Evidence map›Paper›PMID 36255742›Full record

ArticleHuman molecular genetics2023

FGF20 and PGM2 variants are associated with childhood asthma in family-based whole-genome sequencing studies.

Julian Hecker, Sung Chun, Ahmad Samiei, Cuining Liu, Cecelia Laurie, Priyadarshini Kachroo, Sharon M Lutz, Sanghun Lee, Albert V Smith, Jessica Lasky-Su and 12 more

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Article in Human molecular genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 41% 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

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 3 citations in OpenAlex.

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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

22 authors at 9 institutions in 3 countries.

Julian HeckerChanning Division of Network Medicine, Brigham and Women's Hospital, Boston, MA 02115, USA.ORCID 0000-0001-7918-089X
Sung ChunDivision of Pulmonary Medicine, Boston Children's Hospital, Boston, MA 02115, USA.
Ahmad SamieiDivision of Pulmonary Medicine, Boston Children's Hospital, Boston, MA 02115, USA.
Cuining LiuDivision of Pulmonary Sciences and Critical Care Medicine, School of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Cecelia LaurieDepartment of Biostatistics, University of Washington, Seattle, WA 98195, USA.
Priyadarshini KachrooChanning Division of Network Medicine, Brigham and Women's Hospital, Boston, MA 02115, USA.
Sharon M LutzHarvard Medical School, Boston, MA 02115, USA.
Sanghun LeeDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA 02115, USA.
Albert V SmithDepartment of Biostatistics, University of Michigan, Ann Arbor, MI 48109, USA.
Jessica Lasky-SuChanning Division of Network Medicine, Brigham and Women's Hospital, Boston, MA 02115, USA.
Michael H ChoChanning Division of Network Medicine, Brigham and Women's Hospital, Boston, MA 02115, USA.
Sunita SharmaDivision of Pulmonary Sciences and Critical Care Medicine, School of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Manuel Enrique Soto QuirósDepartment of Pediatrics, Hospital Nacional de Niños, 10101 San José, Costa Rica.
Lydiana AvilaDepartment of Pediatrics, Hospital Nacional de Niños, 10101 San José, Costa Rica.
Juan C CeledónDivision of Pediatric Pulmonary Medicine, UPMC Children's Hospital of Pittsburgh, University of Pittsburgh, Pittsburgh, PA 15224, USA.ORCID 0000-0002-6139-5320
Benjamin RabyHarvard Medical School, Boston, MA 02115, USA.
Xiaobo ZhouChanning Division of Network Medicine, Brigham and Women's Hospital, Boston, MA 02115, USA.
Edwin K SilvermanChanning Division of Network Medicine, Brigham and Women's Hospital, Boston, MA 02115, USA.
Dawn L DeMeoChanning Division of Network Medicine, Brigham and Women's Hospital, Boston, MA 02115, USA.
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Christoph LangeChanning Division of Network Medicine, Brigham and Women's Hospital, Boston, MA 02115, USA.
Scott T WeissChanning Division of Network Medicine, Brigham and Women's Hospital, Boston, MA 02115, USA.
Brigham and Women's Hospital · USBoston Children's Hospital · USHarvard University · USHospital Nacional de Niños · CRUniversity of Colorado Anschutz Medical Campus · USDankook University · KRUniversity of Michigan · USUniversity of Pittsburgh · USUniversity of Washington · US

