Performance of the beta-glucan test for the diagnosis of invasive fusariosis and scedosporiosis: a meta-analysis

Author:

Lamoth Frederic12ORCID,Nucci Marcio34ORCID,Fernandez-Cruz Ana5ORCID,Azoulay Elie6,Lanternier Fanny78,Bremerich Jens9,Einsele Hermann10,Johnson Elizabeth11,Lehrnbecher Thomas12,Mercier Toine1314,Porto Luciana15,Verweij Paul E16ORCID,White Lewis17ORCID,Maertens Johan14,Alanio Alexandre718ORCID,Aerts Robina,Akova Murat,Alanio Alexandre,Averbuch Diana,Blennow Ola,Bretagne Stéphane,Busca Alessandro,Calandra Thierry,Cesaro Simone,Cordonnier Catherine,De La Camara Rafael,Garcia-Vidal Caroline,Gil Lidia,Groll Andreas,Herbrecht Raoul,Hirsch Hans,Hubacek Peter,Indolfi Giuseppe,Kassa Csaba,Lagrou Katrien,Lamoth Frederic,Lehrnbecher Thomas,Ljungman Per,Maertens Johan,Mallet Vincent,Martino Rodrigo,Mehra Varun,Mercier Toine,Mikulska Malgorzata,Nucci Marcio,Pagano Livio,Perruccio Katia,PiÑana Jose Luis,Porto Luciana,Robin Christine,Roilides Emmanuel,Slavin Monica,Styczynski Jan,Tverdek Frank,Verweij Paul,Vissing Nadja Hawwa,White Lewis,Xhaard Alienor,Spychala Olga Zajac,

Affiliation:

1. Infectious Diseases Service, Department of Medicine, Lausanne University Hospital and University of Lausanne , Lausanne , Switzerland

2. Institute of Microbiology, Department of Laboratory Medicine and Pathology, Lausanne University Hospital and University of Lausanne , Lausanne , Switzerland

3. University Hospital, Federal University of Rio de Janeiro , Rio de Janeiro, Brazil

4. Grupo Oncoclinicas , Brazil

5. Infectious Disease Unit, Internal Medicine Department, Puerta de Hierro-Majadahonda University Hospital, Fundación de Investigación Puerta de Hierro-Segovia de Arana, Universidad Autónoma de Madrid , Madrid, Spain

6. Médecine Intensive et Réanimation, APHP, Hôpital Saint-Louis, Paris Cité University , Paris, France

7. Institut Pasteur, Centre National de Référence Mycoses Invasives et Antifongiques, Groupe de recherche Mycologie Translationnelle, Département de Mycologie , Université Paris Cité, Paris, France

8. Infectious Diseases Unit, Hopital Necker Enfants malades, APHP, Necker-Pasteur Center for Infectious Diseases and Tropical Medicine , Paris , France

9. Cardiothoracic Imaging Section, Department of Radiology, Basel University Hospital , 4031 Basel , Switzerland

10. University Hospital Würzburg , Internal Medicine II, Würzburg, Germany

11. UK Health Security Agency (UKHSA) Mycology Reference Laboratory, Southmead Hospital , Bristol , UK and MRC Centre for Medical Mycology, Exeter University, Exeter , UK

12. Division of Pediatric Hematology and Oncology, Hospital for Children and Adolescents, University Hospital, Johann Wolfgang Goethe University , Frankfurt am Main, Germany

13. Department of Oncology-Hematology , AZ Sint-Maarten, Mechelen , Belgium

14. Department of Microbiology, Immunology, and Transplantation, KU Leuven , Leuven , Belgium and Department of Hematology, University Hospitals Leuven, Leuven , Belgium

15. Division of Neuroradiology, Pediatric Neuroradiology Department, University Hospital, Johann Wolfgang Goethe University , Frankfurt am Main, Germany

16. Department of Medical Microbiology, Radboud University Center , Nijmegen , The Netherlands

17. Public Health Wales Mycology Reference Laboratory and Cardiff University Centre for Trials Research/Division of Infection and Immunity , UHW, Cardiff , UK

18. Parasitology-Mycology laboratory Department , AP-HP, Hôpital Saint-Louis, Paris , France

Abstract

AbstractThe (1→3)-β-D-glucan (BDG) is a component of the fungal cell wall that can be detected in serum and used as an adjunctive tool for the diagnosis of invasive mold infections (IMI) in patients with hematologic cancer or other immunosuppressive conditions. However, its use is limited by modest sensitivity/specificity, inability to differentiate between fungal pathogens, and lack of detection of mucormycosis. Data about BDG performance for other relevant IMI, such as invasive fusariosis (IF) and invasive scedosporiosis/lomentosporiosis (IS) are scarce.The objective of this study was to assess the sensitivity of BDG for the diagnosis of IF and IS through systematic literature review and meta-analysis. Immunosuppressed patients diagnosed with proven or probable IF and IS, with interpretable BDG data were eligible. A total of 73 IF and 27 IS cases were included. The sensitivity of BDG for IF and IS diagnosis was 76.7% and 81.5%, respectively. In comparison, the sensitivity of serum galactomannan for IF was 27%. Importantly, BDG positivity preceded the diagnosis by conventional methods (culture or histopathology) in 73% and 94% of IF and IS cases, respectively. Specificity was not assessed because of lacking data. In conclusion, BDG testing may be useful in patients with suspected IF or IS. Combining BDG and galactomannan testing may also help differentiating between the different types of IMI.

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,General Medicine

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