Evidence map›Paper›PMID 33407823›Full record

ArticleClinical epigenetics2021

Pre-adolescence DNA methylation is associated with lung function trajectories from pre-adolescence to adulthood.

Shadia Khan Sunny, Hongmei Zhang, Fawaz Mzayek, Caroline L Relton, Susan Ring, A John Henderson, Susan Ewart, John W Holloway, S Hasan Arshad

Open access · goldAbstract readComparative Study
In one paragraph

Article in Clinical epigenetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

8 citing papers in PubMed, 15 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Review
  6. Exposure to PMAnnals of the American Thoracic Society · 2022
    Article
  7. 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

9 authors at 4 institutions in 2 countries.

Shadia Khan SunnyDivision of Epidemiology, Biostatistics, and Environmental Health Sciences, School of Public Health, University of Memphis, Memphis, TN, 38152, USA.
Hongmei ZhangDivision of Epidemiology, Biostatistics, and Environmental Health Sciences, School of Public Health, University of Memphis, Memphis, TN, 38152, USA. hzhang6@memphis.edu.ORCID 0000-0003-3557-0364
Fawaz MzayekDivision of Epidemiology, Biostatistics, and Environmental Health Sciences, School of Public Health, University of Memphis, Memphis, TN, 38152, USA.
Caroline L ReltonMRC Integrative Epidemiology Unit, University of Bristol, Bristol, BS8 2BN, UK.
Susan RingMRC Integrative Epidemiology Unit, University of Bristol, Bristol, BS8 2BN, UK.
A John HendersonPopulation Health Sciences, University of Bristol, Bristol, BS8 2BN, UK.
Susan EwartLarge Animal Clinical Sciences, Michigan State University, East Lansing, MI, USA.
John W HollowayHuman Development and Health, Faculty of Medicine, University of Southampton, Southampton, SO16 6YD, UK.
S Hasan ArshadNIHR Southampton Biomedical Research Centre, University Hospital Southampton, Southampton, SO16 6YD, UK.
University of Bristol · GBUniversity of Memphis · USUniversity Hospital Southampton NHS Foundation Trust · GBMichigan State University · US

Funding

Does epigenetic methylation explain the gender-switch in adolescent asthma?R01AI121226 · NIAID · UNIVERSITY OF MEMPHIS · PI HOLLOWAY, JOHN W, ZHANG, HONGMEI · 2016 to 2020
$3.2M
Effect of Prenatal Compounds on Adult Lung Function via Neonatal DNA MethylationR01HL132321 · NHLBI · UNIVERSITY OF MEMPHIS · PI KARMAUS, WILFRIED JJ · 2016 to 2020
$3.2M
Transgenerational epigenetic inheritance of allergy in a multigenerational cohortR01AI091905 · NIAID · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI KARMAUS, WILFRIED JJ · 2011 to 2015
$2.7M
Epidemiology of asthma: risk and prognosis in a cohort from birth to adolescenceR01HL082925 · NHLBI · ST. MARY'S HOSPITAL NEWPORT · PI ARSHAD, SYED HASAN · 2007 to 2010
$1.7M
Biotechnology and Biological Sciences Research Council BB/I025263/1Biotechnology and Biological Sciences Research Council BBI025751/1Medical Research Council G0401540/73080Medical Research Council G9815508Medical Research Council MC_PC_15018Medical Research Council MC_PC_19009Medical Research Council MC_UU_00011/1Medical Research Council MC_UU_00011/5Medical Research Council MC_UU_12013/1Medical Research Council MC_UU_12013/2Medical Research Council MC_UU_12013/8Medical Research Council MR/M022501/1NHLBI NIH HHS R01 HL082925NHLBI NIH HHS R01 HL132321NIAID NIH HHS R01 AI091905NIAID NIH HHS R01 AI121226Wellcome TrustWellcome Trust 102215/2/13/2
6 · The paper itself

Abstract

backgroundThe pattern of lung function development from pre-adolescence to adulthood plays a significant role in the pathogenesis of respiratory diseases. Inconsistent findings in genetic studies on lung function trajectories, the importance of DNA methylation (DNA-M), and the critical role of adolescence in lung function development motivated the present study of pre-adolescent DNA-M with lung function trajectories. This study investigated epigenome-wide associations of DNA-M at cytosine-phosphate-guanine dinucleotide sites (CpGs) at childhood with lung function trajectories from childhood to young adulthood.

methodsDNA-M was measured in peripheral blood at age 10 years in the Isle of Wight (IOW) birth cohort. Spirometry was conducted at ages 10, 18, and 26 years. A training/testing-based method was used to screen CpGs. Multivariable logistic regressions were applied to assess the association of DNA-M with lung function trajectories from pre-adolescence to adulthood. To detect differentially methylated regions (DMRs) among CpGs, DMR enrichment analysis was conducted. Findings were further tested in the Avon Longitudinal Study of Parents and Children (ALSPAC) cohort. Pathway analyses were performed on the mapped genes of the identified CpGs and DMRs. Biological relevance of the identified CpGs was assessed with gene expression. All analyses were stratified by sex.

resultsHigh and low trajectories of FVC, FEV

conclusionThe identified CpGs at pre-adolescence have the potential to serve as candidate markers for lung function trajectory prediction and chronic lung diseases.

Indexed as

AdolescentAdultAge FactorsChildChild, PreschoolDNA MethylationEnvironmental ExposureEnvironmental PollutantsFemaleGenome-Wide Association StudyHumansInfantInfant, NewbornLongitudinal StudiesLung DiseasesMaleEnvironmental PollutantsAdolescenceALSPAC)COPDDNA methylationEpigenome-wideLung function trajectoryPopulation-based cohorts (IOW birth cohort

Identifiers

PMID33407823
PMCPMC7789734
OpenAlexW3119553843

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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.