MycoBiomDB – Record Details (MyCo_6051)

Biomarker Record Details

Database ID: MyCo_6051
DB IDMyCo_6051
TitleLevels of interleukin (IL)-6 and IL-8 are elevated in serum and bronchoalveolar lavage fluid of haematological patients with invasive pulmonary aspergillosis
Year2017
PMID28877383
Fungal Diseases involvedInvasive pulmonary aspergillosis
Associated Medical ConditionNone
GenusAspergillus
Speciesspp.
OrganismAspergillus spp.
Ethical StatementThe study protocol was approved by the local ethics committees, Medical University Graz, Austria (EC-numbers 25-
Site of InfectionNone
Opportunistic invasiveNone
Sample typeBody fluid
Sample sourceSerum
Host GroupHuman
Host Common nameHuman
Host Scientific nameHomo sapiens
Biomarker NameIL-6
Biomarker Full NameInterleukin-6
Biomarker TypeDiagnostic
BiomoleculeProtein
Geographical LocationAustria
CohortThis nested case-¬ control study of prospectively collected data com- prised paired routine serum and BALF samples obtained on the same day from 10 cases with IPA and 20 matched controls without IPA.
Cohort No.10 Patients and 20 control
Age Group26-73
P Valuep=.011
SensitivityNone
SpecificityNone
Positive Predictive ValueNone
MICNone
Fold ChangeNone
PathwayNone
Disease Introduction MechanismInvasive pulmonary aspergillosis (IPA) is associated with high morbidity and mortality among patients with underlying haematological malignancies. Due to the crude mortality of 80%-¬ 90% in the absence of adequate treatment, timely diagnosis and early start of antifungal therapy are key factors in the successful treatment of IPA. The introduction of non-¬ cultural diagnostic tests for IPA in blood and bronchoalveolar lavage fluid (BALF), including galactomannan antigen (GM) testing, PCR, the Aspergillus specific lateral flow device test and 1,3-¬ β- d- glucan (BDG) testing, was associated with a significant increase in the rate of IPA-¬ diagnosed premortem (vs postmortem). Despite these significant advancements, performance of these non-cultural diagnostic tests is varying, and the search for a reliable gold standard for diagnosis of IPA premortem continues.
TechniqueImmunological assay
Analysis MethodProcartaPlex® 11plex immunoassay
ELISA kitsNone
Assay DataNone
Validation Techniques usedProcartaPlex® 11plex immunoassay
Up Regulation Down RegulationPositive
Sequence DataNone
External LinkNone