Evidence map›Paper›PMID 30623075›Full record

ArticleHealth science reports2018

Sari Törmänen, Johanna Teräsjärvi, Eero Lauhkonen, Merja Helminen, Petri Koponen, Matti Korppi, Kirsi Nuolivirta, Qiushui He

Open access · goldAbstract read
In one paragraph

Article in Health science reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 30% 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, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Health science reports · 2018
    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

8 authors at 3 institutions in 2 countries.

Sari TörmänenCenter for Child Health Research Tampere University and University Hospital Tampere Finland.ORCID 0000-0001-7918-3652
Johanna TeräsjärviDepartment of Medical Microbiology and Immunology Turku University Turku Finland.
Eero LauhkonenCenter for Child Health Research Tampere University and University Hospital Tampere Finland.
Merja HelminenCenter for Child Health Research Tampere University and University Hospital Tampere Finland.
Petri KoponenCenter for Child Health Research Tampere University and University Hospital Tampere Finland.
Matti KorppiCenter for Child Health Research Tampere University and University Hospital Tampere Finland.
Kirsi NuolivirtaDepartment of Pediatrics Seinäjoki Central Hospital Seinäjoki Finland.ORCID 0000-0002-2612-9449
Qiushui HeDepartment of Medical Microbiology and Immunology Turku University Turku Finland.
Tampere University Hospital · FIUniversity of Turku · FISeinäjoki University of Applied Sciences · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimBronchiolitis is a leading cause of hospitalization in infants and is associated with a risk of subsequent asthma. The innate immunity genes, such as those encoding toll-like receptors (TLRs), are likely to play a role in bronchiolitis and post-bronchiolitis outcome. Thus far, only one study has considered TLR5 genes in respiratory syncytial virus (RSV) bronchiolitis. The aim of this study was to investigate the association of TLR5 gene polymorphism with virus etiology and severity of bronchiolitis, and with post-bronchiolitis asthma.

methodsWe recruited 164 infants (age < 6 months) hospitalized for bronchiolitis in this study and determined TLR5 rs5744174 (C > T) single nucleotide polymorphism, virus etiology and severity markers of bronchiolitis, and presence of post-bronchiolitis asthma until age 11 to 13 years.

resultsRSV was detected in 113 (68.9%), rhinovirus in 19 (11.6%), and some other virus in 20 (12.2%) cases. Non-RSV etiology was more common among infants with the variant CT or TT genotype in the TLR5 rs5744174 gene than in those with the CC genotype (89.7% vs 71.7%, P = 0.03). TLR5 rs5744174 polymorphism was not associated with the need of supplementary oxygen or feeding support, with the length of hospital stay, or with post-bronchiolitis asthma at any age.

conclusionThe TLR5 rs5744174 variant genotype may increase the susceptibility to bronchiolitis not caused by RSV.

Indexed as

innate immunityrespiratory syncytial virussingle nucleotide polymorphismToll‐like receptor 5

Identifiers

PMID30623075
PMCPMC6266536
OpenAlexW2804056740

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.