Evidence map›Paper›PMID 26173596›Full record

ArticleBMC pharmacology & toxicology2015

Maternal cadmium, iron and zinc levels, DNA methylation and birth weight.

Adriana C Vidal, Viktoriya Semenova, Thomas Darrah, Avner Vengosh, Zhiqing Huang, Katherine King, Monica D Nye, Rebecca Fry, David Skaar, Rachel Maguire and 4 more

Open access · goldAbstract read
In one paragraph

Article in BMC pharmacology & toxicology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed, 2 pooled it
5.4field-weighted citation impact, top 4% 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

65 citing papers in PubMed, 2 syntheses or guidelines pooled it, 110 citations in OpenAlex.

  1. Pooled it
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  15. The imprinted gene Zac1 regulates steatosis in developmental cadmium-induced nonalcoholic fatty liver disease.Toxicological sciences : an official journal of the Society of Toxicology · 2023
    Article
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5 more citing papers are in PubMed but not listed here.

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

14 authors at 7 institutions in 1 country.

Adriana C VidalDepartment of Surgery, Division of Urology, Cedars-Sinai Medical Center, Los Angeles, CA, 90048, USA. adriana.vidal@cshs.org.
Viktoriya SemenovaDepartment of Biological Sciences, Center for Human Health and the Environment, North Carolina State University, Raleigh, NC, 27695, USA. vika245@gmail.com.
Thomas DarrahDivision of Water, Climate, and the Environment, School of Earth Sciences, The Ohio State University, Columbus, OH, 43210, USA. darrah.24@osu.edu.
Avner VengoshNicholas School of the Environment, Duke University, Research Drive, Durham, NC, 27710, USA. vengosh@duke.edu.
Zhiqing HuangDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, Duke University School of Medicine, Research Drive, Durham, NC, 27710, USA. zhiqing.huang@duke.edu.
Katherine KingEnvironmental Public Health Division, U.S. Environmental Protection Agency, Chapel Hill, NC, 27599, USA. katherine.king@duke.edu.
Monica D NyeDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, Duke University School of Medicine, Research Drive, Durham, NC, 27710, USA. mnye@email.unc.edu.
Rebecca FryDepartment of Environmental Sciences and Engineering, Gillings School of Global Public Health, UNC-Chapel Hill, Chapel Hill, NC, 27599, USA. rfry@unc.edu.
David SkaarDepartment of Biological Sciences, Center for Human Health and the Environment, North Carolina State University, Raleigh, NC, 27695, USA. daskaar@ncsu.edu.
Rachel MaguireDepartment of Biological Sciences, Center for Human Health and the Environment, North Carolina State University, Raleigh, NC, 27695, USA. rlmaguir@ncsu.edu.
Amy MurthaDivision of Maternal Fetal Medicine, Department of Obstetrics and Gynecology, Duke University School of Medicine, Erwin Drive, Durham, NC, 27710, USA. amy.murtha@duke.edu.
Joellen SchildkrautDepartment of Community and Family Medicine and Duke Cancer Institute, Duke University School of Medicine, Erwin Drive, Durham, NC, 27710, USA. joellen.schildkraut@duke.edu.
Susan MurphyDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, Duke University School of Medicine, Research Drive, Durham, NC, 27710, USA. susan.murphy@duke.edu.
Cathrine HoyoDepartment of Biological Sciences, Center for Human Health and the Environment, North Carolina State University, Raleigh, NC, 27695, USA. choyo@ncsu.edu.
Duke University · USNorth Carolina State University · USCedars-Sinai Medical Center · USEast Carolina University · USEnvironmental Protection Agency · USThe Ohio State University · USUniversity of North Carolina at Chapel Hill · US

Funding

STOCHASTIC ANALYSIS OF FLOW AND TRANSPORT PHENOMENAP42ES005948 · NIEHS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI FRY, REBECCA · 1992 to 2017
$45.4M
Cancer Control Education ProgramT32CA057726 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Melissa B Gilkey, Melissa A. Troester · 2017 to 2026
$3.7M
Nutrition, Deregulation of Imprinted GenesR01ES016772 · NIEHS · DUKE UNIVERSITY · PI HOYO, CATHRINE · 2009 to 2013
$3.1M
NCI NIH HHS T32 CA057726NICHD NIH HHS N01-HD-5-3422NIEHS NIH HHS ES005948NIEHS NIH HHS ES016772NIEHS NIH HHS P42 ES005948NIEHS NIH HHS R01 ES016772
6 · The paper itself

Abstract

backgroundCadmium (Cd) is a ubiquitous and environmentally persistent toxic metal that has been implicated in neurotoxicity, carcinogenesis and obesity and essential metals including zinc (Zn) and iron (Fe) may alter these outcomes. However mechanisms underlying these relationships remain limited.

methodsWe examined whether maternal Cd levels during early pregnancy were associated with offspring DNA methylation at regulatory sequences of genomically imprinted genes and weight at birth, and whether Fe and Zn altered these associations. Cd, Fe and Zn were measured in maternal blood of 319 women ≤ 12 weeks gestation. Offspring umbilical cord blood leukocyte DNA methylation at regulatory differentially methylated regions (DMRs) of 8 imprinted genes was measured using bisulfite pyrosequencing. Regression models were used to examine the relationships among Cd, Fe, Zn, and DMR methylation and birth weight.

resultsElevated maternal blood Cd levels were associated with lower birth weight (p = 0.03). Higher maternal blood Cd levels were also associated with lower offspring methylation at the PEG3 DMR in females (β = 0.55, se = 0.17, p = 0.05), and at the MEG3 DMR in males (β = 0.72, se = 0.3, p = 0.08), however the latter association was not statistically significant. Associations between Cd and PEG3 and PLAGL1 DNA methylation were stronger in infants born to women with low concentrations of Fe (p < 0.05).

conclusionsOur data suggest the association between pre-natal Cd and offspring DNA methylation at regulatory sequences of imprinted genes may be sex- and gene-specific. Essential metals such as Zn may mitigate DNA methylation response to Cd exposure. Larger studies are required.

Indexed as

AdultBirth WeightCadmiumDNA MethylationDrug InteractionsFemaleFetal BloodFolic AcidHumansInfantIronMaleMaternal ExposurePregnancyRegulatory Sequences, Nucleic AcidYoung AdultCadmiumFolic AcidIronZinc

Identifiers

PMID26173596
PMCPMC4502530
OpenAlexW1521857631

What OpenQuestion holds

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LicenceCC BY
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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.