Evidence map›Paper›PMID 27693863›Full record

ReviewJournal of global antimicrobial resistance2016

Host response to Clostridium difficile infection: Diagnostics and detection.

Elena A Usacheva, Jian-P Jin, Lance R Peterson

Open access · greenAbstract readReview
In one paragraph

Review in Journal of global antimicrobial resistance, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

14 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Diagnostic Guidance for C. difficile Infections.Advances in experimental medicine and biology · 2024
    Article
  4. Prophage Carriage and Genetic Diversity within Environmental Isolates ofInternational journal of molecular sciences · 2023
    Article
  5. Microorganisms · 2023
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. The largely unnoticed spread ofInfection prevention in practice · 2020
    Review
  11. Article
  12. Cytoskeletal Tropomyosin as a Biomarker inJournal of clinical medicine research · 2019
    Article
  13. Fecal calprotectin concentrations in cancer patients with Clostridium difficile infection.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2018
    Article
  14. Article
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

3 authors at 3 institutions in 1 country.

Elena A UsachevaInfectious Disease Research, NorthShore University HealthSystem, 2650 Ridge Ave., Evanston, IL 60201, USA; University of Chicago Pritzker School of Medicine, Chicago, IL, USA. Electronic address: EUsacheva@northshore.org.
Jian-P JinDepartment of Physiology, Wayne State University School of Medicine, Detroit, MI 48201, USA.
Lance R PetersonInfectious Disease Research, NorthShore University HealthSystem, 2650 Ridge Ave., Evanston, IL 60201, USA; University of Chicago Pritzker School of Medicine, Chicago, IL, USA.
NorthShore University HealthSystem · USUniversity of Chicago · USWayne State University · US

Funding

Detection of Host Response In Clostridium Difficile InfectionR21AI116659 · NIAID · ENDEAVOR HEALTH CLINICAL OPERATIONS · PI JIN, JIAN-PING, USACHEVA, ELENA ANATOLIEVNA · 2015 to 2016
$437k
NIAID NIH HHS R21 AI116659
6 · The paper itself

Abstract

Clostridium difficile infection (CDI) is a significant healthcare concern worldwide, and C. difficile is recognised as the most frequent aetiological agent of infectious healthcare-associated diarrhoea in hospitalised adult patients. The clinical manifestation of CDI varies from self-limited diarrhoea to life-threatening colitis. Such a broad disease spectrum can be explained by the impact of host factors. Currently, a complex CDI aetiology is widely accepted, acknowledging the interaction between bacteria and the host. C. difficile strains producing clostridial toxins A and B are considered toxigenic and can cause disease; those not producing the toxins are non-pathogenic. A person colonised with a toxigenic strain will not necessarily develop CDI. It is imperative to recognise patients with active disease from those only colonised with this pathogen and to implement appropriate treatment. This can be achieved by diagnostics that rely on host factors specific to CDI. This review will focus on major aspects of CDI pathogenesis and molecular mechanisms, describing host factors in disease progression and assessment of the host response in order to facilitate the development of CDI-specific diagnostics.

Indexed as

Host-Pathogen InteractionsClostridioides difficileClostridium InfectionsColitisDiarrheaHumansRisk FactorsBiomarkerCDIClostridium difficile infectionDiagnosticsHost responsePathogenesis

Identifiers

PMID27693863
PMCPMC5124533
OpenAlexW2522782947

What OpenQuestion holds

Textmetadata
LicenceTDM
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.