MycoBiomDB – Record Details (MyCo_1568)

Biomarker Record Details

Database ID: MyCo_1568
DB IDMyCo_1568
TitleEarly proinflammatory cytokines and C‐reactive protein trends as predictors of outcome in invasive Aspergillosis
Year2010
PMID20879853
Fungal Diseases involvedInvasive aspergillosis
Associated Medical ConditionNone
GenusAspergillus
Speciesspp.
OrganismAspergillus spp.
Ethical StatementThis study was approved by the Eu-ropean Organization for Research and Treatment of Cancer.
Site of InfectionNone
Opportunistic invasiveInvasive
Sample typeBody fluid
Sample sourceSerum
Host GroupHuman
Host Common nameHuman
Host Scientific nameHomo sapiens
Biomarker NameCRP
Biomarker Full NameC-reactive protein
Biomarker TypeDiagnostic
BiomoleculeProtein
Geographical LocationUSA
CohortStudy patients were from the Global Comparative Aspergillosis Study (protocol 150–307), a multicenter randomized trial that compared the efficacy of vor- iconazole versus amphotericin B in the primary treatment of invasive aspergillosis. A total of 539 serum specimens serially collected from 119 patients enrolled in the clinical trial were available for analysis.
Cohort No.119
Age GroupNone
P ValueNone
SensitivityNone
SpecificityNone
Positive Predictive ValueNone
MICNone
Fold ChangeNone
PathwayNone
Disease Introduction MechanismInvasive aspergillosis continues to be a leading cause of mortality and morbidity among patients treated for he- matological malignancies. The adverse outcomes associated with acquisition of the disease may in part be attributable to the compromised immune system of at-risk patients. Securing a firm diagnosis of invasive aspergillosis remains difficult. Management of invasive aspergillosis is complicated by the absence of appro-priate tools with which to assess progress and treatment response.
TechniqueELISA
Analysis MethodELISA Based
ELISA kitssandwich enzyme-linked immunosorbent assay (ELISA) kits (Pelikine Compact; CLB)
Assay DataNone
Validation Techniques usedELISA
Up Regulation Down RegulationIncrease
Sequence DataNone
External LinkNone