Evidence map›Paper›PMID 34172473›Full record

ArticleThe European respiratory journal2022

Genetically increased circulating FUT3 level leads to reduced risk of idiopathic pulmonary fibrosis: a Mendelian randomisation study.

Tomoko Nakanishi, Agustin Cerani, Vincenzo Forgetta, Sirui Zhou, Richard J Allen, Olivia C Leavy, Masaru Koido, Deborah Assayag, R Gisli Jenkins, Louise V Wain and 5 more

Open access · hybridAbstract read
In one paragraph

Article in The European respiratory journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 2 pooled it
2.5field-weighted citation impact, top 10% 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

13 citing papers in PubMed, 2 syntheses or guidelines pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Targeting the CD4Molecular biomedicine · 2026
    Article
  4. Review
  5. Emerging Mechanistic Links Between Fucosylation and Senescence in Lung Diseases.Journal of respiratory biology and translational medicine · 2026
    Article
  6. Article
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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

15 authors at 11 institutions in 4 countries.

Tomoko NakanishiDept of Human Genetics, McGill University, Montréal, QC, Canada.ORCID 0000-0001-9510-5646
Agustin CeraniCentre for Clinical Epidemiology, Dept of Medicine, Lady Davis Institute, Jewish General Hospital, McGill University, Montréal, QC, Canada.ORCID 0000-0002-9633-7796
Vincenzo ForgettaCentre for Clinical Epidemiology, Dept of Medicine, Lady Davis Institute, Jewish General Hospital, McGill University, Montréal, QC, Canada.ORCID 0000-0002-6061-4720
Sirui ZhouCentre for Clinical Epidemiology, Dept of Medicine, Lady Davis Institute, Jewish General Hospital, McGill University, Montréal, QC, Canada.ORCID 0000-0003-4963-0815
Richard J AllenDept of Health Sciences, University of Leicester, Leicester, UK.ORCID 0000-0002-8450-3056
Olivia C LeavyDept of Health Sciences, University of Leicester, Leicester, UK.ORCID 0000-0002-1503-5535
Masaru KoidoDept of Cancer Biology, Institute of Medical Science, The University of Tokyo, Tokyo, Japan.ORCID 0000-0002-0348-0666
Deborah AssayagDept of Medicine, Faculty of Medicine, McGill University, Montréal, QC, Canada.ORCID 0000-0002-2497-9984
R Gisli JenkinsNational Heart and Lung Institute, Imperial College London, London, UK.ORCID 0000-0002-7929-2119
Louise V WainDept of Health Sciences, University of Leicester, Leicester, UK.ORCID 0000-0003-4951-1867
Ivana V YangCenter for Genes, Environment and Health and Dept of Medicine, National Jewish Health, Denver, CO, USA.ORCID 0000-0002-1018-489X
G Mark LathropMcGill Genome Centre and Dept of Human Genetics, McGill University, Montréal, QC, Canada.ORCID 0000-0002-2660-7105
Paul J WoltersDept of Medicine, School of Medicine, University of California, San Francisco, CA, USA.ORCID 0000-0002-3108-6164
David A SchwartzDept of Medicine, School of Medicine, University of Colorado Denver, Aurora, CO, USA.ORCID 0000-0001-6743-8443
J Brent RichardsDept of Human Genetics, McGill University, Montréal, QC, Canada brent.richards@mcgill.ca.ORCID 0000-0002-3746-9086
Jewish General Hospital · CAUniversity of Leicester · GBGuy's and St Thomas' NHS Foundation Trust · GBJapan Society for the Promotion of Science · JPKing's College London · GBMcGill Genome Centre · CAMcGill University Health Centre · CANational Jewish Health · USThe University of Tokyo · JPUniversity of California, San Francisco · USUniversity of Colorado Denver · US

Funding

MULTIDISCIPLINARY RESPIRATORY DISEASES RESEARCH TRAININGT32HL007085 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI ELLEN L BURNHAM, LISA A MAIER · 1985 to 2026
$21.6M
MUC5B, a novel therapeutic target for Idiopathic Pulmonary Fibrosis (IPF)UH3HL123442 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI SCHWARTZ, DAVID ALBERT · 2016 to 2018
$4.8M
Preclinical Pulmonary Fibrosis, an opportune rare disease cohortUH3HL151865 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI SCHWARTZ, DAVID ALBERT · 2022 to 2025
$4.3M
MUC5B, a novel therapeutic target for Idiopathic Pulmonary Fibrosis (IPF)UH2HL123442 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI SCHWARTZ, DAVID ALBERT · 2014 to 2015
$3.0M
Genes and Transcripts that Interact with MUC5B in Pulmonary FibrosisR01HL149836 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI CLOUTHIER, DAVID E., SCHWARTZ, DAVID ALBERT · 2020 to 2023
$3.0M
Colorado StARR Program in Medicine and Pediatrics (CSPMP)R38HL143511 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI Steven Herbert Abman, Peter N. Buttrick · 2020 to 2026
$2.7M
Preclinical Pulmonary Fibrosis, an opportune rare disease cohortUG3HL151865 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI SCHWARTZ, DAVID ALBERT · 2020 to 2021
$1.7M
Colorado Undergraduate Research in Environmental Health SciencesR25ES025476 · NIEHS · UNIVERSITY OF COLORADO DENVER · PI ALISON K BAUER, Jared Michael Brown · 2015 to 2026
$1.3M
Cancer Research UKDepartment of HealthNHLBI NIH HHS R01 HL149836NHLBI NIH HHS R38 HL143511NHLBI NIH HHS T32 HL007085NHLBI NIH HHS UG3 HL151865NHLBI NIH HHS UH2 HL123442NHLBI NIH HHS UH3 HL123442NHLBI NIH HHS UH3 HL151865NIEHS NIH HHS R25 ES025476Wellcome Trust
6 · The paper itself

Abstract

backgroundIdiopathic pulmonary fibrosis (IPF) is a progressive, fatal fibrotic interstitial lung disease. Few circulating biomarkers have been identified to have causal effects on IPF.

methodsTo identify candidate IPF-influencing circulating proteins, we undertook an efficient screen of circulating proteins by applying a two-sample Mendelian randomisation (MR) approach with existing publicly available data. For instruments, we used genetic determinants of circulating proteins which reside

resultsMR analyses of 834 proteins found that a 1 sd increase in circulating galactoside 3(4)-l-fucosyltransferase (FUT3) and α-(1,3)-fucosyltransferase 5 (FUT5) was associated with a reduced risk of IPF (OR 0.81, 95% CI 0.74-0.88; p=6.3×10

conclusionsAn efficient MR scan of 834 circulating proteins provided evidence that genetically increased circulating FUT3 level is associated with reduced risk of IPF.

Indexed as

FucosyltransferasesIdiopathic Pulmonary FibrosisGenome-Wide Association StudyHumansMendelian Randomization AnalysisPolymorphism, Single NucleotideFucosyltransferases

Identifiers

PMID34172473
PMCPMC8828995
OpenAlexW3177396039

What OpenQuestion holds

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LicenceCC BY-NC
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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.