Abstract

The early diagnosis of invasive aspergillosis (IA) relies mainly on computed tomography imaging and testing for fungal biomarkers such as galactomannan (GM). We compared an established ELISA for the detection of GM with a turbidimetric assay for detection of the panfungal biomarker β-D-glucan (BDG) for early diagnosis of IA. A total of 226 serum specimens from 47 proven and seven probable IA cases were analysed. Sensitivity was calculated for samples obtained closest to the day of IA-diagnosis (d0). Additional analyses were performed by including samples obtained during the presumed course of disease. Most IA cases involved the respiratory system (63%), and Aspergillus fumigatus was the most frequently isolated species (59%). For proven cases, sensitivity of BDG/GM analysis was 57%/40%. Including all samples dating from –6 to +1 weeks from d0 increased sensitivities to 74%/51%. Sensitivity of BDG testing was as high as or higher than GM testing for all subgroups and time intervals analysed. BDG testing was less specific (90–93%) than GM testing (99–100%). Combining BDG and GM testing resulted in sensitivity/specificity of 70%/91%. Often, BDG testing was positive before GM testing. Our study backs the use of BDG for diagnosis of suspected IA. We suggest combining BDG and GM to improve the overall sensitivity.

Highlights

  • Invasive aspergillosis (IA) is a life-threatening and underdiagnosed fungal infection that is caused by moulds of the genus Aspergillus [1]

  • We retrospectively identified 47 and seven episodes of proven and probable invasive aspergillosis (IA) according to the EORTC/MSG criteria, which occurred in the period of 2009–2018 (Tables 1–3) [13]

  • Forty-seven (87%) patients with proven and seven (13%) episodes of probable IA according to the revised definitions of the EORTC/MSG consensus group were included in this study [13]

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Summary

Introduction

Invasive aspergillosis (IA) is a life-threatening and underdiagnosed fungal infection that is caused by moulds of the genus Aspergillus [1]. The most important risk factor for IA is impaired host defence. Patients undergoing myeloablative therapies and hematopoietic stem cell transplantation (HSCT) are at highest risk [2,3]. J. Fungi 2020, 6, 253; doi:10.3390/jof6040253 www.mdpi.com/journal/jof. J. Fungi 2020, 6, 253 been identified, such as systemic steroid therapy, intensive care unit admission, and influenza [4,5,6,7]

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