MycoBiomDB – Record Details (MyCo_5472)

Biomarker Record Details

Database ID: MyCo_5472
DB IDMyCo_5472
TitleEvaluation of real-time PCR, galactomannan enzyme-linked immunosorbent assay (ELISA), and a novel lateral-flow device for diagnosis of invasive aspergillosis
Year2013
PMID23486712
Fungal Diseases involvedInvasive aspergillosis
Associated Medical ConditionNone
GenusAspergillus
Speciesspp.
OrganismAspergillus spp.
Ethical StatementThe study was conducted as a retrospective performance assessment not requiring ethical approval.
Site of InfectionNone
Opportunistic invasiveOpportunistic
Sample typeBody fluid
Sample sourceEDTA Blood
Host GroupHuman
Host Common nameHuman
Host Scientific nameHomo sapiens
Biomarker Name28S rRNA gene
Biomarker Full Name28S rRNA gene
Biomarker TypeDiagnostic
BiomoleculeGene
Geographical LocationUK
CohortThe study comprised 103 adult hematology patients at high risk of developing IA, including eight proven cases of IA, 14 probable cases, 22 possible cases, and 59 controls not achieving an EORTC/MSG diagnosis.
Cohort No.103
Age GroupNone
P Valuep=0.0001
Sensitivity0.818
Specificity0.864
Positive Predictive ValueNone
MICNone
Fold ChangeNone
PathwayNone
Disease Introduction MechanismInvasive aspergillosis (IA) is a serious infection in immunocompromised patients. Delays in diagnosis contribute to the high morbidity and mortality associated with this disease. The detection of circulating biomarkers (DNA or antigens) indicative of IA is an attractive strategy that allows frequent testing, increasing the opportunity for detecting early infection before overt disease develops. High assay sensitivity and negative predictive value (NPV) can exclude disease, preventing unnecessary treatment in patients who are consistently negative. The number of biomarker test options is limited.
TechniquePCR
Analysis MethodAspergillus RT-PCR
ELISA kitsPlatelia ELISA kits (Bio-Rad, United Kingdom)
Assay DataNone
Validation Techniques usedELISA, PCR, LFD
Up Regulation Down RegulationIncrease
Sequence DataNone
External LinkNone