Evidence map›Paper›PMID 27419189›Full record

ArticleOpen forum infectious diseases2016

Prospective Evaluation of Serum β-Glucan Testing in Patients With Probable or Proven Fungal Diseases.

Cécile Angebault, Fanny Lanternier, Frédéric Dalle, Cécile Schrimpf, Anne-Laure Roupie, Aurélie Dupuis, Aurélie Agathine, Anne Scemla, Etienne Paubelle, Denis Caillot and 6 more

Abstract read
In one paragraph

Article in Open forum infectious diseases, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 2 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

31 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Review
  5. Observational
  6. Article
  7. Review
  8. The Diagnostic Sensitivity of Beta-D-Glucan Assay in Patients with Chronic Disseminated Candidiasis.Mediterranean journal of hematology and infectious diseases · 2025
    Article
  9. Article
  10. Article
  11. Review
  12. Observational
  13. Multicenter Prospective Study of Biomarkers for Diagnosis of Invasive Candidiasis in Children and Adolescents.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2022
    Observational
  14. Article
  15. Review
  16. Beta-D-Glucan in Patients with Haematological Malignancies.Journal of fungi (Basel, Switzerland) · 2021
    Review
  17. Article
  18. DisseminatedClinical case reports · 2021
    Article
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Cécile AngebaultUnitéde Parasitologie-Mycologie, Service de Microbiologie Clinique; Université Paris Descartes, Sorbonne Paris-Cité.
Fanny LanternierCentre d'Infectiologie Necker Pasteur; Université Paris Descartes, Sorbonne Paris-Cité,; Unité de Mycologie Médicale, Centre National de Référence Mycoses Invasives et Antifongiques, Institut Pasteur, Paris.
Frédéric DalleService de Parasitologie-Mycologie.
Cécile SchrimpfCentre d'Infectiologie Necker Pasteur.
Anne-Laure RoupieCentre d'Infectiologie Necker Pasteur.
Aurélie DupuisUnité de Parasitologie-Mycologie, Service de Microbiologie Clinique.
Aurélie AgathineUnité de Parasitologie-Mycologie, Service de Microbiologie Clinique.
Anne ScemlaService de Néphrologie et Transplantation Adulte; Université Paris Descartes, Sorbonne Paris-Cité,; Réseau Thématique de Recherche et de SoinsCentaure, Labex Transplantex, Paris.
Etienne PaubelleService d'Hématologie Adulte; Université Paris Descartes, Sorbonne Paris-Cité.
Denis CaillotService d'Hématologie Clinique , Centre Hospitalier Universitaire Dijon Bourgogne .
Bénédicte NevenUnité d'Immunologie, Hématologie et Rhumatologie Pédiatriques.
Pierre FrangeUnité d'Immunologie, Hématologie et Rhumatologie Pédiatriques; Unité d'Hygiène, Service de Microbiologie Clinique, Hôpital Necker-Enfants malades, Assistance Publique des Hôpitaux de Paris.
Felipe SuarezService d'Hématologie Adulte; Université Paris Descartes, Sorbonne Paris-Cité.
Christophe d'EnfertUnité Biologie et Pathogénicité Fongiques, Département de Mycologie, Institut Pasteur, Paris; Institut National de la Recherche Agronomique, Unité Sous Contrat 2019, Paris, France.
Olivier LortholaryCentre d'Infectiologie Necker Pasteur; Université Paris Descartes, Sorbonne Paris-Cité,; Unité de Mycologie Médicale, Centre National de Référence Mycoses Invasives et Antifongiques, Institut Pasteur, Paris.
Marie-Elisabeth BougnouxUnitéde Parasitologie-Mycologie, Service de Microbiologie Clinique; Université Paris Descartes, Sorbonne Paris-Cité,; Unité Biologie et Pathogénicité Fongiques, Département de Mycologie, Institut Pasteur, Paris; Institut National de la Recherche Agronomique, Unité Sous Contrat 2019, Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background.  Early diagnosis and treatment are crucial in invasive fungal diseases (IFD). Serum (1-3)-β-d-glucan (BG) is believed to be an early IFD marker, but its diagnostic performance has been ambiguous, with insufficient data regarding sensitivity at the time of IFD diagnosis (TOD) and according to outcome. Whether its clinical utility is equivalent for all types of IFD remains unknown. Methods.  We included 143 patients with proven or probable IFD (49 invasive candidiasis, 45 invasive aspergillosis [IA], and 49 rare IFD) and analyzed serum BG (Fungitell) at TOD and during treatment. Results.  (1-3)-β-d-glucan was undetectable at TOD in 36% and 48% of patients with candidemia and IA, respectively; there was no correlation between negative BG results at TOD and patients' characteristics, localization of infection, or prior antifungal use. Nevertheless, patients with candidemia due to Candida albicans were more likely to test positive for BG at TOD (odds ratio = 25.4, P = .01) than patients infected with other Candida species. In 70% of the patients with a follow-up, BG negativation occurred in >1 month for candidemia and >3 months for IA. A slower BG decrease in patients with candidemia was associated with deep-seated localizations (P = .04). Thirty-nine percent of patients with rare IFD had undetectable BG at TOD; nonetheless, all patients with chronic subcutaneous IFD tested positive at TOD. Conclusions.  Undetectable serum BG does not rule out an early IFD, when the clinical suspicion is high. After IFD diagnostic, kinetics of serum BG are difficult to relate to clinical outcome.

Indexed as

(1-3)-β-d-glucandiagnostic toolinvasive fungal diseaseskinetics

Identifiers

PMID27419189
PMCPMC4942764

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.