Diagnostic Value of Serum Biomarkers for Invasive Aspergillosis in Haematologic Patients.

Galactomannan Ag Platelia MycoGENIE PCR Wako Beta-D-Glucan biomarkers galactomannan Ag VirClia haematologic patients invasive aspergillosis

Journal

Journal of fungi (Basel, Switzerland)
ISSN: 2309-608X
Titre abrégé: J Fungi (Basel)
Pays: Switzerland
ID NLM: 101671827

Informations de publication

Date de publication:
20 Sep 2024
Historique:
received: 13 08 2024
revised: 17 09 2024
accepted: 18 09 2024
medline: 27 9 2024
pubmed: 27 9 2024
entrez: 27 9 2024
Statut: epublish

Résumé

Invasive aspergillosis (IA) is a significant cause of morbidity and mortality in patients with haematological malignancies. Accurate diagnosis of IA is challenging due to non-specific symptoms and the impact of antifungal prophylaxis on biomarker sensitivity. This retrospective study evaluated the diagnostic performance of three serum biomarkers: Most patients diagnosed with proven or probable IA were acute myeloid leukaemia or myelodysplastic syndrome patients receiving mould-active antifungal prophylaxis or treatment (71%). VirClia demonstrated high sensitivity (100%) for detecting IA, with a specificity of 83%. Wako BDG and MycoGENIE PCR showed lower sensitivities for IA (57% and 64%, respectively). MycoGENIE PCR detected Accurate diagnosis of IA remains challenging, especially in patients who have received mould-active antifungal treatment. VirClia showed comparable performance to Platelia, suggesting its potential for routine use. However, Wako BDG and MycoGENIE PCR results were less favourable in our study cohort. Nevertheless, MycoGENIE PCR detected two probable co-infections with

Sections du résumé

BACKGROUND BACKGROUND
Invasive aspergillosis (IA) is a significant cause of morbidity and mortality in patients with haematological malignancies. Accurate diagnosis of IA is challenging due to non-specific symptoms and the impact of antifungal prophylaxis on biomarker sensitivity.
METHODS METHODS
This retrospective study evaluated the diagnostic performance of three serum biomarkers:
RESULTS RESULTS
Most patients diagnosed with proven or probable IA were acute myeloid leukaemia or myelodysplastic syndrome patients receiving mould-active antifungal prophylaxis or treatment (71%). VirClia demonstrated high sensitivity (100%) for detecting IA, with a specificity of 83%. Wako BDG and MycoGENIE PCR showed lower sensitivities for IA (57% and 64%, respectively). MycoGENIE PCR detected
CONCLUSIONS CONCLUSIONS
Accurate diagnosis of IA remains challenging, especially in patients who have received mould-active antifungal treatment. VirClia showed comparable performance to Platelia, suggesting its potential for routine use. However, Wako BDG and MycoGENIE PCR results were less favourable in our study cohort. Nevertheless, MycoGENIE PCR detected two probable co-infections with

Identifiants

pubmed: 39330420
pii: jof10090661
doi: 10.3390/jof10090661
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : FONDATION MONT-GODINNE
ID : FMG-BR-2023-008

Auteurs

Isabel Montesinos (I)

Laboratory Medicine-Microbiology, Centre Hospitalier Universitaire (CHU) Université Catholique de Louvain (UCL) Namur Site Godinne, 5530 Yvoir, Belgium.

Imane Saad Albichr (IS)

Laboratory Medicine-Microbiology, Centre Hospitalier Universitaire (CHU) Université Catholique de Louvain (UCL) Namur Site Godinne, 5530 Yvoir, Belgium.

Elodie Collinge (E)

Haematological Department, Centre Hospitalier Universitaire (CHU) Université Catholique de Louvain (UCL) Namur Site Godinne, 5530 Yvoir, Belgium.

Bénédicte Delaere (B)

Infectiology Department, Centre Hospitalier Universitaire (CHU) Université Catholique de Louvain (UCL) Namur Site Godinne, 5530 Yvoir, Belgium.

Te-Din Huang (TD)

Laboratory Medicine-Microbiology, Centre Hospitalier Universitaire (CHU) Université Catholique de Louvain (UCL) Namur Site Godinne, 5530 Yvoir, Belgium.

Pierre Bogaerts (P)

Laboratory Medicine-Microbiology, Centre Hospitalier Universitaire (CHU) Université Catholique de Louvain (UCL) Namur Site Godinne, 5530 Yvoir, Belgium.

Corentin Deckers (C)

Laboratory Medicine-Microbiology, Centre Hospitalier Universitaire (CHU) Université Catholique de Louvain (UCL) Namur Site Godinne, 5530 Yvoir, Belgium.

Mai Hamouda (M)

Pharmacy Faculty, Namur University, 5000 Namur, Belgium.

Patrick M Honoré (PM)

Intensive Care Unit, Centre Hospitalier Universitaire (CHU) Université Catholique de Louvain (UCL) Namur Site Godinne, 5530 Yvoir, Belgium.

Pierre Bulpa (P)

Intensive Care Unit, Centre Hospitalier Universitaire (CHU) Université Catholique de Louvain (UCL) Namur Site Godinne, 5530 Yvoir, Belgium.

Anne Sonet (A)

Haematological Department, Centre Hospitalier Universitaire (CHU) Université Catholique de Louvain (UCL) Namur Site Godinne, 5530 Yvoir, Belgium.

Classifications MeSH