Comparison of galactomannan, beta-D-glucan, and Aspergillus DNA in sera of high-risk adult patients with hematological malignancies for the diagnosis of invasive aspergillosis

被引:10
作者
Boluk, Gulcin [1 ]
Kazak, Esra [1 ]
Ozkalemkas, Fahir [2 ]
Ener, Beyza [3 ]
Akalin, Halis [1 ]
Agca, Harun [3 ]
Okuturlar, Yildiz [4 ]
Keskin, Kursad [5 ]
Burgazlioglu, Basak [6 ]
Ali, Ridvan [2 ]
机构
[1] Uludag Univ, Dept Infect Dis & Clin Microbiol, Fac Med, Bursa, Turkey
[2] Uludag Univ, Dept Internal Med, Hematol Unit, Fac Med, Bursa, Turkey
[3] Uludag Univ, Dept Med Microbiol, Fac Med, Bursa, Turkey
[4] Bakirkoy Dr Sadi Konuk Training & Res Hosp, Dept Internal Med, Istanbul, Turkey
[5] Medicabil Hosp, Dept Internal Med, Bursa, Turkey
[6] Rentip Hosp, Dept Chest Dis, Bursa, Turkey
关键词
Invasive aspergillosis; galactomannan test; beta-D-glucan test; specific DNA; LINKED-IMMUNOSORBENT-ASSAY; REAL-TIME PCR; POLYMERASE-CHAIN-REACTION; CELL TRANSPLANT RECIPIENTS; FUNGAL-INFECTIONS; CIRCULATING GALACTOMANNAN; PULMONARY ASPERGILLOSIS; BRONCHOALVEOLAR LAVAGE; CLINICAL-EVALUATION; ANTIGEN-DETECTION;
D O I
10.3906/sag-1408-100
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Bckground/aim: Invasive aspergillosis (IA) is a fatal infection that is difficult to diagnose in immunocompromised patients. In this study, Aspergillus-specific DNA was searched using real-time PCR (RT-PCR) in serum samples. Galactomannan (GM) and/or beta-D-glucan (BDG) tests were previously performed on these samples for 70 neutropenic patients with hematological malignancy. Materials and methods: The patients were categorized according to the criteria of the European Organization for Research and Treatment of Cancer/Mycoses Study Group (EORTC/MSG). Among the patient serum samples, the first positive GM or BDG test sample and the median sample of GM or BDG test for negative patients were used to detect DNA levels by RT-PCR method (Light Cycler 480, Roche Molecular Biochemicals, Meylan, France) using a commercial kit (Way2Gene Fungi; Genmar, Izmir, Turkey). Results: When the proven and probable IA group were considered as real patients, sensitivity of Aspergillus-specific DNA test was 90%, specificity was 73.3%, positive predictive value was 81.8%, and negative predictive value was 84.6%. Conclusion: This study found that searching for specific DNA by RT-PCR method has a sensitivity as high as the GM test. Although specificity was rather low, it was concluded that it can be used jointly with GM and BDG tests after decreasing contamination by severe laboratory applications.
引用
收藏
页码:335 / 342
页数:8
相关论文
共 48 条
[1]   Potential of polymerase chain reaction and galactomannan for the diagnosis of invasive aspergillosis in patients with febrile neutropenia [J].
Aslan, Muge ;
Oz, Yasemin ;
Aksit, Filiz ;
Akay, Olga M. .
MYCOSES, 2015, 58 (06) :343-349
[2]  
Aydogan S, 2010, MIKROBIYOL BUL, V44, P441
[3]   Laboratory diagnostics of invasive fungal infections: an overview with emphasis on molecular approach [J].
Baskova, Lenka ;
Buchta, Vladimir .
FOLIA MICROBIOLOGICA, 2012, 57 (05) :421-430
[4]   Quantitative galactomannan detection is superior to PCR in diagnosing and monitoring invasive pulmonary aspergillosis in an experimental rat model [J].
Becker, MJ ;
de Marie, S ;
Willemse, D ;
Verbrugh, HA ;
Bakker-Woudenberg, IAJM .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (04) :1434-1438
[5]   Comparison of serum galactomannan antigen detection and competitive polymerase chain reaction for diagnosing invasive aspergillosis [J].
Bretagne, S ;
Costa, JM ;
Bart-Delabesse, E ;
Dhédin, N ;
Rieux, C ;
Cordonnier, C .
CLINICAL INFECTIOUS DISEASES, 1998, 26 (06) :1407-1412
[6]   Prospective clinical evaluation of a LightCycler™-mediated polymerase chain reaction assay, a nested-PCR assay and a galactomannan enzyme-linked immunosorbent assay for detection of invasive aspergillosis in neutropenic cancer patients and haematological stem cell transplant recipients [J].
Buchheidt, D ;
Hummel, M ;
Schleiermacher, D ;
Spiess, B ;
Schwerdtfeger, R ;
Cornely, OA ;
Wilhelm, S ;
Reuter, S ;
Kern, W ;
Südhoff, T ;
Mörz, H ;
Hehlmann, R .
BRITISH JOURNAL OF HAEMATOLOGY, 2004, 125 (02) :196-202
[7]   Real-time PCR coupled with automated DNA extraction and detection of galactomannan antigen in serum by enzyme-linked immunosorbent assay for diagnosis of invasive aspergillosis [J].
Costa, C ;
Costa, JM ;
Desterke, C ;
Botterel, F ;
Cordonnier, C ;
Bretagne, S .
JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (06) :2224-2227
[8]   Revised definitions of invasive fungal disease from the European Organization for Research and Treatment of Cancer/Invasive Fungal Infections Cooperative Group and the National Institute of Allergy and Infectious Diseases Mycoses Study Group (EORTC/MSG) Consensus Group [J].
De Pauw, Ben ;
Walsh, Thomas J. ;
Donnelly, J. Peter ;
Stevens, David A. ;
Edwards, John E. ;
Calandra, Thierry ;
Pappas, Peter G. ;
Maertens, Johan ;
Lortholary, Olivier ;
Kauffman, Carol A. ;
Denning, David W. ;
Patterson, Thomas F. ;
Maschmeyer, Georg ;
Bille, Jacques ;
Dismukes, William E. ;
Herbrecht, Raoul ;
Hope, William W. ;
Kibbler, Christopher C. ;
Kullberg, Bart Jan ;
Marr, Kieren A. ;
Munoz, Patricia ;
Odds, Frank C. ;
Perfect, John R. ;
Restrepo, Angela ;
Ruhnke, Markus ;
Segal, Brahm H. ;
Sobel, Jack D. ;
Sorrell, Tania C. ;
Viscoli, Claudio ;
Wingard, John R. ;
Zaoutis, Theoklis ;
Bennett, John E. .
CLINICAL INFECTIOUS DISEASES, 2008, 46 (12) :1813-1821
[9]   Invasive aspergillosis [J].
Denning, DW .
CLINICAL INFECTIOUS DISEASES, 1998, 26 (04) :781-803
[10]   INVASIVE ASPERGILLOSIS - PROGRESS IN EARLY DIAGNOSIS AND TREATMENT [J].
FISHER, BD ;
ARMSTRONG, D ;
YU, B ;
GOLD, JWM .
AMERICAN JOURNAL OF MEDICINE, 1981, 71 (04) :571-577