Evidence map›Paper›PMID 31481635›Full record

ArticleThorax2019

β

Truls Sylvan Ingebrigtsen, Jørgen Vestbo, Line Rode, Jacob Louis Marott, Peter Lange, Børge G Nordestgaard

Open access · bronzeAbstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Thorax, 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
1.2field-weighted citation impact, top 19% 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, 9 citations in OpenAlex.

  1. Article
  2. Update on the Role of β2AR and TRPV1 in Respiratory Diseases.International journal of molecular sciences · 2024
    Review
  3. Article
  4. Article
  5. Article
  6. βJournal of clinical medicine · 2019
    Article
  7. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 2 countries.

Truls Sylvan IngebrigtsenDepartment of Respiratory Medicine, Hvidovre Hospital, Hvidovre and Amager Hospital, Copenhagen University Hospital, University of Copenhagen, Copenhagen, Denmark.
Jørgen VestboDivision of Infection, Immunity and Respiratory Medicine, School of Biological Sciences, University of Manchester, Manchester, UK.
Line RodeThe Copenhagen General Population Study, Herlev and Gentofte Hospital, Copenhagen University Hospital, University of Copenhagen, Copenhagen, Denmark.
Jacob Louis MarottThe Copenhagen General Population Study, Herlev and Gentofte Hospital, Copenhagen University Hospital, University of Copenhagen, Copenhagen, Denmark.
Peter LangeDepartment of Respiratory Medicine, Hvidovre Hospital, Hvidovre and Amager Hospital, Copenhagen University Hospital, University of Copenhagen, Copenhagen, Denmark.
Børge G NordestgaardThe Copenhagen General Population Study, Herlev and Gentofte Hospital, Copenhagen University Hospital, University of Copenhagen, Copenhagen, Denmark Boerge.Nordestgaard@regionh.dk.
Copenhagen University Hospital · DKGentofte Hospital · DKAmager Hospital · DKUniversity of Manchester · GB

Funding

Department of Health
6 · The paper itself

Abstract

backgroundIndividual susceptibility to exacerbations in chronic obstructive pulmonary disease (COPD) is likely influenced by genetic factors; however, most such variance is unexplained. We hypothesised that β

methodsAmong 96 762 individuals in the Copenhagen General Population Study, we identified 5262 with COPD (forced expiratory volume in one second divided by forced vital capacity, FEV

resultsWe recorded 461 severe exacerbations in 5262 subjects. The HRs for severe exacerbations were 1.62 (95% CI 1.30 to 2.03, p=0.00002) for 16Gly/Arg heterozygotes and 1.41 (1.04 to 1.91, p=0.03) for 16Arg homozygotes, compared with 16Gly homozygotes. HRs were 1.35 (1.03 to 1.76, p=0.03) for 27Gln/Glu heterozygotes and 1.49 (1.12 to 1.98, p=0.006) for 27Gln homozygotes, compared with 27Glu homozygotes. Similar trends were observed in the CCHS. Among 27Gln homozygotes only, HRs were 5.20 (1.81 to 14.9, p=0.002) for 16Gly/Arg heterozygotes and 4.03 (1.40 to 11.6, p=0.01) for 16Arg homozygotes, compared with 16Gly homozygotes.

conclusionCommon β

Indexed as

ForecastingPolymorphism, GeneticAdultAgedAllelesDisease ProgressionFemaleFollow-Up StudiesForced Expiratory VolumeGenotypeHumansMaleMiddle AgedProspective StudiesPulmonary Disease, Chronic ObstructiveReceptors, Adrenergic, beta-2Receptors, Adrenergic, beta-2adrenoreceptor polymorphismsCOPDprecision medicine

Identifiers

PMID31481635
OpenAlexW2971567547

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.