Evidence map›Paper›PMID 29788296›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2019

Comparison of Clostridioides difficile Stool Toxin Concentrations in Adults With Symptomatic Infection and Asymptomatic Carriage Using an Ultrasensitive Quantitative Immunoassay.

Nira R Pollock, Alice Banz, Xinhua Chen, David Williams, Hua Xu, Christine A Cuddemi, Alice X Cui, Matthew Perrotta, Eaman Alhassan, Brigitte Riou and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed, 2 pooled it
8.4field-weighted citation impact, top 2% of its field
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

61 citing papers in PubMed, 2 syntheses or guidelines pooled it, 97 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Current status and future perspectives of fecal immunological markers in the differential diagnosis of Clostridioides difficile infection in children.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2026
    Review
  6. Observational
  7. Article
  8. Clostridioides difficile pathogenesis and control.Nature reviews. Microbiology · 2026
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Emerging Diagnostics inInternational journal of molecular sciences · 2024
    Review
  16. Rational Design of Live Biotherapeutic Products for the Prevention ofbioRxiv : the preprint server for biology · 2024
    Article
  17. Impact of the Reverse 2-Step Algorithm forOpen forum infectious diseases · 2024
    Article
  18. Diagnostic Guidance for C. difficile Infections.Advances in experimental medicine and biology · 2024
    Article
  19. Article
  20. Host Immune Responses toTropical medicine and infectious disease · 2023
    Review

1 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 3 countries.

Nira R PollockDivisions of Infectious Disease and Gastroenterology, Department of Medicine, Beth Israel Deaconess Medical Center, Boston.
Alice BanzbioMérieux, Marcy L'Etoile, France.
Xinhua ChenDivisions of Infectious Disease and Gastroenterology, Department of Medicine, Beth Israel Deaconess Medical Center, Boston.
David WilliamsInstitutional Centers for Clinical and Translational Research, Boston Children's Hospital, Massachusetts.
Hua XuDivisions of Infectious Disease and Gastroenterology, Department of Medicine, Beth Israel Deaconess Medical Center, Boston.
Christine A CuddemiDivisions of Infectious Disease and Gastroenterology, Department of Medicine, Beth Israel Deaconess Medical Center, Boston.
Alice X CuiDivisions of Infectious Disease and Gastroenterology, Department of Medicine, Beth Israel Deaconess Medical Center, Boston.
Matthew PerrottaDivisions of Infectious Disease and Gastroenterology, Department of Medicine, Beth Israel Deaconess Medical Center, Boston.
Eaman AlhassanDivisions of Infectious Disease and Gastroenterology, Department of Medicine, Beth Israel Deaconess Medical Center, Boston.
Brigitte RioubioMérieux, Marcy L'Etoile, France.
Aude LantzbioMérieux, Marcy L'Etoile, France.
Mark A MillerbioMérieux, Marcy L'Etoile, France.
Ciaran P KellyDivisions of Infectious Disease and Gastroenterology, Department of Medicine, Beth Israel Deaconess Medical Center, Boston.
Hadassah Medical Center · ILbioMérieux (France) · FRBoston Children's Hospital · US

Funding

Ultrasensitive C.difficile toxin measurement for diagnosis and outcome predictionR01AI116596 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI POLLOCK, NIRA · 2016 to 2020
$4.1M
NIAID NIH HHS R01 AI116596
6 · The paper itself

Abstract

Background: We used an ultrasensitive, quantitative single molecule array (Simoa) immunoassay to test whether concentrations of Clostridioides (formerly Clostridium) difficile toxins A and/or B in the stool of adult inpatients with C. difficile infection (CDI) were higher than in asymptomatic carriers of toxinogenic C. difficile. Methods: Patients enrolled as CDI-NAAT had clinically significant diarrhea and a positive nucleic acid amplification test (NAAT), per US guidelines, and received CDI treatment. Potential carriers had recently received antibiotics and did not have diarrhea; positive NAAT confirmed carriage. Baseline stool samples were tested by Simoa for toxin A and B. Results: Stool toxin concentrations in both CDI-NAAT (n = 122) and carrier-NAAT (n = 44) cohorts spanned 5 logs (0 pg/mL to >100000 pg/mL). Seventy-nine of 122 (65%) CDI-NAAT and 34 of 44 (77%) carrier-NAAT had toxin A + B concentration ≥20 pg/mL (clinical cutoff). Median toxin A, toxin B, toxin A + B, and NAAT cycle threshold (Ct) values in CDI-NAAT and carrier-NAAT cohorts were similar (toxin A, 50.6 vs 60.0 pg/mL, P = .958; toxin B, 89.5 vs 42.3 pg/mL, P = .788; toxin A + B, 197.2 vs 137.3 pg/mL, P = .766; Ct, 28.1 vs 28.6, P = .354). However, when CDI/carrier cohorts were limited to those with detectable toxin, respective medians were significantly different (A: 874.0 vs 129.7, P = .021; B: 1317.0 vs 81.7, P = .003, A + B, 4180.7 vs 349.6, P = .004; Ct, 25.8 vs 27.7, P = .015). Conclusions: Toxin concentration did not differentiate an individual with CDI from one with asymptomatic carriage. Median stool toxin concentrations in groups with CDI vs carriage differed, but only when groups were defined by detectable stool toxin (vs positive NAAT).

Indexed as

AdolescentAdultAgedAged, 80 and overBacterial ProteinsBacterial ToxinsCarrier StateClostridioides difficileClostridium InfectionsEnterotoxinsFecesFemaleHumansImmunoassayMaleMiddle AgedBacterial ProteinsBacterial ToxinsEnterotoxinstcdA protein, Clostridium difficiletoxB protein, Clostridium difficile

Identifiers

PMID29788296
PMCPMC6293008
OpenAlexW2803664698

What OpenQuestion holds

Textmetadata
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.