(1-3)-Beta-D-glucan in association with lactate dehydrogenase as biomarkers of Pneumocystis pneumonia (PcP) in HIV-infected patients

被引:51
作者
Esteves, F. [1 ]
Lee, C. -H. [2 ]
de Sousa, B. [3 ]
Badura, R. [4 ]
Seringa, M. [1 ]
Fernandes, C. [1 ]
Gaspar, J. F. [5 ]
Antunes, F. [4 ]
Matos, O. [1 ,6 ]
机构
[1] Univ Nova Lisboa, Unidade Parasitol Med, Grp Protozoarios Oportunistas VIH & Outros Protoz, CMDT Inst Higiene & Med Trop, P-1349008 Lisbon, Portugal
[2] Indiana Univ Sch Med, Dept Pathol & Lab Med, Indianapolis, IN 46202 USA
[3] Univ Coimbra, CMDT, Fac Psicol & Ciencias Educ, Coimbra, Portugal
[4] FM UL, Ctr Hosp Lisboa Norte, Hosp Santa Maria, Lisbon, Portugal
[5] Univ Nova Lisboa, Dept Genet, CIGMH, Fac Ciencias Med, P-1349008 Lisbon, Portugal
[6] Univ Nova Lisboa, Unidade Protozoarios Oportunistas VIH & Outras Pr, Inst Higiene & Med Trop, P-1349008 Lisbon, Portugal
关键词
BETA-D-GLUCAN; BRONCHOALVEOLAR LAVAGE SPECIMENS; CARINII-PNEUMONIA; JIROVECII PNEUMONIA; CLINICAL UTILITY; SERUM; DIAGNOSIS; ASSAY; COLONIZATION; INDICATOR;
D O I
10.1007/s10096-014-2054-6
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Pneumocystis pneumonia (PcP) is a major HIV-related illness caused by Pneumocystis jirovecii. Definitive diagnosis of PcP requires microscopic detection of P. jirovecii in pulmonary specimens. The objective of this study was to evaluate the usefulness of two serum markers in the diagnosis of PcP. Serum levels of (1-3)-beta-d-glucan (BG) and lactate dehydrogenase (LDH) were investigated in 100 HIV-positive adult patients and 50 healthy blood donors. PcP cases were confirmed using indirect immunofluorescence with monoclonal anti-Pneumocystis antibodies and nested-PCR to amplify the large subunit mitochondrial rRNA gene of P. jirovecii in pulmonary specimens. BG and LDH levels in serum were measured using quantitative microplate-based assays. BG and LDH positive sera were statistically associated with PcP cases (P a parts per thousand currency signaEuro parts per thousand 0.001). Sensitivity, specificity, positive/negative predictive values (PPV/NPV), and positive/negative likelihood ratios (PLR/NLR) were 91.3 %, 61.3 %, 85.1 %, 79.2 %, 2.359, and 0.142, respectively, for the BG kit assay, and 91.3 %, 35.5 %, 75.9 %, 64.7 %, 1.415 and 0.245, respectively, for the LDH test. Serologic markers levels combined with the clinical diagnostic criteria for PcP were evaluated for their usefulness in diagnosis of PcP. The most promising cutoff levels for diagnosis of PcP were determined to be 400 pg/ml of BG and 350 U/l of LDH, which combined with clinical data presented 92.8 % sensitivity, 83.9 % specificity, 92.8 % PPV, 83.9 % NPV, 5.764 PLR and 0.086 NLR (P < 0.001). This study confirmed that BG is a reliable indicator for detecting P. jirovecii infection. The combination between BG/LDH levels and clinical data is a promising alternative approach for PcP diagnosis.
引用
收藏
页码:1173 / 1180
页数:8
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