Evidence map›Paper›PMID 31758685›Full record

ArticleJournal of Crohn's & colitis2020

Decreased Enteric Bacterial Composition and Diversity in South American Crohn's Disease Vary With the Choice of Treatment Strategy and Time Since Diagnosis.

Angélica Cruz-Lebrón, Leticia D'argenio Garcia, Aarthi Talla, Samira Joussef-Piña, Miguel E Quiñones-Mateu, Rafick-Pierre Sékaly, Karina Inacio Ladislau de Carvalho, Alan D Levine

Open access · greenAbstract read
In one paragraph

Article in Journal of Crohn's & colitis, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 29% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
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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

8 authors at 3 institutions in 3 countries.

Angélica Cruz-LebrónDepartment of Molecular Biology and Microbiology, Case Western Reserve University, Cleveland, OH, USA.
Leticia D'argenio GarciaHospital Israelita Albert Einstein, São Paulo, Brazil.
Aarthi TallaDepartment of Pathology, Case Western Reserve University, Cleveland, OH, USA.
Samira Joussef-PiñaDepartment of Pathology, Case Western Reserve University, Cleveland, OH, USA.
Miguel E Quiñones-MateuDepartment of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.
Rafick-Pierre SékalyDepartment of Pathology, Case Western Reserve University, Cleveland, OH, USA.
Karina Inacio Ladislau de CarvalhoHospital Israelita Albert Einstein, São Paulo, Brazil.
Alan D LevineDepartment of Molecular Biology and Microbiology, Case Western Reserve University, Cleveland, OH, USA.
Case Western Reserve University · USHospital Israelita Albert Einstein · BRUniversity of Otago · NZ

Funding

WG3: HIV, Co-infections and Co-morbiditiesP30AI036219 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI Sharon L. Hillier, JONATHAN KARN · 1994 to 2026
$50.0M
Identification of immune protective pathways dysregulated by opioid use in HIV infection, using a systems biology-based approach, toward the goal of pharmacological restoration of immune functionR01DA043253 · NIDA · CASE WESTERN RESERVE UNIVERSITY · PI LEVINE, ALAN DAVID · 2016 to 2021
$4.3M
Repairing the intestinal epithelium from the dual action of HIV and drug useDP1DA037997 · NIDA · CASE WESTERN RESERVE UNIVERSITY · PI LEVINE, ALAN DAVID · 2015 to 2019
$4.1M
NIAID NIH HHS P30 AI036219NIDA NIH HHS DP1 DA037997NIDA NIH HHS R01 DA043253
6 · The paper itself

Abstract

BACKGROUND AND

aimsThe symptomology of Crohn's disease [CD], a chronic inflammatory disease of the digestive tract, correlates poorly with clinical, endoscopic or immunological assessments of disease severity. The prevalence of CD in South America is rising, reflecting changes in socio-economic stability. Many treatment options are available to CD patients, including biological agents and corticosteroids, each of which offers variable efficacy attributed to host genetics and environmental factors associated with alterations in the gut microbiota.

methodsBased on 16S rRNA gene sequencing and taxonomic differences, we compared the faecal microbial population of Brazilian patients with CD treated with corticosteroid or anti-tumour necrosis factor [anti-TNF] immunotherapy. Faecal calprotectin and plasma sCD14 levels were quantified as markers for local and systemic inflammation, respectively.

resultsAnti-TNF treatment led to an increased relative abundance of Proteobacteria and a decreased level of Bacteroidetes. In contrast, corticoid treatment was associated with an increase in the relative abundance of Actinobacteria, which has been linked to inflammation in CD. Disruption of the faecal microbiota was related to decreased bacterial diversity and composition. Moreover, the choice of clinical regimen and time since diagnosis modulate the character of the resulting dysbiosis.

conclusionsEnteric microbial populations in CD patients who have been treated are modulated by disease pathogenesis, local inflammatory microenvironment and treatment strategy. The dysbiosis that remains after anti-TNF treatment due to decreased bacterial diversity and composition abates restoration of the microbiota to a healthy state, suggesting that the identification and development of new clinical treatments for CD must include their capacity to normalize the gut microbiota.

Indexed as

Crohn DiseaseDysbiosisBrazilFecesGastrointestinal MicrobiomeGlucocorticoidsHumansIntestinal MucosaLeukocyte L1 Antigen ComplexLipopolysaccharide ReceptorsMalePrevalenceRNA, Ribosomal, 16SSeverity of Illness IndexTumor Necrosis Factor InhibitorsGlucocorticoidsLeukocyte L1 Antigen ComplexLipopolysaccharide ReceptorsRNA, Ribosomal, 16STumor Necrosis Factor Inhibitorsanti-TNFcorticoidsMicrobiome

Identifiers

PMID31758685
PMCPMC7346893
OpenAlexW2990360308

What OpenQuestion holds

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Registered trials

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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.