,n=5;念珠菌血症,n=3;侵袭性镰刀菌病,n=2;肝脾念珠菌病,n=1)。两种检测方法的曲线下面积(AUC)相似(AUC=0.9)。使用优化的阳性阈值(FA 为≥120 pg/ml,WA 为≥4 pg/ml),FA 的灵敏度和特异性分别为 81.8%(95%CI95:61.5-92.7)和 94.8%(90.1-97.3),WA 分别为 81.8%(61.5-92.7)和 95.4%(90.9-97.8)。两种检测方法的阴性预测值均为 97.3%(93.3-99.0)。如果应用制造商的阳性阈值(≥11 pg/ml),则 WA 的灵敏度降至 50%。在 71 名患有细菌感染的患者中,21.1%的患者 FA 阳性,5.6%的患者 WA 阳性(p<10-2)。WA 的表现与优化截断值的 FA 相似。当需要快速治疗决策时,WA 是一种单次样本检测,在临床上具有相关性。
血清(1→3)-β-D-葡聚糖检测主要由两种试剂盒组成,包括 Fungitell 比色法(FA)和 Wako 比浊法(WA)。我们前瞻性地比较了它们,观察到当选择最佳阈值(FA 为≥120 pg/ml,WA 为≥4 pg/ml)时,它们的性能相似。