Diagnostic value of serum human Galactomannan aspergillus antigen and 1,3‐beta‐D‐glucan in immunocompromised patient suspected fungal infection
Autor: | Hani Susianti, Ungky Agus Setyawan, Lydiana Parmadi, Novi Khila Firani, Teguh Rahayu Sartono |
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Rok vydání: | 2021 |
Předmět: |
Male
0301 basic medicine beta-Glucans Microbiological culture Lymphocyte Clinical Biochemistry Serology Mannans chemistry.chemical_compound 0302 clinical medicine Immunology and Allergy Medicine Research Articles Hematology biology Middle Aged Prognosis immunocompromised Medical Laboratory Technology fungal Infection Aspergillus 1 3-Beta-glucan synthase medicine.anatomical_structure 030220 oncology & carcinogenesis Female Research Article Adult Microbiology (medical) medicine.medical_specialty Antigens Fungal Adolescent Neutropenia Immunocompromised Host Young Adult 03 medical and health sciences Galactomannan Internal medicine Humans haematology parameters Aged business.industry Monocyte Biochemistry (medical) Public Health Environmental and Occupational Health Galactose medicine.disease Cross-Sectional Studies 030104 developmental biology Mycoses chemistry galactomannan Immunology biology.protein 1 3‐beta‐d‐glucan business Follow-Up Studies |
Zdroj: | Journal of Clinical Laboratory Analysis |
ISSN: | 1098-2825 0887-8013 |
DOI: | 10.1002/jcla.23806 |
Popis: | Background The prevalence of fungal infection (FI) in developing countries is high, but the diagnosis of FI is still challenging to determine, so it is needed evaluation of biomarkers other than microbiological culture, because the culture has low sensitivity, high cost, not available in every laboratory and needs a long time. The detection of human galactomannan Aspergillus antigen (GAL) and 1,3‐beta‐D‐glucan (BDG) on the fungal cell wall could be the promising biomarkers for fungal infection. Neutropenia, lymphopenia and CD4T cells in the immunocompromised patients are essential factors, but these cell associations with BDG and GAL levels have not been evaluated yet. The study aimed to evaluate GAL and BDG for detecting fungal infection and their association with total leucocyte count, neutrophil, monocyte, lymphocyte and CD4T cells. Method A cross‐sectional study was conducted among 86 patient with suspected FI. Fungal infection established using EORTC/MSG criteria. Serology test performed using ELISA. Leucocyte cells were measured using a haematology autoanalyser, and CD4T cells were analysed using BD FACSPresto. Statistical analysis obtained using Spearman's correlation coefficient, ROC curve analysis and 2 × 2 contingency table. Results Serum Galactomannan and BDG had a significant correlation with CD4T cells and total lymphocyte count (p 0.3 had sensitivity 54.6%, specificity 87.5% and AUC 0.71; meanwhile, the BDG cut‐off >115.78 pg/ mL had sensitivity 71.2%, specificity 52.4% and AUC 0.63 for detecting fungal infection. Conclusions The immunocompromised patients can undergo GAL for determining the diagnose of FI. The lower the CD4T cells and total lymphocyte count, the higher the GAL and BDG serum levels. The prevalence of fungal infection (FI) in developing countries is high, but the diagnosis of FI is still challenging to determine, so it is needed evaluation of biomarkers other than microbiological culture, because the culture has low sensitivity, high cost, not available in every laboratory and needs a long time. The detection of Human Galactomannan Aspergillus Antigen (GAL) and 1,3‐Beta‐D‐Glucan (BDG) on the fungal cell wall could be the promising biomarkers for fungal infection. Neutropenia, lymphopenia and CD4T‐cells in the immunocompromised patients are essential factors, but these cells association with BDG and GAL levels have not evaluated yet. The study aimed to evaluate GAL and BDG for detecting fungal infection and their association with total leucocyte count, neutrophil, monocyte, lymphocyte and CD4T‐cells. As the results of this study, GAL and BDG had a significant correlation with CD4T‐cells and total lymphocyte count (p 0.3 had sensitivity 54.6%, specificity 87.5% and AUC 0.71, meanwhile the BDG cut off >115.78 pg/ mL had sensitivity 71.2%, specificity 52.4% and AUC 0.63 for detecting fungal infection. So that for conclusions, immunocompromised patients can undergo GAL for determining the diagnose of FI. The lower the CD4T‐cells and total lymphocyte count, the higher the GAL and BDG serum concentration. |
Databáze: | OpenAIRE |
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