Funding

Genetic Epidemiology of COPDU01HL089897 · NHLBI · NATIONAL JEWISH HEALTH · PI CRAPO, JAMES D · 2007 to 2021
$56.9M
Genetic Epidemiology of COPDU01HL089856 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI SILVERMAN, EDWIN K · 2007 to 2021
$20.7M
The Genetic Epidemiology of Asthma in Costa RicaR37HL066289 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI WEISS, SCOTT T · 2007 to 2015
$14.6M
Finding Genomic Profiles of COVID-19 Phenotypes from the EHRU01HG008685 · NHGRI · BRIGHAM AND WOMEN'S HOSPITAL · PI ELIZABETH W KARLSON, Matthew S Lebo · 2015 to 2026
$13.6M
Systems Biology of Airway DiseaseP01HL132825 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI DEMEO, DAWN L · 2016 to 2020
$12.6M
Physics of collective cellular migration in lung health and diseaseP01HL120839 · NHLBI · HARVARD SCHOOL OF PUBLIC HEALTH · PI FREDBERG, JEFFREY J · 2014 to 2018
$12.2M
Studies of Rare Genetic Variation in the Isolated Population of SardiniaR01HL117626 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ABECASIS, GONCALO · 2013 to 2016
$10.5M
Rare variants and NHLBI traits in deeply phenotyped cohortsR01HL120393 · NHLBI · UNIVERSITY OF WASHINGTON · PI PSATY, BRUCE M, RICE, KENNETH M. · 2014 to 2016
$8.9M
Integrative Metabolomics of Asthma SeverityR01HL123915 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI LASKY-SU, JESSICA A · 2014 to 2023
$7.0M
The Integrative Genomics of Acute Asthma ControlR01HL118455 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI MILLSTEIN, JOSHUA, RABY, BENJAMIN ALEXANDER · 2014 to 2024
$6.5M
Rare variants and NHLBI traits in deeply phenotyped cohortsU01HL120393 · NHLBI · UNIVERSITY OF WASHINGTON · PI PSATY, BRUCE M, RICE, KENNETH M. · 2017 to 2018
$5.6M
Omic Determinants of Longitudinal Lung Function in AsthmaR01HL155742 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI LASKY-SU, JESSICA A, MCGEACHIE, MICHAEL JOHN · 2021 to 2025
$3.9M
NHGRI NIH HHS R01 HG008976NHGRI NIH HHS U01 HG008685NHLBI NIH HHS K99 HL159234NHLBI NIH HHS P01 HL120839NHLBI NIH HHS P01 HL132825NHLBI NIH HHS R01 HL117626NHLBI NIH HHS R01 HL118455NHLBI NIH HHS R01 HL120393NHLBI NIH HHS R01 HL123915NHLBI NIH HHS R01 HL125734NHLBI NIH HHS R01 HL141826NHLBI NIH HHS R01 HL148667NHLBI NIH HHS R01 HL155742NHLBI NIH HHS R37 HL066289NHLBI NIH HHS U01 HL089856NHLBI NIH HHS U01 HL089897NHLBI NIH HHS U01 HL120393NIMH NIH HHS R01 MH129337
6 · The paper itself

Abstract

backgroundAsthma is a heterogeneous common respiratory disease that remains poorly understood. The established genetic associations fail to explain the high estimated heritability, and the prevalence of asthma differs between populations and geographic regions. Robust association analyses incorporating different genetic ancestries and whole-genome sequencing data may identify novel genetic associations.

methodsWe performed family-based genome-wide association analyses of childhood-onset asthma based on whole-genome sequencing (WGS) data for the 'The Genetic Epidemiology of Asthma in Costa Rica' study (GACRS) and the Childhood Asthma Management Program (CAMP). Based on parent-child trios with children diagnosed with asthma, we performed a single variant analysis using an additive and a recessive genetic model and a region-based association analysis of low-frequency and rare variants.

resultsBased on 1180 asthmatic trios (894 GACRS trios and 286 CAMP trios, a total of 3540 samples with WGS data), we identified three novel genetic loci associated with childhood-onset asthma: rs4832738 on 4p14 ($P=1.72\ast{10}^{-9}$, recessive model), rs1581479 on 8p22 ($P=1.47\ast{10}^{-8}$, additive model) and rs73367537 on 10q26 ($P=1.21\ast{10}^{-8}$, additive model in GACRS only). Integrative analyses suggested potential novel candidate genes underlying these associations: PGM2 on 4p14 and FGF20 on 8p22.

conclusionOur family-based whole-genome sequencing analysis identified three novel genetic loci for childhood-onset asthma. Gene expression data and integrative analyses point to PGM2 on 4p14 and FGF20 on 8p22 as linked genes. Furthermore, region-based analyses suggest independent potential low-frequency/rare variant associations on 8p22. Follow-up analyses are needed to understand the functional mechanisms and generalizability of these associations.

Indexed as

AsthmaGenome-Wide Association StudyFibroblast Growth FactorsGenetic LociGenetic Predisposition to DiseaseHumansPolymorphism, Single NucleotideWhole Genome SequencingFGF20 protein, humanFibroblast Growth Factors

Identifiers

PMID36255742
PMCPMC9896483
OpenAlexW4306734265

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