Evidence map›Paper›PMID 34937578›Full record

ArticleClinical epigenetics2021

DNA methylation mediates the association between breastfeeding and early-life growth trajectories.

Laurent Briollais, Denis Rustand, Catherine Allard, Yanyan Wu, Jingxiong Xu, Samyukta Govinda Rajan, Marie-France Hivert, Myriam Doyon, Luigi Bouchard, Patrick O McGowan and 2 more

Open access · goldAbstract read
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 31 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 2 pooled it
11.0field-weighted citation impact, top 1% 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

31 citing papers in PubMed, 2 syntheses or guidelines pooled it, 44 citations in OpenAlex.

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  13. The interaction of breastfeeding and genetic factors on childhood obesity.European journal of obstetrics & gynecology and reproductive biology: X · 2024
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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

12 authors at 6 institutions in 3 countries.

Laurent BriollaisLunenfeld-Tanenbaum Research Institute, Sinai Health System, 60, Murray street - Room 5-237, Toronto, ON, M5T 3L9, Canada. laurent@lunenfeld.ca.ORCID 0000-0001-5741-9812
Denis RustandLunenfeld-Tanenbaum Research Institute, Sinai Health System, 60, Murray street - Room 5-237, Toronto, ON, M5T 3L9, Canada.
Catherine AllardCentre de Recherche du Centre Hospitalier Universitaire de Sherbrooke (CHUS), Sherbrooke, QC, Canada.
Yanyan WuDepartment of Public Health Sciences, University of Hawai'i at Manoa, Honolulu, HI, USA.
Jingxiong XuLunenfeld-Tanenbaum Research Institute, Sinai Health System, 60, Murray street - Room 5-237, Toronto, ON, M5T 3L9, Canada.
Samyukta Govinda RajanDalla Lana School of Public Health, University of Toronto, Toronto, ON, Canada.
Marie-France HivertDivision of Chronic Disease Research Across the Life Course, Department of Population Medicine, Harvard Pilgrim Health Care Institute, Harvard Medical School, Boston, MA, 02215, USA.
Myriam DoyonCentre de Recherche du Centre Hospitalier Universitaire de Sherbrooke (CHUS), Sherbrooke, QC, Canada.
Luigi BouchardDepartment of Medical Biology, CIUSSS Saguenay-Lac-Saint-Jean, Hôpital Universitaire de Chicoutimi, Saguenay, QC, G7H 5H6, Canada.
Patrick O McGowanDepartment of Biological Sciences, University of Toronto - Scarborough, Toronto, ON, Canada.
Steven MatthewsLunenfeld-Tanenbaum Research Institute, Sinai Health System, 60, Murray street - Room 5-237, Toronto, ON, M5T 3L9, Canada.
Steven LyeLunenfeld-Tanenbaum Research Institute, Sinai Health System, 60, Murray street - Room 5-237, Toronto, ON, M5T 3L9, Canada.
Lunenfeld-Tanenbaum Research Institute · CAUniversity of Toronto · CACentre Hospitalier Universitaire de Sherbrooke · CAUniversité de Sherbrooke · CAInserm · FRUniversity of Hawaiʻi at Mānoa · US

Funding

Epigenetic Pathways to Conduct Problem Trajectories: Early Environmental RisksR01HD068437 · NICHD · KING'S COLLEGE LONDON · PI BARKER, EDWARD D., MILL, JONATHAN · 2012 to 2014
$1.1M
Biotechnology and Biological Sciences Research Council BB/I025263/1Biotechnology and Biological Sciences Research Council BBI025751/1Canadian Institute of Health Research MOP 115071CIHR PJT-152989Medical 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_12013/8NICHD NIH HHS R01 HD068437Wellcome TrustWellcome Trust 076467/Z/05/Z
6 · The paper itself

Abstract

backgroundThe role of breastfeeding in modulating epigenetic factors has been suggested as a possible mechanism conferring its benefits on child development but it lacks evidence. Using extensive DNA methylation data from the ALSPAC child cohort, we characterized the genome-wide landscape of DNA methylation variations associated with the duration of exclusive breastfeeding and assessed whether these variations mediate the association between exclusive breastfeeding and BMI over different epochs of child growth.

resultsExclusive breastfeeding elicits more substantial DNA methylation variations during infancy than at other periods of child growth. At the genome-wide level, 13 CpG sites in girls (miR-21, SNAPC3, ATP6V0A1, DHX15/PPARGC1A, LINC00398/ALOX5AP, FAM238C, NATP/NAT2, CUX1, TRAPPC9, OSBPL1A, ZNF185, FAM84A, PDPK1) and 2 CpG sites in boys (IL16 and NREP), mediate the association between exclusive breastfeeding and longitudinal BMI. We found enrichment of CpG sites located within miRNAs and key pathways (AMPK signaling pathway, insulin signaling pathway, endocytosis). Overall DNA methylation variation corresponding to 3 to 5 months of exclusive breastfeeding was associated with slower BMI growth the first 6 years of life compared to no breastfeeding and in a dose-response manner with exclusive breastfeeding duration.

conclusionsOur study confirmed the early postnatal period as a critical developmental period associated with substantial DNA methylation variations, which in turn could mitigate the development of overweight and obesity from infancy to early childhood. Since an accelerated growth during these developmental periods has been linked to the development of sustained obesity later in life, exclusive breastfeeding could have a major role in preventing the risks of overweight/obesity and children and adults through DNA methylation mechanisms occurring early in life.

Indexed as

Age FactorsBody Mass IndexBreast FeedingChildChild, PreschoolCorrelation of DataDNA MethylationFemaleGenome-Wide Association StudyGrowth DisordersHumansMaleALSPACBMIBreastfeedingChild cohortDNA methylationDOHaDMediationmicroRNAObesity

Identifiers

PMID34937578
PMCPMC8697471
OpenAlexW4200427615

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.