Evidence map›Paper›PMID 32546146›Full record

ArticleBMC pulmonary medicine2020

Role of DNA methylation in the association of lung function with body mass index: a two-step epigenetic Mendelian randomisation study.

André F S Amaral, Medea Imboden, Matthias Wielscher, Faisal I Rezwan, Cosetta Minelli, Judith Garcia-Aymerich, Gabriela P Peralta, Juha Auvinen, Ayoung Jeong, Emmanuel Schaffner and 6 more

Open access · goldAbstract read
In one paragraph

Article in BMC pulmonary medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 43% 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

3 citing papers in PubMed, 5 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

16 authors at 6 institutions in 5 countries.

André F S AmaralNational Heart and Lung Institute, Imperial College London, London, UK. a.amaral@imperial.ac.uk.ORCID http://orcid.org/0000-0002-0369-9449
Medea ImbodenSwiss Tropical and Public Health Institute, Basel, Switzerland.
Matthias WielscherEpidemiology and Biostatistics, School of Public Health, Imperial College London, London, UK.
Faisal I RezwanHuman Development and Health, Faculty of Medicine, University of Southampton, Southampton, UK.
Cosetta MinelliNational Heart and Lung Institute, Imperial College London, London, UK.
Judith Garcia-AymerichISGlobal, Barcelona, Spain.
Gabriela P PeraltaISGlobal, Barcelona, Spain.
Juha AuvinenFaculty of Medicine, University of Oulu, Oulu, Finland.
Ayoung JeongSwiss Tropical and Public Health Institute, Basel, Switzerland.
Emmanuel SchaffnerSwiss Tropical and Public Health Institute, Basel, Switzerland.
Anna Beckmeyer-BorowkoSwiss Tropical and Public Health Institute, Basel, Switzerland.
John W HollowayHuman Development and Health, Faculty of Medicine, University of Southampton, Southampton, UK.
Marjo-Riitta JarvelinEpidemiology and Biostatistics, School of Public Health, Imperial College London, London, UK.
Nicole M Probst-HenschSwiss Tropical and Public Health Institute, Basel, Switzerland.
Deborah L JarvisNational Heart and Lung Institute, Imperial College London, London, UK.
ALEC consortium
Swiss Tropical and Public Health Institute · CHImperial College London · GBUniversitat Pompeu Fabra · ESUniversity of Southampton · GBLung Institute · USUniversity of Oulu · FI

Funding

Medical Research Council G0600705Medical Research Council G1002319Medical Research Council MC_PC_17228Medical Research Council MC_PC_19009Medical Research Council MC_QA137853Medical Research Council MR/S019669/1
6 · The paper itself

Abstract

backgroundLow lung function has been associated with increased body mass index (BMI). The aim of this study was to investigate whether the effect of BMI on lung function is mediated by DNA methylation.

methodsWe used individual data from 285,495 participants in four population-based cohorts: the European Community Respiratory Health Survey, the Northern Finland Birth Cohort 1966, the Swiss Study on Air Pollution and Lung Disease in Adults, and the UK Biobank. We carried out Mendelian randomisation (MR) analyses in two steps using a two-sample approach with SNPs as instrumental variables (IVs) in each step. In step 1 MR, we estimated the causal effect of BMI on peripheral blood DNA methylation (measured at genome-wide level) using 95 BMI-associated SNPs as IVs. In step 2 MR, we estimated the causal effect of DNA methylation on FEV

resultsIn step 1, we found that BMI might have a small causal effect on DNA methylation levels (less than 1% change in methylation per 1 kg/m2 increase in BMI) at two CpGs (cg09046979 and cg12580248). In step 2, we found no evidence of a causal effect of DNA methylation at cg09046979 on lung function. We could not estimate the causal effect of DNA methylation at cg12580248 on lung function as we could not find publicly available data on the association of this CpG with SNPs.

conclusionsTo our knowledge, this is the first paper to report the use of a two-step MR approach to assess the role of DNA methylation in mediating the effect of a non-genetic factor on lung function. Our findings do not support a mediating effect of DNA methylation in the association of lung function with BMI.

Indexed as

Body Mass IndexDNA MethylationAgedCpG IslandsCross-Sectional StudiesFemaleFinlandForced Expiratory VolumeGenome-Wide Association StudyHumansLinear ModelsLungMaleMendelian Randomization AnalysisMiddle AgedPolymorphism, Single NucleotideBody mass indexDNA methylationEffect mediationLung functionMendelian randomisation

Identifiers

PMID32546146
PMCPMC7298775
OpenAlexW3034543382

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Registered trials

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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.