Evidence map›Paper›PMID 37122714›Full record

ArticleFrontiers in immunology2023

The nasal microbiome in patients suffering from non-steroidal anti-inflammatory drugs-exacerbated respiratory disease in absence of corticosteroids.

Tina J Bartosik, Nicholas J Campion, Kilian Freisl, David T Liu, Katharina Gangl, Victoria Stanek, Aldine Tu, Petra Pjevac, Bela Hausmann, Julia Eckl-Dorna and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
4.0field-weighted citation impact, top 6% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
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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

11 authors at 3 institutions in 1 country.

Tina J BartosikDepartment of Otorhinolaryngology, General Hospital and Medical University of Vienna, Vienna, Austria.
Nicholas J CampionDepartment of Otorhinolaryngology, General Hospital and Medical University of Vienna, Vienna, Austria.
Kilian FreislDepartment of Otorhinolaryngology, General Hospital and Medical University of Vienna, Vienna, Austria.
David T LiuDepartment of Otorhinolaryngology, General Hospital and Medical University of Vienna, Vienna, Austria.
Katharina GanglDepartment of Otorhinolaryngology, General Hospital and Medical University of Vienna, Vienna, Austria.
Victoria StanekDepartment of Otorhinolaryngology, General Hospital and Medical University of Vienna, Vienna, Austria.
Aldine TuDepartment of Otorhinolaryngology, General Hospital and Medical University of Vienna, Vienna, Austria.
Petra PjevacJoint Microbiome Facility of the Medical University of Vienna and the University of Vienna, Vienna, Austria.
Bela HausmannJoint Microbiome Facility of the Medical University of Vienna and the University of Vienna, Vienna, Austria.
Julia Eckl-DornaDepartment of Otorhinolaryngology, General Hospital and Medical University of Vienna, Vienna, Austria.
Sven SchneiderDepartment of Otorhinolaryngology, General Hospital and Medical University of Vienna, Vienna, Austria.
Medical University of Vienna · ATVienna General Hospital · ATUniversity of Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic rhinosinusitis (CRS) is a chronic inflammatory disease phenotypically classified by the absence (CRSsNP) or presence of nasal polyps (CRSwNP). The latter may also be associated with asthma and hypersensitivity towards non-steroidal anti-inflammatory drugs (NSAID) as a triad termed NSAID-exacerbated respiratory disease (N-ERD). The role of the microbiome in these different disease entities with regard to the underlying inflammatory process and disease burden is yet not fully understood. To address this question, we measured clinical parameters and collected nasal samples (nasal mucosal fluids, microbiome swabs from middle meatus and anterior naris) of patients suffering from CRSsNP (n=20), CRSwNP (n=20) or N-ERD (n=20) as well as from patients without CRS (=disease controls, n=20). Importantly, all subjects refrained from taking local or systemic corticosteroids or immunosuppressants for at least two weeks prior to sampling. The nasal microbiome was analyzed using 16S rRNA gene amplicon sequencing, and levels of 33 inflammatory cytokines were determined in nasal mucosal fluids using the MSD platform. Patients suffering from N-ERD and CRSwNP showed significantly worse smell perception and significantly higher levels of type 2 associated cytokines IL-5, IL-9, Eotaxin and CCL17. Across all 4 patient groups,

Indexed as

MicrobiotaRespiration DisordersRhinitisSinusitisAdrenal Cortex HormonesAnti-Inflammatory Agents, Non-SteroidalChronic DiseaseCytokinesHumansInterleukin-5RNA, Ribosomal, 16SAdrenal Cortex HormonesAnti-Inflammatory Agents, Non-SteroidalCytokinesInterleukin-5RNA, Ribosomal, 16S16S rRNA gene amplicon sequencingaspirin-exacerbated respiratory diseasechronic rhinosinusitisCRSCRSwNPmicrobiomeN-ERD

Identifiers

PMID37122714
PMCPMC10140405
OpenAlexW4365515856

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.