Evidence map›Paper›PMID 32282124›Full record

Observational studyInternational forum of allergy & rhinology2020

Cystic fibrosis transmembrane conductance regulator function, not TAS2R38 gene haplotypes, predict sinus surgery in children and young adults with cystic fibrosis.

Nicholas M Dalesio, Melis A Aksit, Kwangmi Ahn, Karen S Raraigh, Joseph M Collaco, Sharon McGrath-Morrow, Pamela L Zeitlin, Steven S An, Garry R Cutting

Open access · greenAbstract readObservational StudyTwin Study
In one paragraph

Observational study in International forum of allergy & rhinology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.8field-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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. 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

9 authors at 4 institutions in 2 countries.

Nicholas M DalesioDivision of Pediatric Anesthesia/Critical Care Medicine, Department of Anesthesiology and Critical Care Medicine, Johns Hopkins University, Baltimore, MD.ORCID 0000-0003-4375-2651
Melis A AksitMcKusick-Nathans Institute of the Department of Genetic Medicine, Johns Hopkins University, Baltimore, MD.
Kwangmi AhnGenetic Epidemiology Research Branch, National Institute of Mental Health, Bethesda, MD.
Karen S RaraighMcKusick-Nathans Institute of the Department of Genetic Medicine, Johns Hopkins University, Baltimore, MD.
Joseph M CollacoDepartment of Pediatric Pulmonology, Johns Hopkins University, Baltimore, MD.
Sharon McGrath-MorrowDepartment of Pediatric Pulmonology, Johns Hopkins University, Baltimore, MD.
Pamela L ZeitlinDepartment of Pediatrics, National Jewish Health, Denver, CO.
Steven S AnDepartment of Pharmacology, Rutgers-Robert Wood Johnson Medical School, The State University of New Jersey, Piscataway, NJ.
Garry R CuttingMcKusick-Nathans Institute of the Department of Genetic Medicine, Johns Hopkins University, Baltimore, MD.
Johns Hopkins University · USNational Institute of Mental Health · USNational Jewish Health · USRutgers, The State University of New Jersey · US

Funding

New Jersey Alliance for Clinical Translational Science: NJ ACTSUL1TR003017 · NCATS · RUTGERS BIOMEDICAL/HEALTH SCIENCES-RBHS · PI PANETTIERI, REYNOLD ALEXANDER · 2019 to 2023
$28.9M
Project 4 - OGR1- and TSPO- dependent mechanisms mediated by benzodiazepines affecting ASM contractionP01HL114471 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI BENOVIC, JEFFREY L · 2013 to 2023
$23.9M
Resolution of Diffuse Inflammatory Lung Injury in Neonatal MiceR01HL114800 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI MCGRATH-MORROW, SHARON ANN · 2013 to 2021
$3.3M
Gene-Environment Interactions in Cystic Fibrosis Lung DiseaseR01HL128475 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI COLLACO, JOSEPH MICHAEL · 2016 to 2019
$1.1M
NCATS NIH HHS UL1 TR003017NHLBI NIH HHS P01 HL114471NHLBI NIH HHS R01 HL114800NHLBI NIH HHS R01 HL128475
6 · The paper itself

Abstract

backgroundChronic rhinosinusitis symptomatology begins in early childhood individuals with cystic fibrosis (CF). Cystic fibrosis transmembrane conductance regulator (CFTR) function contributes to sinus development and disease. Genetic variants of the bitter taste receptor TAS2R38 have been suggested to contribute to sinus disease severity in individuals without CF. Our objective was to explore whether functional TAS2R38 haplotypes and CFTR function are associated with sinus disease or the need for sinus surgery in individuals with CF.

methodsWe conducted a retrospective study using prospectively collected data from the CF Twin-Sibling Study. The function of CFTR was assessed via chloride conductance. Genotyping of the TAS2R38 gene identified patients who were homozygous for the functional haplotype, heterozygous, or homozygous for nonfunctional haplotypes. Clustered multivariate logistic regression was performed, controlling for sex and family relationship.

resultsA total of 1291 patients were evaluated. Patients with ≤1% CFTR function were 1.56 times more likely to require sinus surgery than those with >1% CFTR function (p = 0.049). CFTR function did not correlate significantly with the presence of sinus disease (p = 0.30). In addition, there were no statistically significant differences in diagnosis of sinus disease or need for sinus surgery between patients with functional and nonfunctional TAS2R38 haplotypes.

conclusionCFTR function correlates with need for sinus surgery, whereas TAS2R38 function does not appear to contribute to sinus disease or the need for sinus surgery in patients with CF.

Indexed as

Cystic FibrosisSinusitisAdolescentAdultChildChild, PreschoolCystic Fibrosis Transmembrane Conductance RegulatorFemaleHaplotypesHumansInfantMaleMiddle AgedNasal Surgical ProceduresParanasal SinusesReceptors, G-Protein-CoupledCFTR protein, humanCystic Fibrosis Transmembrane Conductance RegulatorReceptors, G-Protein-CoupledTaste Receptors, Type 2bitter taste receptorCFTR functioncystic fibrosissinusitisTAS2R38

Identifiers

PMID32282124
PMCPMC7266728
OpenAlexW3015671329

What OpenQuestion holds

Textmetadata
LicenceTDM
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.