Evidence map›Paper›PMID 30252029›Full record

ArticleJournal of Crohn's & colitis2019

Sexual Dimorphism in the Response to Broad-spectrum Antibiotics During T Cell-mediated Colitis.

Christy A Harrison, Daniel Laubitz, Monica T Midura-Kiela, Deepa R Jamwal, David G Besselsen, Fayez K Ghishan, Pawel R Kiela

Open access · bronzeAbstract read
In one paragraph

Article in Journal of Crohn's & colitis, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Antibiotic perturbations to the gut microbiome.Nature reviews. Microbiology · 2023
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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

7 authors at 2 institutions in 1 country.

Christy A HarrisonDepartment of Pediatrics, Steele Children's Research Center, Tucson, AZ, USA.
Daniel LaubitzDepartment of Pediatrics, Steele Children's Research Center, Tucson, AZ, USA.
Monica T Midura-KielaDepartment of Pediatrics, Steele Children's Research Center, Tucson, AZ, USA.
Deepa R JamwalDepartment of Pediatrics, Steele Children's Research Center, Tucson, AZ, USA.
David G BesselsenUniversity Animal Care, University of Arizona, Tucson, AZ, USA.
Fayez K GhishanDepartment of Pediatrics, Steele Children's Research Center, Tucson, AZ, USA.
Pawel R KielaDepartment of Pediatrics, Steele Children's Research Center, Tucson, AZ, USA.
Children's Center · USUniversity of Arizona · US

Funding

DEVELOPMENT OF INTESTINAL ION TRANSPORTR01DK041274 · NIDDK · VANDERBILT UNIVERSITY · PI GHISHAN, FAYEZ KHALAF, KIELA, PAWEL R · 1988 to 2016
$5.5M
Modulation of dendritic cell function in the pathogenesis of Inflammatory Bowel DiseasesR01DK109711 · NIDDK · UNIVERSITY OF ARIZONA · PI GHISHAN, FAYEZ KHALAF, KIELA, PAWEL R · 2016 to 2020
$1.7M
NIDDK NIH HHS R01 DK041274NIDDK NIH HHS R01 DK109711
6 · The paper itself

Abstract

backgroundBroad-spectrum antibiotics [Abx], including combination therapy with ciprofloxacin and metronidazole, are often prescribed during the treatment of inflammatory bowel disease [IBD] to alleviate symptoms, but with varying success. In this pilot study, we studied the effects of Abx on the course of experimental colitis, with a particular focus on sex as a determinant of the microbial and inflammatory responses.

methodsThe effects of Abx were tested on colonic inflammation and microbiome in male and female Rag-/- mice, using adoptive transfer of naïve T cells to induce colitis in a short-term [2-week] and long-term [9-week] study.

resultsWe observed disparities between the sexes in both the response to adoptive T cell transfer and the effects of Abx. At baseline without Abx, female mice displayed a trend toward a more severe colitis than males. In both the short- and the long-term experiments, gut microbiota of some female mice exposed to Abx showed weak, delayed, or negligible shifts. Caecum weight was significantly lower in Abx-treated females. Abx exposure favoured a quick and persistent rise in Enterococcaceae exclusively in females. Males had higher relative abundance of Lactobacillaceae following Abx exposure relative to females. Abx-treated females trended toward higher colitis scores than Abx-treated males, and towards higher levels of IL-17A, NOS2, and IL-22.

conclusionsAlthough preliminary, our results suggest a differential response to both inflammation and Abx between male and female mice, The findings may be relevant to current practice and also as the basis for further studies on the differential gender effects during long-term antibiotic exposure in IBD.

Indexed as

Adoptive TransferSex FactorsAnimalsAnti-Bacterial AgentsCD4-Positive T-LymphocytesCecumCiprofloxacinColitisDNA-Binding ProteinsEnterococcaceaeFemaleGastrointestinal MicrobiomeGene ExpressionInterleukin-17Interleukin-22InterleukinsAnti-Bacterial AgentsCiprofloxacinDNA-Binding ProteinsIl17a protein, mouseInterleukin-17Interleukin-22InterleukinsMetronidazoleNitric Oxide Synthase Type IINos2 protein, mouseRag2 protein, mouseRNA, Messenger

Identifiers

PMID30252029
PMCPMC6302957
OpenAlexW2893091879

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.